Revised List of Miscellaneous Stocks
Chetelat, R. T.
C.M. Rick Tomato Genetics Resource Center, Dept. of Plant Sciences, University of California, Davis, CA 95616
This list of approx. 1,560 miscellaneous genetic stocks is a revision of the previous one issued in TGC 53 (2003). Extinct, obsolete, or faulty accessions have been dropped. New accessions that have been added to the list include a group of ‘provisional mutants’ originating from various sources. These are mostly morphological traits detected in M2’s and later generations from mutagenesis populations. Most are probably monogenic characters, with a few containing multiple mutant loci per line. Also, several new and useful linkage tester stocks, each containing two or more morphological markers on a single chromosome, have been acquired. The new tester stocks represent chromosomes 1, 7, 10 and 11.
We attempt to maintain all listed accessions in adequate seed supply for distribution. However, some stocks, such as certain multiple marker combinations, aneuploids, or prebreds, are weak and require special cultural care; consequently, seed supplies may at times be too low to permit distribution.
Names and phenotypic classes of individual mutations are given in the last Monogenic Stock List (TGC 55); other pertinent data are presented in previous TGC Reports, as cited below. More detailed information on these stocks are available at our website (
http://tgrc.ucdavis.edu), including genotype, phenotype, origin, and recommendations for growth and reproduction.see also:
Wild Species Stocks (1,131 accessions total) are listed in TGC 54 (2004)
Monogenic Stocks (994 accessions total) are listed in TGC 55 (2005)
Types of Stocks on this List
1. Cultivars and Landraces
1.1. Modern and Vintage Cultivars
1.2. Latin American Cultivars
2. Prebred Lines
2.1. Introgression Lines
2.2. Backcross Recombinant Inbreds
2.3. Alien Substitution Lines
2.4. Monosomic Alien Addition Lines
2.5. Other Prebred Lines
3. Stress Tolerant Stocks
4. Cytogenetic Stocks
4.1. Translocations
4.2. Trisomics
4.3. Autotetraploids
5. Cytoplasmic Variants
6. Genetic Marker Combinations
6.1. Chromosome Marker Stocks
6.2. Linkage Screening Testers
6.3. Miscellaneous Marker Combinations
7. Provisional mutants
1. CULTIVARS AND LANDRACES
1.1. Modern and Vintage Cultivars (198)
We maintain the following set of cultivars, inbreds, and breeding lines for various purposes, mainly as isogenic (or nearly isogenic) stocks for specific mutants, standards for genetic comparison, sources of disease resistances, or other purposes. Marglobe is considered the standard for tomato gene (mutant) nomenclature. Most lines have been maintained by selfing for many generations.
|
Accession |
Cultivar |
|
LA0818 |
A-1 |
|
LA0516 |
Ace |
|
LA2838A |
Ailsa Craig |
|
LA2529 |
Alcobaca |
|
LA2463 |
Allround |
|
LA1995 |
Angela |
|
LA3244 |
Antimold-B |
|
LA3527 |
Apex 1000 |
|
LA0657 |
Beaverlodge |
|
LA2973 |
Big Rainbow |
|
LA2972 |
Big Yellow Red Ctr. |
|
LA4347 |
B-L-35 |
|
LA1499 |
Break O'Day |
|
LA0198 |
Cal 255 |
|
LA2414 |
Cal Ace |
|
LA1439 |
Calmart |
|
LA3316 |
Campbell 24 |
|
LA3317 |
Campbell 28 |
|
LA3228 |
Canary Export |
|
LA2374 |
Caro Red |
|
LA2400 |
Castlemart |
|
LA3121 |
Chico Grande |
|
LA4285 |
CLN2264F |
|
LA4286 |
CLN2264G |
|
LA3213 |
Columbian |
|
LA0533 |
Condine Red |
|
LA0817 |
CP-2 |
|
LA3247 |
Craigella |
|
LA1162 |
Cuba Plum |
|
LA1219 |
Dwarf San Marzano |
|
LA0313 |
Dwarf Stone |
|
LA3245 |
E.S.1 |
|
LA4024 |
E-6203 |
|
LA3238 |
Earliana |
|
LA2006 |
Earlinorth |
|
LA0266 |
Earlipak |
|
LA3010 |
Earlipak |
|
LA0517 |
Early Santa Clara |
|
LA2711 |
Edkawi |
|
LA3800 |
Fargo Self-pruning |
|
LA3024 |
Fireball |
|
LA3840 |
FLA 7060 |
|
LA3242 |
Flora-Dade |
|
LA4026 |
Florida 7481 |
|
LA4025 |
Florida 7547 |
|
LA3030 |
Gardener |
|
LA2969 |
Georgia Streak |
|
LA2802 |
Globonnie |
|
LA4011 |
GT |
|
LA3231 |
Gulf State Market |
|
LA0314 |
Hardin Miniature |
|
LA3202 |
Hawaii 7997 |
|
LA3856 |
Hawaii 7998 |
|
LA4345 |
Heinz 1706-BG |
|
LA0806 |
High Crimson |
|
LA3237 |
Homestead 24 |
|
LA3320 |
Hotset |
|
LA3144 |
Hunt 100 |
|
LA2805 |
Indehiscent Currant |
|
LA3201 |
IRB 301 |
|
LA1089 |
John Baer |
|
LA1131 |
Kallio's Alaskan Dwarf |
|
LA0025 |
King Humbert #1 |
|
LA3240 |
Kokomo |
|
LA3526 |
L04012 |
|
LA0505 |
Laketa |
|
LA3203 |
Large Plum |
|
LA3118 |
Laurica |
|
LA0791 |
Long John |
|
LA0534 |
Lukullus |
|
LA3475 |
M-82 |
|
LA3120 |
Malintka 101 |
|
LA3007 |
Manapal |
|
LA2451 |
Manapal |
|
LA0502 |
Marglobe |
|
LA1504 |
Marmande |
|
LA0278 |
Marzano Grande |
|
LA3151 |
Mecline |
|
LA0011 |
Michigan State Forcing |
|
LA3911 |
Micro-Tom |
|
LA2825 |
Mobaci |
|
LA2824 |
Moboglan |
|
LA3152 |
Moboline |
|
LA2821 |
Mobox |
|
LA2830 |
Mocimor |
|
LA3471 |
Mogeor |
|
LA2828 |
Momor |
|
LA2829 |
Momor Verte |
|
LA2818 |
Monalbo |
|
LA2706 |
Moneymaker |
|
LA2819 |
Monita |
|
LA2713 |
Montfavet 167 |
|
LA2714 |
Montfavet 168 |
|
LA2827 |
Moperou |
|
LA2822 |
Mossol |
|
LA2820 |
Motabo |
|
LA2826 |
Motaci |
|
LA2823 |
Motelle |
|
LA3472 |
Movione |
|
LA2661 |
Nagcarlang |
|
LA3845 |
NC EBR-5 |
|
LA3846 |
NC EBR-6 |
|
LA3847 |
NC HS-1 |
|
LA3625 |
NC265-1 (93)-3-3 |
|
LA3802 |
New Hampshire Victor |
|
LA2009 |
New Yorker |
|
LA3321 |
Ohio 7663 |
|
LA1088 |
Ohio Globe A |
|
LA2447 |
Ontario 717 |
|
LA2449 |
Ontario 7517 |
|
LA2396 |
Ontario 7710 |
|
LA2448 |
Ontario 7818 |
|
LA2970 |
Orange, Red Ctr. |
|
LA2376 |
Pan American |
|
LA0012 |
Pearson |
|
LA0020 |
Pennheart |
|
LA3528 |
Peto 95-43 |
|
LA3243 |
Platense |
|
LA3312 |
Platense |
|
LA3125 |
Pomodorini Napolitan |
|
LA2715 |
Porphyre |
|
LA3820 |
Potentate |
|
LA3903 |
Primabel |
|
LA0089 |
Prince Borghese |
|
LA3233 |
Pritchard |
|
LA3229 |
Prospero |
|
LA2446 |
Purdue 135 |
|
LA2377 |
Purple Calabash |
|
LA2378 |
Purple Smudge |
|
LA0337 |
Red Cherry |
|
LA0276 |
Red Top VF |
|
LA3129 |
Rehovot 13 |
|
LA2356 |
Rey de Los Tempranos |
|
LA0535 |
Rheinlands Ruhm |
|
LA3343 |
Rio Grande |
|
LA3145 |
Rockingham |
|
LA0503 |
Roumanian Sweet |
|
LA3214 |
Rowpac |
|
LA2088 |
Royal Red Cherry |
|
LA3215 |
Roza |
|
LA1090 |
Rutgers |
|
LA2662 |
Saladette |
|
LA3216 |
Saladmaster |
|
LA3008 |
San Marzano |
|
LA0180 |
San Marzano (autodiploid) |
|
2-297 |
San Marzano (autodiploid) |
|
LA1021 |
Santa Cruz |
|
LA2413 |
Severianin |
|
LA2912 |
Short Red Cherry |
|
LA3234 |
Sioux |
|
LA3221 |
Slender Pear |
|
LA3632 |
Start 24 |
|
LA0030 |
Stemless Pennorange |
|
LA2443 |
Stirling Castle |
|
LA1091 |
Stokesdale |
|
LA1506 |
Stone |
|
LA0164 |
Sutton's Best of All |
|
LA2399 |
T-5 |
|
LA2590 |
T-9 |
|
LA0154 |
Tiny Tim |
|
LA1714 |
UC-134 |
|
LA3130 |
UC-204C |
|
LA1706 |
UC-82 |
|
LA2937 |
UC-MR20 |
|
LA2938 |
UC-N28 |
|
LA2939 |
UC-T338 |
|
LA2940 |
UC-TR44 |
|
LA2941 |
UC-TR51 |
|
LA0021 |
Uniform Globe |
|
LA2445 |
V-121 |
|
LA0745 |
V-9 Red Top |
|
LA3246 |
Vagabond |
|
LA3905 |
Vantage |
|
LA3122 |
Vendor |
|
LA2911 |
Vendor (Tm-2^a) |
|
LA2968 |
Vendor (Tm-2a) |
|
LA2971 |
Verna Orange |
|
LA2444 |
Vetomold K10 |
|
LA0744 |
VF-11 |
|
LA1023 |
VF-13L |
|
LA1507 |
VF-145 21-4 |
|
LA0816 |
VF-145 22-8 |
|
LA1222 |
VF145 78-79 |
|
LA0742 |
VF-34 |
|
LA0490 |
VF-36 |
|
LA0743 |
VF-6 |
|
LA2086 |
VFN Hi Sugar |
|
LA0815 |
VFN-14 |
|
LA1022 |
VFN-8 |
|
LA1221 |
VFNT Cherry |
|
LA3630 |
Vrbikanske nizke |
|
LA3465 |
Walter |
|
LA0279 |
Webb Special |
|
LA2464A |
White Beauty |
|
2-473 |
Yellow Cherry |
|
LA2804 |
Yellow Currant |
|
LA2357 |
Yellow Peach |
|
LA3148 |
Zemer Kau |
1.2. Latin American Cultivars (226)
This collection of Latin-American cultivars has been assembled from various sources but principally from our collecting trips, often at local markets. With a few exceptions they are indigenous in the sense that they are not recently introduced lines. Many of them are extinct in the source region, having been replaced by modern cultivars.
|
Accessions |
Location |
|
Bolivia |
|
|
LA0172 |
Santa Cruz |
|
LA2699 |
Coroica |
|
LA2871 |
Chamaca |
|
LA2873 |
Lote Pablo Luna #2 |
|
LA2874 |
Playa Ancha |
|
Brazil |
|
|
LA1021 |
Santa Cruz |
|
Chile |
|
|
LA0466 |
Hacienda Rosario |
|
LA0467 |
Lluta Valley |
|
LA0468 |
Iquique |
|
Colombia |
|
|
LA0356 - LA0358 |
Buenaventura |
|
LA1539 |
Cali to Popayan |
|
Costa Rica |
|
|
LA1215 |
|
|
LA3453A - LA3453D |
Turrialba |
|
Cuba |
|
|
LA1162 |
|
|
Ecuador |
|
|
LA0126 |
Quito mercado |
|
LA0292 |
Santa Cruz |
|
LA0408 - LA0410 |
Guayaquil |
|
LA0415 |
Daular |
|
LA0416 |
Puna |
|
LA0423 |
Wreck Bay: Cristobal |
|
LA1224 |
Puyo |
|
LA1238 |
Viche |
|
LA1239 - LA1241 |
Esmeraldas |
|
LA1244 |
Coop Carmela |
|
LA1249 |
Loja |
|
LA1250 |
Loja |
|
LA1251 |
Loja |
|
LA2094 |
El Naranjo |
|
LA2132 |
Chuchumbetza |
|
LA2381 - LA2384 |
Malacatos |
|
LA3126 |
Malacatos |
|
LA3624 |
Santa Rosa |
|
El Salvador |
|
|
LA1210 |
San Salvador |
|
LA1211 |
San Salvador |
|
Guatemala |
|
|
LA1460 |
Antigua |
|
Honduras |
|
|
LA0147 |
Tegucigalpa mercado |
|
LA0148 |
Tegucigalpa mercado |
|
Mexico |
|
|
LA0146 |
Mexico City mercado |
|
LA1218 |
Vera Cruz |
|
LA1459 |
Huachinango |
|
LA1462 |
Merida |
|
LA1544 |
Xol Laguna |
|
LA1564 |
Culiacan |
|
LA1565 |
Val. nacionale |
|
LA1566 |
Val. nacionale |
|
LA1567 |
Sinaloa |
|
LA1568 |
Yucatan |
|
LA1702 |
Sinaloa |
|
LA1703 |
Rio Tamesi |
|
LA1704 |
Rio Tamesi |
|
LA1994 |
|
|
LA2083 |
Guaco, Culiacan |
|
LA2084 |
Comala, Culiacan |
|
Nicaragua |
|
|
LA1212 |
|
|
LA1213 |
|
|
Panama |
|
|
LA1216 |
|
|
LA1217 |
|
|
Peru |
|
|
LA1570 |
Cerro Azul |
|
LA0113 |
Hacienda Calera |
|
LA0116 |
Chiclayo mercado |
|
LA0117 |
Piura mercado |
|
LA0125D |
Trujillo mercado |
|
LA0131H |
Arequipa mercado |
|
LA0134C |
Ayacucho mercado |
|
LA0393 - LA0396 |
Chiclayo |
|
LA0401 - LA0405 |
Piura |
|
LA0457 |
Tacna mercado |
|
LA0472 |
Tacna |
|
LA0473 |
Calana |
|
LA0477 |
Chincha |
|
LA0478 |
Chincha |
|
LA0721 |
Chiclayo |
|
LA1313 |
Convento de Sivia |
|
LA1315 |
Ayna |
|
LA1390 |
La Molina |
|
LA1397 |
Iquitos |
|
LA1398 |
Iquitos |
|
LA1650 |
Fundo Bogotalla |
|
LA1655 |
Tarapoto |
|
LA1669 |
Jahuay |
|
LA1698 |
Kradolfer Chacra |
|
LA1701 |
Trujillo |
|
LA1976A |
Calana |
|
LA1976B |
Calana |
|
LA1976C |
Calana |
|
LA1988 |
Iquitos |
|
LA2207 - LA2212 |
Bajo Naranjillo |
|
LA2213 - LA2220 |
Nueva Cajamarca |
|
LA2221 - LA2235 |
Moyobamba mercado |
|
LA2237 - LA2244 |
La Habana |
|
LA2245 - LA2253 |
Soritor |
|
LA2254 - LA2257 |
Puerto Moyobamba |
|
LA2258 |
Fundo Conovista |
|
LA2259A-2259D |
Moyobamba mercado |
|
LA2260 - LA2264 |
La Huarpia |
|
LA2265 - LA2268 |
Casaria de Pacaisapa |
|
LA2269 - LA2276 |
Km 57 from Tarapoto |
|
LA2278 - LA2282 |
Tabalosas |
|
LA2283 - LA2307 |
Tarapoto mercado |
|
LA2309 - LA2311 |
Punto Santa Cruz |
|
LA2316 |
Sargento |
|
LA2622 |
Mangual Pucallpa |
|
LA2623 |
Pucalepillo Pucallpa |
|
LA2676 |
San Juan del Oro |
|
LA2841 |
Chinuna |
|
LA2842 |
Santa Rita |
|
LA2843 |
Moyobamba mercado |
|
LA2844 |
Shanhao |
|
LA2845 |
Moyobamba mercado |
|
LA3222 - LA3226 |
San Isidro mercado |
|
LA3646 |
Puente Tincoj |
2. PREBRED STOCKS
2.1. Introgression Lines (ILs)
2.1.1. L. pennellii ILs (76)
The following group of introgression lines (ILs) was developed by Eshed & Zamir (Euphytica 79:175-179, 1994; TGC 49:26-30). Each IL (except IL8-1) is homozygous for a single introgression from L. pennellii (LA0716) in the background of L. esculentum cv. M-82 (LA3475). The entire L. pennellii genome is thereby represented by overlapping introgressions in a group of 50 lines. An additional 26 sublines provide increased mapping resolution in some regions. The IL # indicates the L. pennellii chromosome and introgressed segment number in each.
|
Access. |
Line |
|
LA4028 |
IL1-1 |
|
LA4029 |
IL1-1-2 |
|
LA4030 |
IL1-1-3 |
|
LA4031 |
IL1-2 |
|
LA4032 |
IL1-3 |
|
LA4033 |
IL1-4 |
|
LA4034 |
IL1-4-18 |
|
LA4035 |
IL2-1 |
|
LA4036 |
IL2-1-1 |
|
LAA4037 |
IL2-2 |
|
LA4038 |
IL2-3 |
|
LA4039 |
IL2-4 |
|
LA4040 |
IL2-5 |
|
LA4041 |
IL2-6 |
|
LA4042 |
IL2-6-5 |
|
LA4043 |
IL3-1 |
|
LA4044 |
IL3-2 |
|
LA3488 |
IL3-3 |
|
LA4046 |
IL3-4 |
|
LA4047 |
IL3-5 |
|
LA4048 |
IL4-1 |
|
LA4049 |
IL4-1-1 |
|
LA4050 |
IL4-2 |
|
LA4051 |
IL4-3 |
|
LA4052 |
IL4-3-2 |
|
LA4053 |
IL4-4 |
|
LA4054 |
IL5-1 |
|
LA4055 |
IL5-2 |
|
LA4056 |
IL5-3 |
|
LA4057 |
IL5-4 |
|
LA4058 |
IL5-5 |
|
LA4059 |
IL6-1 |
|
LA4060 |
IL6-2 |
|
LA4061 |
IL6-2-2 |
|
LA4062 |
IL6-3 |
|
LA4063 |
IL6-4 |
|
LA4064 |
IL7-1 |
|
LA4065 |
IL7-2 |
|
LA4066 |
IL7-3 |
|
LA4067 |
IL7-4 |
|
LA4068 |
IL7-4-1 |
|
LA4069 |
IL7-5 |
|
LA4070 |
IL7-5-5 |
|
LA4071 |
IL8-1 |
|
LA4072 |
IL8-1-1 |
|
LA4073 |
IL8-1-5 |
|
LA4074 |
IL8-2 |
|
LA4075 |
IL8-2-1 |
|
LA4076 |
IL8-3 |
|
LA4077 |
IL8-3-1 |
|
LA4078 |
IL9-1 |
|
LA4079 |
IL9-1-2 |
|
LA4080 |
IL9-1-3 |
|
LA4081 |
IL9-2 |
|
LA4082 |
IL9-2-5 |
|
LA4083 |
IL9-2-6 |
|
LA4084 |
IL9-3 |
|
LA4085 |
IL9-3-1 |
|
LA4086 |
IL9-3-2 |
|
LA4087 |
IL10-1 |
|
LA4088 |
IL10-1-1 |
|
LA4089 |
IL10-2 |
|
LA4090 |
IL10-2-2 |
|
LA4091 |
IL10-3 |
|
LA4092 |
IL11-1 |
|
LA4093 |
IL11-2 |
|
LA4094 |
IL11-3 |
|
LA4095 |
IL11-4 |
|
LA4096 |
IL11-4-1 |
|
LA4097 |
IL12-1 |
|
LA4098 |
IL12-1-1 |
|
LA4099 |
IL12-2 |
|
LA4100 |
IL12-3 |
|
LA4101 |
IL12-3-1 |
|
LA4102 |
IL12-4 |
|
LA4103 |
IL12-4-1 |
2.1.2. L. hirsutum ILs (98)
The following group of introgression lines represent the genome of L. hirsutum (LA1777) in the background of L. esculentum cv. E-6203 (LA4024) via homozygous chromosome segments (Monforte & Tanksley, Genome 43:803-813; 2000). The first 57 lines (LA3913 - LA3969) represent approximately 85% of the donor genome, while the remaining 41 lines (LA3970 - LA4010) contain different introgressions, mostly derivatives of the first group. Unlike the L. pennellii ILs above, each L. hirsutum line may contain more than one introgression, representing one to several chromosomes, as indicated below.
|
Access. |
Line |
Chr. |
|
LA3913 |
TA1258 |
1 |
|
LA3914 |
TA523 |
1 |
|
LA3915 |
TA1229 |
1 |
|
LA3916 |
TA1223 |
1 |
|
LA3917 |
TA1535 |
1 |
|
LA3918 |
TA1127 |
1 |
|
LA3919 |
TA1128 |
1 |
|
LA3920 |
TA1536 |
1 |
|
LA3921 |
TA1105 |
2 |
|
LA3922 |
TA1266 |
2 |
|
LA3923 |
TA1537 |
2 |
|
LA3924 |
TA1538 |
2 |
|
LA3925 |
TA1111 |
3 |
|
LA3926 |
TA1276 |
3 |
|
LA3927 |
TA1277 |
3 |
|
LA3928 |
TA1540 |
3 |
|
LA3929 |
TA1541 |
3 |
|
LA3930 |
TA1133 |
4 |
|
LA3931 |
TA1280 |
4 |
|
LA3932 |
TA1562 |
4 |
|
LA3933 |
TA1542 |
4 |
|
LA3934 |
TA1459 |
4 |
|
LA3935 |
TA517 |
4 |
|
LA3936 |
TA1475 |
4 |
|
LA3937 |
TA1473 |
4 |
|
LA3938 |
TA1287 |
5 |
|
LA3939 |
TA1293 |
5 |
|
LA3940 |
TA1112 |
5 |
|
LA3941 |
TA1543 |
5 |
|
LA3942 |
TA1117 |
5 |
|
LA3943 |
TA1544 |
5 |
|
LA3944 |
TA1539 |
6 |
|
LA3945 |
TA1545 |
6 |
|
LA3946 |
TA1546 |
6 |
|
LA3947 |
TA1559 |
6 |
|
LA3948 |
TA1303 |
7 |
|
LA3949 |
TA1304 |
7 |
|
LA3950 |
TA1547 |
7 |
|
LA3951 |
TA1312 |
7 |
|
LA3952 |
TA1315 |
8 |
|
LA3953 |
TA1316 |
8 |
|
LA3954 |
TA1548 |
8 |
|
LA3955 |
TA1320 |
8 |
|
LA3956 |
TA1324 |
9 |
|
LA3957 |
TA1325 |
9 |
|
LA3958 |
TA1330 |
9 |
|
LA3959 |
TA1331 |
9 |
|
LA3960 |
TA1550 |
10 |
|
LA3961 |
TA1551 |
10 |
|
LA3962 |
TA1552 |
10 |
|
LA3963 |
TA1337 |
10 |
|
LA3964 |
TA1339 |
10 |
|
LA3965 |
TA1555 |
11 |
|
LA3966 |
TA1554 |
11 |
|
LA3967 |
TA1342 |
11 |
|
LA3968 |
TA1350 |
12 |
|
LA3969 |
TA1121 |
12 |
|
LA3970 |
TA1219 |
1 |
|
LA3971 |
TA1218 |
2 |
|
LA3972 |
TA1173 |
2 |
|
LA3975 |
TA1629 |
3 |
|
LA3976 |
TA1138 |
4 |
|
LA3977 |
TA1467 |
4 |
|
LA3978 |
TA1468 |
4 |
|
LA3979 |
TA1630 |
4 |
|
LA3980 |
TA1290 |
5 |
|
LA3981 |
TA1116 |
5 |
|
LA3983 |
TA1631 |
5 |
|
LA3984 |
TA1632 |
5 |
|
LA3985 |
TA1306 |
7 |
|
LA3986 |
TA1309 |
7 |
|
LA3988 |
TA1318 |
8 |
|
LA3989 |
TA1319 |
8 |
|
LA3990 |
TA1560 |
8 |
|
LA3991 |
TA1326 |
9 |
|
LA3993 |
TA1549 |
10 |
|
LA3994 |
TA1635 |
10 |
|
LA3995 |
TA1553 |
11 |
|
LA3996 |
TA1120 |
11 |
|
LA3997 |
TA1563 |
1, 10 |
|
LA3998 |
TA1637 |
1, 11, 12 |
|
LA3999 |
TA1638 |
1, 12 |
|
LA4000 |
TA1557 |
1, 4 |
|
LA4001 |
TA1644 |
1, 7, 12 |
|
LA4002 |
TA1645 |
1, 8, 12 |
|
LA4003 |
TA1648 |
2, 11 |
|
LA4004 |
TA1649 |
2, 3, 6 |
|
LA4005 |
TA1652 |
3, 5 |
|
LA4006 |
TA1654 |
4, 10, 11 |
|
LA4007 |
TA1655 |
4, 12 |
|
LA4008 |
TA1656 |
5, 6, 9 |
|
LA4009 |
TA1564 |
5, 7, 10 |
|
LA4010 |
TA1561 |
8, 12 |
2.1.3. S. lycopersicoides IL (99)
The following group of ILs have been bred from S. lycopersicoides into the background of L. esculentum cv. VF36. These lines represent ~96% of the donor genome and are described in the following publications: Canady et al., 2005, Genome 48: 685-697; Rick et al. 1988 Theor. Appl. Genet. 76: 647-655. While some lines are available in the homozygous condition, many others are associated with sterility and must be maintained via heterozygotes. Marker analysis is required to identify heterozygous progeny. Seed of some lines may be limited or temporarily unavailable.
|
Acc. |
Line |
Chr.s |
|
LA3344 |
Mdh-1 |
3 |
|
LA3345 |
Dia-3 |
9 |
|
LA3668 |
Abg |
10 |
|
LA3866 |
LS1-1 |
1 |
|
LA3867 |
LS11-9 |
1 |
|
LA3869 |
LS42-4 |
2 |
|
LA3870 |
LS38-10 |
2 |
|
LA3871 |
LS41-3 |
2 |
|
LA3874 |
LS20-9 |
3 |
|
LA3875 |
LS24-14 |
4, 12 |
|
LA3876 |
LS29-1 |
8 |
|
LA3878 |
LS24-6 |
5 |
|
LA3879 |
LS1-5 |
5, 11 |
|
LA3882 |
LS43-14 |
2, 6 |
|
LA3883 |
LS48-6 |
7, 11 |
|
LA3886 |
LS48-5 |
7 |
|
LA3889 |
LS41-13 |
8 |
|
LA3892 |
LS48-2 |
11 |
|
LA3893 |
LS16-6 |
5, 12 |
|
LA3906 |
Wa , Dl |
8 |
|
LA4230 |
LS15-2H |
1 |
|
LA4231 |
LS15-2B |
1 |
|
LA4232 |
LS11-11A |
1 |
|
LA4233 |
LS20-9 |
1 |
|
LA4234 |
LS21-2 |
1 |
|
LA4235 |
LS10-2 |
1 |
|
LA4236 |
LS49-8A |
2 |
|
LA4237 |
LS40-8 |
2 |
|
LA4238 |
LS5-1 |
2 |
|
LA4239 |
LS41-20 |
2 |
|
LA4240 |
LS1-13 |
3 |
|
LA4241 |
LS40-2 |
3 |
|
LA4242 |
LS14-8 |
3 |
|
LA4243 |
LS1-3 |
3 |
|
LA4244 |
LS10-9 |
4 |
|
LA4245 |
LS10-11A |
4 |
|
LA4246 |
LS49-8B |
4 |
|
LA4247 |
LS12-9 |
4 |
|
LA4248 |
LS11-6 |
5 |
|
LA4249 |
LS9-1 |
5 |
|
LA4250 |
LS49-8C |
5 |
|
LA4251 |
LS49-3 |
5 |
|
LA4252 |
LS32-11 |
5 |
|
LA4253 |
LS11-11B |
6 |
|
LA4254 |
LS32-14 |
6 |
|
LA4255 |
LS38-5 |
6 |
|
LA4256 |
LS9-22 |
6 |
|
LA4257 |
LS46-3 |
7 |
|
LA4258 |
LS19-7 |
7 |
|
LA4259 |
LS32-4 |
7 |
|
LA4260 |
SL-7F |
7 |
|
LA4261 |
LS8-11 |
7 |
|
LA4262 |
LS20-16 |
8 |
|
LA4263 |
LS46-6A |
8 |
|
LA4264 |
LS9-26A |
8 |
|
LA4265 |
LS9-26B |
8 |
|
LA4266 |
SL-8A |
8 |
|
LA4267 |
LS16-10 |
8 |
|
LA4268 |
LS14-7 |
9 |
|
LA4269 |
LS12-2 |
9 |
|
LA4270 |
LS10-6 |
9 |
|
LA4271 |
LS49-5 |
9 |
|
LA4272 |
LS41-11 |
9 |
|
LA4273 |
LS12-8 |
10 |
|
LA4274 |
LS4-14 |
10 |
|
LA4275 |
SL-10 |
10 |
|
LA4276 |
LS12-12 |
10 |
|
LA4277 |
LS24-11 |
11 |
|
LA4278 |
LS3-2 |
11 |
|
LA4279 |
LS19-11 |
11 |
|
LA4280 |
LS1-5 |
11, 5 |
|
LA4281 |
LS13-13 |
12 |
|
LA4282 |
LS45-7 |
12 |
|
LA4283 |
LS8-9 |
12 |
|
LA4284 |
LS9-13 |
12 |
|
LA4293 |
LS5-8 |
1 |
|
LA4294 |
LS15-2AD |
1 |
|
LA4295 |
LS15-2A |
1 |
|
LA4296 |
LS15-2AA |
1 |
|
LA4297 |
LS15-2AAA |
1 |
|
LA4298 |
LS15-2BA |
1 |
|
LA4299 |
LS4-9 |
5 |
|
LA4300 |
LS9-7B |
5, 6 |
|
LA4301 |
SL-7A |
7 |
|
LA4302 |
SL-7C |
7 |
|
LA4303 |
SL-7D |
7 |
|
LA4304 |
LS8-11A |
7 |
|
LA4305 |
LS9-26C |
7, 8 |
|
LA4306 |
LS46-6 |
8 |
|
LA4307 |
SL-8 |
8 |
|
LA4308 |
LS32-10 |
9 |
|
LA4309 |
LS10-6D |
9 |
|
LA4310 |
LS19-10A |
11 |
|
LA4311 |
LS14-2 |
12 |
|
LA4312 |
LS45-7C |
12 |
|
LA4313 |
LS8-12A |
12 |
|
LA4314 |
LS12-9B |
4, 10 |
|
LA4315 |
SL-7 |
7 |
2.2. Backcross Recombinant Inbreds (99).
The following group of backcross recombinant inbred lines originated from the cross L. esculentum × L. pimpinellifolium (Doganlar et al. Genome 45: 1189-1202, 2002). The result of 2 BC’s and at least 6 generations of inbreeding via single seed descent, the lines are highly homozygous (residual heterozygosity ~3%). The population has been genotyped at 127 marker loci, and the corresponding maps, map files, and QTL data are available from the Solanaceae Genome Network (www.sgn.cornell.edu). This set of 99 lines has been selected for optimum mapping resolution using the MapPop software, and provide a permanent, high resolution mapping population.
LA4139 through LA4229 BC-RIs
LA4024 L. esculentum parent (E-6203)
LA1589 L. pimpinellifolium parent
2.3. Alien Substitution Lines (7)
In the course of his study of segregation and recombination in L. esculentum x L. pennellii hybrids, Rick (Genetics 26:753-768, 1969; Biol. Zbl. 91:209-220, 1971) progressively backcrossed certain chromosomes of L. pennellii LA0716 into L. esculentum. Selected heterozygotes of later generations were selfed and subsequent progenies free of esculentum markers were selected as the substitution lines. The chromosome 6 substitution (LA3142) was further selected with RFLP markers to eliminate residual heterozygosity (Weide et al., Genetics 135:1175-1186, 1993). The mutant loci used to select each substitution are indicated.
|
LA |
Chrom. |
Marker Loci |
|
2091 |
1 |
au, dgt, inv, scf |
|
1639 |
2 |
Me, aw, m, d |
|
1640 |
3 |
sy, bls, sf |
|
3469 |
4 |
clau, ful, ra, e, su3 |
|
3142 |
6 |
yv, ndw, m-2, c |
|
1642 |
8 |
l, bu, dl, al |
|
1643 |
11 |
j, hl, a |
2.4. Monosomic Alien Addition Lines (10)
In the following group of monosomic additions (MA), each line contains a single extra chromosome from S. lycopersicoides LA1964 added to the L. esculentum genome (Chetelat et al., Genome 41:40-50, 1998). Intactness of the S. lycopersicoides chromosomes in these stocks has been tested with a limited number of markers, hence some may be recombinant. For example, our stock of MA-8 lacks S. lycopersicoides markers distal to TG330 on the long arm. Furthermore, we were unable to maintain MA-1 and MA-6, both of which are now extinct.
Like other types of trisomics, progeny of the monosomic additions include both diploids and trisomics, the proportion of which varies between each chromosome group. Identification of monosomic additions in each generation is facilitated by their phenotypic resemblance to the corresponding primary trisomic. Therefore, the guidelines of Rick (TGC 37:60-61, 1987) for identifying trisomics in the seedling stage are useful for selecting monosomic additions as well. To further simplify this process, we have backcrossed some of the monosomic additions into the background of multiple marker stocks for the corresponding chromosomes. In this configuration, diploids are more easily distinguished from trisomics by the expression of recessive mutant alleles in the former, and dominant wild type in the latter. For example, in our stock of MA-2, the 2n progeny would have the phenotype wv-aa-d, whereas 2n+1 plants would be wild type at these marker loci (as well showing the expected trisomic syndrome). In addition, some monosomic additions carry dominant morphological markers that can be used to distinguish them from 2n progeny. The marker genotypes of 2n+1 vs 2n progeny are listed below for each chromosome.
|
LA |
Chrom. |
2n+1 |
2n |
|
3454 |
MA-2 |
+-+-+ |
wv-aa-d |
|
3455 |
MA-3 |
+-+-+ |
sy-bls-sf |
|
3456 |
MA-4 |
+ |
+ |
|
3457 |
MA-5 |
+ |
obv |
|
3459 |
MA-7 |
Bco-+-+ |
+-var-not |
|
3460 |
MA-8 |
Wa |
+ |
|
3461 |
MA-9 |
+ |
+ |
|
3462 |
MA-10 |
Abg-+-+-+-+ |
+-u-t-nd-ag |
|
3463 |
MA-11 |
+ |
+ |
|
3464 |
MA-12 |
+ |
+ |
2.5. Other Prebreds (13). This group of prebreds contain selected morphological traits bred into cultivated tomato from related wild species. Some traits may be simply inherited, others likely involve multiple genetic loci. Also included are two interspecific hybrids useful for various purposes.
2.5.1. High soluble solids derivatives of L chmielewskii. Bred from LA1028 into the background of VF145-7879 (Rick, 1974, Hilgardia 42:493-510).
LA1500
LA1501
LA1502
LA1503
LA1563.
2.5.2. Monogenic and provisional mutants from L. cheesmanii (Rick, Econ. Bot. 21: 171-184, 1967).
LA1015 h, ‘cps’ (compressed fruit = reduced L/W ratio)
LA1016 dps, ‘yg’ (yellow green leaves)
LA1017 ptb, ‘Ppc’ (pachypericarp = thick-walled fruit)
LA1018 ptb, uG, Od, h, dark buds (anthocyanin in bud calyces), bitter fruit
LA1019 ‘Ppc’, thick calyx, firm fruit
2.5.3. Exserted stigmas from L. pimpinellifolium. Bred from LA1585 (Rick TGC 33:13-14, 1983):
LA2380
2.5.4. Interspecific hybrids.
LA3857 L. esculentum cv. VF36 × S. lycopersicoides LA2951, relatively male-fertile F1 hybrid (clonally propagated).
LA4135 L. esculentum cv. VF36 × L. pennellii LA0716; useful as a rootstock for maintenance of S. sitiens,
3. STRESS TOLERANT STOCKS (50+)
We receive many requests for stocks with tolerances to environmental stresses (abiotic or biotic). Therefore, we chose this group of mostly wild species accessions based on our observations of plants in their native habitats and/or reports in the literature. If TGC members know of other accessions which should be added to this group, we would be grateful for the information and seed samples to accession in the TGRC.
3.1. Drought tolerance
L. pennellii (general feature): LA0716, and others
L. chilense (esp. coastal sites): LA1958, LA1959, LA1972, and others
S. sitiens (general feature): LA1974, LA2876, LA4105, and others
3.2. Flooding tolerance
L. esculentum var. cerasiforme (wet tropics): LA1421, and others
S. juglandifolium, S. ochranthum (probably a general feature): LA2120, LA2682
3.3. High temperature tolerance
L. esculentum cv.s Nagcarlang (LA2661), Saladette (LA2662), Malintka-101 (LA3120), Hotset (LA3320)
3.4. Chilling tolerance
L. hirsutum (from high altitudes): LA1363, LA1393, LA1777, LA1778
L. chilense (from high altitudes): LA1969, LA1971, LA4117A
S. lycopersicoides (from high altitudes): LA1964, LA2408, LA2781
3.5. Aluminum tolerance
L. esculentum var. cerasiforme LA2710 (suspected)
3.6. Salinity and/or alkalinity tolerance
L. cheesmanii (from littoral habitats): LA1401, LA1508, LA3124, LA3909
L. chilense: LA1930, LA1932, LA1958, LA2747, LA2748, LA2880, LA2931
L. esculentum cv. Edkawi LA2711
L. esculentum var. cerasiforme: LA1310, LA2079 - LA2081, LA4133
L. pennellii: LA0716, LA1809, LA1926, LA1940, LA2656
L. peruvianum: LA0462, LA1278, LA2744
L. pimpinellifolium LA1579
3.7. Arthropod resistance
L. hirsutum, esp. f. glabratum: LA0407 and many others
L. pennellii: LA0716, and others
4. CYTOGENETIC STOCKS
4.1. Translocations (37)
The following group of translocation stocks have been assembled from the collections of their originators - D.W. Barton, C.D. Clayberg, B.S. Gill, G.R. Stringham, B. Snoad, and G. Khush. As far as we know, they are all homozygous for the indicated structural changes. They are described by Gill et al. (TGC 23: 17-18; TGC 24:10-12). Accessions with an asterisk comprise the tester set.
|
Accession |
Chrom.s |
|
*LA1115 |
T9-12 |
|
*LA1119 |
T3-8 |
|
*LA1120 |
T6-12 |
|
*LA1876 |
T1-2* |
|
*LA1885 |
T5-7* |
|
*LA1898 |
T2-10a* |
|
*LA1899 |
T6-11* |
|
*LA1903 |
T4-7* |
|
LA1049 |
T1-9 |
|
LA1116 |
T1-11 |
|
LA1117 |
T5-7 |
|
LA1118 |
T7-11 |
|
LA1121 |
T4-9 |
|
LA1122 |
T2-9 |
|
LA1123 |
T2-9 |
|
LA1124 |
T3-9 |
|
LA1125 |
T5-7 |
|
LA1126 |
T7-9 |
|
LA1127 |
T3-5 |
|
LA1129 |
T3-9 |
|
LA1877 |
T2-4 |
|
LA1878 |
T2-7 |
|
LA1879 |
T2-9 |
|
LA1880 |
T2-11 |
|
LA1881 |
T2-12 |
|
LA1882 |
T12-3 or -8 |
|
LA1883 |
T3-7 |
|
LA1884 |
2 IV T3-8,9-12 |
|
LA1886 |
T12-3 or 8 |
|
LA1892 |
2 IV T9-12, ?-? |
|
LA1894 |
T2-9a |
|
LA1895 |
T2-9b |
|
LA1896 |
T1-12 |
|
LA1897 |
T7-11? |
|
LA1902 |
T2- ? |
|
LA1904 |
T2-9d |
|
LA1905 |
T1-3 or 8 |
|
LA1906 |
T2-10b |
4.2. Trisomics (35)
The following series of trisomics contain various kinds of extra chromosomes. Since the extras are transmitted irregularly, each stock necessarily produce a majority of diploid progeny, the remainder aneuploid. Primary trisomics yield mostly 2n and 2n+1, and rarely tetrasomics (2n+2). Telotrisomics yield telos and an occasional rare tetratelosomic. Secondary, tertiary, and compensating trisomics transmit other trisomic types as expected. Because transmission is irregular and reproduction of stocks requires much labor, our stocks are limited. In requesting our aneuploids, researchers are asked to keep these points in mind. To assist in the identification of primary trisomics at the seedling stage, the key features of each have been summarized by Rick (TGC 37:60-61, 1987). Additional 2n+1 stocks are listed under Monosomic Alien Additions.
|
Accession |
Genotype |
|
|
Primary trisomics |
||
|
delta-10 |
Triplo-1 |
|
|
delta-06 |
Triplo-2 |
|
|
delta-08 |
Triplo-3 |
|
|
delta-02 |
Triplo-4 |
|
|
delta-04 |
Triplo-5 |
|
|
delta-12 |
Triplo-6 |
|
|
delta-07 |
Triplo-7 |
|
|
delta-03 |
Triplo-8 |
|
|
delta-05 |
Triplo-9 |
|
|
delta-01 |
Triplo-10 |
|
|
delta-40 |
Triplo-11 |
|
|
delta-09 |
Triplo-12 |
|
|
Telo-trisomics |
||
|
delta-14 |
2n + 3S |
|
|
delta-17 |
2n + 3L |
|
|
delta-21 |
2n + 4L |
|
|
delta-20 |
2n + 7L |
|
|
delta-19 |
2n + 8L |
|
|
delta-35 |
2n + 10S |
|
|
Secondary trisomics |
||
|
delta-44 |
2n + 2S.2S |
|
|
delta-43 |
2n + 5L.5L |
|
|
delta-36 |
2n + 7S.7S |
|
|
delta-26 |
2n + 9S.9S |
|
|
delta-31 |
2n + 9L.9L |
|
|
delta-28 |
2n + 10L.10L |
|
|
delta-41 |
2n + 11L.11L |
|
|
delta-29 |
2n + 12L.12L |
|
|
Tertiary trisomics |
||
|
delta-18 |
2n + 2L.10L |
|
|
delta-16 |
2n + 4L.10L |
|
|
delta-39 |
2n + 5L.7S |
|
|
delta-15 |
2n + 7S.11L |
|
|
delta-25 |
2n + 9L.12L |
|
|
delta-23 |
2n + 1L.11L |
|
|
Compensating trisomics |
||
|
delta-32 |
2n - 3S.3L + 3S + 3L.3L |
|
|
delta-33 |
2n - 3S.3L + 3S.3S + 3L.3L |
|
|
delta-34 |
2n - 7S.7L + 7S.7S + 7L.7L |
|
4.3. Autotetraploids (17)
We are currently maintaining only the following group of tetraploids. Whereas we formerly stocked many more lines, their rapid deterioration, low seed yields, and lack of demand required that we prune them to a smaller group of more frequently used genotypes. All are L. esculentum unless otherwise noted, and arose from either induced or spontaneous chromosome doubling.
|
Accession |
Genotype |
|
2-095 |
cv. San Marzano |
|
2-483 |
cv. Red Cherry |
|
LA0457 |
cv. from Tacna mercado |
|
LA0794 |
ag, tv |
|
LA1917 |
L. chilense |
|
LA2335 |
L. pimpinellifolium |
|
LA2337 |
cv. Stokesdale |
|
LA2339 |
cv. Pearson |
|
LA2340 |
L. pimpinellifolium |
|
LA2342 |
cv. Danmark |
|
LA2343 |
cv. Waltham Fog |
|
LA2581 |
L. peruvianum |
|
LA2582 |
L. peruvianum var. humifusum |
|
LA2583 |
L. chilense |
|
LA2585 |
L. pimpinellifolium |
|
LA2587 |
L. esculentum var. cerasiforme |
|
LA3255 |
cv. Ailsa Craig |
5. CYTOPLASMIC VARIANTS (3)
The following three lines are cytoplasmically-inherited chlorotic variants maintained by the TGRC and included in the miscellaneous group for want of better classification. They were induced by mutagens and are inherited in strictly maternal fashion. They are not transmitted by pollen but in reciprocal crosses -- no matter what male parents we have used -- the progeny are 100% variant.
LA1092 Uniform yellow, induced by fast neutrons in hybrid background (G.S. Khush)
LA1438 Light green, induced by X-rays in cv. Moneymaker (K. Kerkerk)
LA2979 Cyto-variegated, in cv. Glamour (R.W. Robinson)
6. GENETIC MARKER COMBINATIONS
6.1. Chromosome Marker Stocks (182)
This group consists of stocks in each of which has been assembled a series of marker genes for a single chromosome. In a few cases markers on other chromosomes are also present (listed in parentheses). Some of the more useful stocks have been combined with male steriles in order to make them useful for large scale test crossing. These stocks are listed below according to chromosome, and within each chromosome group by accession number. Asterisks indicate the preferred marker combination for each chromosome (i.e. that which provides the best map coverage).
|
Access. |
Genotype |
||||
|
Chromosome 1 |
|||||
|
LA0910 |
per, inv |
||||
|
LA0984 |
scf, inv |
||||
|
LA0985 |
inv, per |
||||
|
LA1003 |
scf, inv, per |
||||
|
LA1082 |
era, um |
||||
|
LA1107 |
inv, co |
||||
|
LA1108 |
inv, dgt |
||||
|
LA1169 |
scf, dgt |
||||
|
LA1173 |
gas, co |
||||
|
LA1184 |
autl, dgt |
||||
|
LA1185 |
autl, scf, inv |
||||
|
LA1186 |
autl, scf, inv, dgt |
||||
|
LA1431 |
autl, dgt |
||||
|
LA1490 |
autl, co, inv, dgt |
||||
|
LA1492 |
ms-32, bs |
||||
|
LA1529* |
autl, co, scf, inv, dgt |
||||
|
LA2354 |
br, y (p, l) |
||||
|
LA3209 |
imb, irr, y |
||||
|
LA3301 |
fla, comin |
||||
|
LA3302 |
imb, comin |
||||
|
LA3303 |
imb, inv |
||||
|
LA3305 |
imb, Lpg |
||||
|
LA3306 |
comin, inv |
||||
|
LA3307 |
comin, Lpg |
||||
|
LA3346 |
au, bs |
||||
|
LA3347 |
au, ms-32 |
||||
|
LA3348 |
au, com |
||||
|
LA3349 |
au, imb |
||||
|
LA3350 |
au, br |
||||
|
LA3351 |
imb, Lpg/+ |
||||
|
LA3352 |
imb, au, Lpg/+ ? |
||||
|
Chromosome 2 |
|||||
|
LA0271 |
aw, O |
||||
|
LA0286 |
d, m |
||||
|
LA0310 |
Wom, d |
||||
|
LA0330 |
bk, o, p, d, s (r, y) |
||||
|
LA0342 |
Wom, d (ms-17) |
||||
|
LA0514 |
aw, Wom, d |
||||
|
LA0639 |
Me, aw, d |
||||
|
LA0650 |
aw, d |
||||
|
LA0715 |
Wom, Me, aw, d |
||||
|
LA0732 |
suf, d |
||||
|
LA0733 |
Wom, d, ms-10 |
||||
|
LA0754 |
aw, p, d, m, o |
||||
|
LA0777 |
dil, d |
||||
|
LA0789 |
Me, aw, d, m |
||||
|
LA0790 |
wv, Me, aw, d |
||||
|
LA0986 |
s, bk, Wom, o, aw, p, d |
||||
|
LA1525 |
aa, d |
||||
|
LA1526 |
are, wv, d |
||||
|
LA1699 |
Wom, bip |
||||
|
LA1700* |
wv, aa, d |
||||
|
LA3132 |
Prx-21, ms-10, aa |
||||
|
Chromosome 3 |
|||||
|
LA0644 |
r, wf |
||||
|
LA0782 |
sy, sf |
||||
|
LA0877 |
pau, r |
||||
|
LA0880 |
sf, div |
||||
|
LA0987 |
pli, con |
||||
|
LA0988 |
ru, sf |
||||
|
LA1070 |
ru, sf, cur |
||||
|
LA1071 |
sy, bls, sf |
||||
|
LA1101 |
cn, sy, sf |
||||
|
LA1175 |
bls, aut |
||||
|
LA1430* |
sy, Ln, bls, sf |
||||
|
Chromosome 4 |
|||||
|
LA0774 |
ful, e |
||||
|
LA0885 |
ful, e, su3 |
||||
|
LA0886 |
ful, ra, e |
||||
|
LA0888 |
ful, ven, e |
||||
|
LA0889 |
ra, su3 |
||||
|
LA0890 |
ra, ven |
||||
|
LA0902 |
ful, ra2, e (ms-31) |
||||
|
LA0915 |
clau, ful |
||||
|
LA0916 |
clau, ra, su3 |
||||
|
LA0917* |
clau, ful, ra, e, su3 |
||||
|
LA0920 |
ful, ra, e, su3 |
||||
|
LA0989 |
afl, ful |
||||
|
LA0990 |
cm, ful, e, su3 |
||||
|
LA0992 |
clau, ra, su3 (com) |
||||
|
LA0993 |
ra, si |
||||
|
LA0994 |
cm, ver |
||||
|
LA1073 |
clau, afl |
||||
|
LA1074 |
clau, ver |
||||
|
LA1075 |
ver, e, su3 |
||||
|
LA1536 |
clau, su3, ra; icn |
||||
|
Chromosome 5 |
|||||
|
LA0512 |
mc, tf, wt, obv |
||||
|
LA1188 |
frg, tf |
||||
|
LA3850* |
af, tf, obv |
||||
|
Chromosome 6 |
|||||
|
LA0336 |
c, sp (a, y) |
||||
|
LA0640 |
yv, c |
||||
|
LA0651 |
m-2, c |
||||
|
LA0773 |
yv, m-2, c |
||||
|
LA0802 |
yv, m-2, c (ms-2) |
||||
|
LA0879 |
tl, yv |
||||
|
LA1178 |
yv, coa, c |
||||
|
LA1189* |
pds, c |
||||
|
LA1190 |
pds, yv |
||||
|
LA1489 |
yv, ves-2, c |
||||
|
LA1527 |
d-2, c |
||||
|
LA3805 |
m-2, gib-1 |
||||
|
LA3806 |
yv, Mi, Bog, sp, c |
||||
|
LA3807 |
tl, yv, c |
||||
|
Chromosome 7 |
|||||
|
LA0788 |
La/+, deb |
||||
|
LA0882 |
La/+, deb, adp |
||||
|
LA0923 |
ig, La/+ |
||||
|
LA0924 |
La/+, not |
||||
|
LA1083 |
ig, flc |
||||
|
LA1103* |
var, not |
||||
|
LA1104 |
deb, not |
||||
|
LA1172 |
La/+, lg-5 |
||||
|
Chromosome 8 |
|||||
|
LA0513 |
l, bu, dl |
||||
|
LA0712 |
l, bu, dl; ms-2 |
||||
|
LA0776 |
l, vavirg |
||||
|
LA0897 |
l, bu, dl, al |
||||
|
LA0922 |
bu, dl, spa |
||||
|
LA0998 |
l, bu, dl, Pn/+ |
||||
|
LA0999 |
tp, dl |
||||
|
LA1012 |
dl, l |
||||
|
LA1191 |
spa, ae |
||||
|
LA1442 |
dl, glg, marm |
||||
|
LA1666* |
l, bu, dl, ae |
||||
|
Chromosome 9 |
|||||
|
LA0883 |
pum, ah |
||||
|
LA0884 |
wd, marm |
||||
|
LA1000 |
nv, ah |
||||
|
LA1001 |
pum, ah, marm |
||||
|
LA1100 |
ah, pla, marm |
||||
|
LA1112 |
marm, lut |
||||
|
LA1176 |
Crk, ah, marm |
||||
|
LA3353* |
ah, marm, pct |
||||
|
LA3841 |
Tm-2a, Frl, nv, ™ |
||||
|
Chromosome 10 |
|||||
|
LA0158 |
Xa/+, u, t (y) |
||||
|
LA0339 |
ag, u |
||||
|
LA0341 |
h, ag (ms-2) |
||||
|
LA0643 |
u, l-2 |
||||
|
LA0649 |
tv, ag |
||||
|
LA0711 |
tv, ag (ms-2) |
||||
|
LA1002 |
h, u, l-2, t, ag (pe, lg) |
||||
|
LA1085 |
h, res |
||||
|
LA1086 |
h, ten |
||||
|
LA1110 |
icn, ag |
||||
|
LA1192 |
hy, ag |
||||
|
LA1487 |
icn, tv |
||||
|
LA2493 |
Xa-2, hy, h, ag |
||||
|
LA2495 |
Xa-2, h, ten, ag, al |
||||
|
LA2496 |
Xa-2, h, l-2, t |
||||
|
LA2497 |
hy, u, icn, h, ag |
||||
|
LA2498 |
u, Xa-3, h |
||||
|
LA2499 |
u, nor, t |
||||
|
LA2500 |
u, icn, h |
||||
|
LA2501 |
u, icn, h, ag |
||||
|
LA2502 |
u, h, auv, l-2, tv |
||||
|
LA2503 |
u, h, l-2, tv, ag |
||||
|
LA2504* |
u, h, t, nd, ag |
||||
|
LA2505 |
u, l-2, t, ag, Xa |
||||
|
LA2506 |
ag, h, l-2, oli, tv |
||||
|
LA2507 |
h, t, nd, ag |
||||
|
LA2508 |
h, t, ag, Xa |
||||
|
LA2509 |
oli, l-2, tv, ag (wf) |
||||
|
LA2591 |
Xa-2, h, ag |
||||
|
LA2592 |
u, h, t, nd, ag |
||||
|
LA2593 |
u, auv, ag |
||||
|
LA4341 |
h, hy, u |
||||
|
Chromosome 11 |
|||||
|
LA0259 |
hl, a |
||||
|
LA0291 |
hl, a (ms-2) |
||||
|
LA0729 |
neg, a |
||||
|
LA0730 |
a, pro |
||||
|
LA0761 |
a, hl, j |
||||
|
LA0798 |
a, hl, j (ms-2) |
||||
|
LA0803 |
hl, a, pro (ms-2) |
||||
|
LA0881 |
neg, hl, a |
||||
|
LA0925* |
j, hl, a, f |
||||
|
LA1102 |
a, hl, tab |
||||
|
LA1109 |
j, hl, mnt |
||||
|
LA1488 |
neg, ini |
||||
|
LA1786 |
j, f, a, bi (c) |
||||
|
LA2352 |
j, f (p, c) |
||||
|
LA2364 |
j, a, f (y, wt, c, l, u) |
||||
|
LA2489 |
negne-2, a |
||||
|
LA4290 |
a, bks |
||||
|
LA4291 |
a, bks2 |
||||
|
LA4292 |
j-2, up, wv-3 |
||||
|
LA4344 |
a, mon |
||||
|
Chromosome 12 |
|||||
|
LA1111 |
fd, alb |
||||
|
LA1171 |
yg-2aud, fd |
||||
|
LA1177* |
alb, mua |
||||
6.2. Linkage Screening Testers (13)
The following set of linkage testers each combines two pairs of strategically situated markers on two different chromosomes (see TGC 22: 24). They are intended primarily for assigning new, unmapped markers to a chromosome. The more complete chromosome marker combinations (list 6.1 above) should be used for subsequent testing to delimit loci more accurately. Whereas six of these stocks should pretty well cover the tomato genome, we list below the entire series of the current available testers because alternative stocks differ in their usefulness, depending upon the phenotype of the new mutant to be located. The chromosomal location of each pair of markers is indicated in parentheses.
|
Access. |
Genotype |
|
LA0780 |
yv, c (chr 6); h, ag (chr 10) |
|
LA0781 |
ful, e (chr 4); neg, a (chr 11) |
|
LA0784 |
ful, e (chr 4); hl, a (chr 11) |
|
LA0982 |
clau, e (chr 4); hl, a (chr 11) |
|
LA0983 |
l, dl (chr 8); ah, marm (chr 9) |
|
LA1164 |
var, not (chr 7); ah, marm (chr 9) |
|
LA1166 |
clau, su3 (chr 4); icn, ag (chr 10) |
|
LA1182 |
sy, sf (chr 3); alb, mua (chr 12) |
|
LA1441 |
coa, c (chr 6); hl, a (chr 11) |
|
LA1443 |
scf, dgt (chr 1); l, al (chr 8) |
|
LA1444 |
wv, d (chr 2); af, tf (chr 5) |
|
LA1491 |
scf, dgt (chr 1); spa, ae (chr 8) |
|
1665 |
scf, dgt (chr 1); l, ae (chr 8) |
6.3. Miscellaneous Marker Combinations (288)
The following list groups stocks in which various mutant genes have been combined for various purposes. A few of these items include linked genes, but are classified here because other linkage testers provide the same combinations or because they are more useful as markers of several chromosomes. Some multiple marker combinations that are of limited usefulness, difficult to maintain, and/or redundant with other genotypes, have been dropped from the current list.
|
Access. |
Genotype |
|
LA0013 |
a, c, d, l, r, y |
|
LA0014 |
al, d, dm, f, j, wt, h |
|
LA0052 |
j, wt, br |
|
LA0085 |
Wo, d, h |
|
LA0137 |
dl, wd, gq |
|
LA0154 |
u, d, sp, h |
|
LA0157 |
d, m, p, r, y |
|
LA0158 |
t, u, Xa, y |
|
LA0159 |
a, e, mc, t, u, y, wf |
|
LA0169 |
ps, wf, wt |
|
LA0189 |
bl, cl-2 |
|
LA0190 |
wf, br, bk |
|
LA0215 |
at, y, u |
|
LA0281 |
e, t, u |
|
LA0296 |
br, bk, wf |
|
LA0297 |
tf, ug, Nr |
|
LA0299 |
ag, rv |
|
LA0345 |
ch, j-2 |
|
LA0497 |
ch, j-2, sf |
|
LA0499 |
Od, sn, at, cm/+ |
|
LA0508 |
gf, d, c, a, r, y |
|
LA0638 |
ht, d, r |
|
LA0648 |
rv, e, Wo, wf, j, h |
|
LA0719 |
Jau, clau |
|
LA0727 |
wv, d, c, r |
|
LA0728 |
a, lut |
|
LA0759 |
lg, vi, pe, t |
|
LA0760 |
lg, vi |
|
LA0770 |
clau, pa |
|
LA0775 |
tf, h, au, +/d |
|
LA0801 |
atv, slx |
|
LA0875 |
hp, u, sp |
|
LA0876 |
hp, sp |
|
LA0895 |
tp, sp, u, Hr |
|
LA0907 |
lut, pr |
|
LA0908 |
per, var |
|
LA0909 |
con, sf |
|
LA0912 |
ht, su3 |
|
LA0913 |
ful, su3, ht |
|
LA0914 |
com, ful |
|
LA0991 |
ful, e, com |
|
LA0995 |
deb, um |
|
LA0996 |
um, ig |
|
LA1018 |
h, Od, ptb |
|
LA1038 |
e, ht, su |
|
LA1072 |
sy, sf, um |
|
LA1078 |
ria, ves-2 |
|
LA1079 |
c, ves-2 |
|
LA1105 |
con, cur |
|
LA1106 |
fsc, ah |
|
LA1163 |
wv, d, tf |
|
LA1170 |
cn, con |
|
LA1219 |
d, u |
|
LA1663 |
Ln, Wom |
|
LA1664 |
hp, Ip |
|
LA1783 |
ad, sp |
|
LA1787 |
Bk-2, en |
|
LA1789 |
slcs, a |
|
LA1796 |
Rs, d, h |
|
LA1804 |
sr, sp, u |
|
LA1805 |
sr, y |
|
LA1806 |
ti, y, wf, al, j |
|
LA2349 |
p, d, r, wt, j, f |
|
LA2350 |
y, ne, p, c, sp, a |
|
LA2351 |
c, l, u, h |
|
LA2353 |
y, wt, n |
|
LA2355 |
sp, ug |
|
LA2360 |
e, wt, l, u |
|
LA2363 |
y, Wo, wt, c, t, j |
|
LA2369 |
p, Tm-1 |
|
LA2370 |
wf, n, gs |
|
LA2372 |
sp, fl |
|
LA2441 |
d, m-2, mc, rvt, t, u |
|
LA2452 |
B, f, gf, y |
|
LA2453 |
Gr, u |
|
LA2454 |
negne-2, u |
|
LA2457 |
u, so |
|
LA2458 |
Pto, sp, u |
|
LA2461 |
sp, stu, u |
|
LA2464 |
aer-2, r, upg, y |
|
LA2465 |
sp, u, v-2 |
|
LA2466 |
d, t, v-3 |
|
LA2467 |
pe, u, vi |
|
LA2473 |
alb, c, gra, sft |
|
LA2477 |
vo, cjf, wf, sp, l, u, h |
|
LA2478 |
aeafr, r, gs, h |
|
LA2486 |
inc, pds, sp, u, t |
|
LA2490 |
pdw, mc, pst, dl |
|
LA2492 |
ti, wf, e, mc, u, a |
|
LA2524 |
af, sd |
|
LA2526 |
dp, sp, u |
|
LA2527 |
l allele, sp, u |
|
LA2595 |
br, d, dm, wt, al, h, j, f |
|
LA2597 |
y, r, wf, mc, m-2, c, gs, gf, marm , h |
|
LA2797 |
bu, j |
|
LA3128 |
Ln, t, up |
|
LA3212 |
tmf, d, sp, u |
|
LA3217 |
glg, Pts |
|
LA3250 |
t, u |
|
LA3251 |
Del, y |
|
LA3252 |
Del, t |
|
LA3254 |
a, c, I, Ve |
|
LA3256 |
at, t |
|
LA3257 |
gf, gs, r |
|
LA3258 |
u, Ve |
|
LA3261 |
Del, gs |
|
LA3262 |
Del, ug |
|
LA3267 |
Cf-4, u |
|
LA3268 |
Tm-2, nv, u |
|
LA3269 |
Tm-1, u |
|
LA3271 |
Cf-?, Tm-1, u |
|
LA3273 |
Gp, Tm-22 |
|
LA3274 |
ah, Tm-2, nv, u |
|
LA3275 |
ah, Gp, Tm-22 |
|
LA3276 |
Tm-1, u, Ve |
|
LA3279 |
at, Del |
|
LA3284 |
at, gf |
|
LA3286 |
r, ug, y |
|
LA3287 |
hp, r, ug |
|
LA3288 |
hp, ug, y |
|
LA3289 |
gf, r, y |
|
LA3290 |
gf, hp, y |
|
LA3291 |
at, hp, t |
|
LA3292 |
Tm-2, u |
|
LA3294 |
bl, d, u |
|
LA3297 |
Tm-1, Tm-2, nv |
|
LA3299 |
ep, u |
|
LA3311 |
ogc, u |
|
LA3315 |
sp, pst, u, j-2, up, vo |
|
LA3362 |
gs, t |
|
LA3363 |
at, gs |
|
LA3364 |
gs, u |
|
LA3365 |
gf, gs |
|
LA3366 |
t, y |
|
LA3367 |
hp, t |
|
LA3368 |
hp, y |
|
LA3369 |
at, y |
|
LA3370 |
at, hp |
|
LA3371 |
hp, u |
|
LA3372 |
gs, y |
|
LA3373 |
at, u |
|
LA3374 |
u, y |
|
LA3375 |
gs, r |
|
LA3376 |
Del, hp |
|
LA3381 |
r, y |
|
LA3382 |
r, u |
|
LA3383 |
gs, hp |
|
LA3384 |
gf, y |
|
LA3385 |
gs, Nr |
|
LA3386 |
gf, t |
|
LA3387 |
Nr, t |
|
LA3389 |
Nr, y |
|
LA3390 |
Nr, ug |
|
LA3391 |
gf, hp |
|
LA3393 |
r, t |
|
LA3394 |
at, ug |
|
LA3395 |
gs, hp, y |
|
LA3396 |
at, u, y |
|
LA3397 |
gs, t, y |
|
LA3398 |
gs, hp ,t |
|
LA3399 |
at, gs, hp |
|
LA3400 |
at, hp, u |
|
LA3401 |
at, gs, y |
|
LA3402 |
hp, t, u |
|
LA3403 |
gf, gs, u |
|
LA3404 |
hp, u, y |
|
LA3405 |
gs, hp, u |
|
LA3406 |
at, hp, y |
|
LA3407 |
gs, u, y |
|
LA3408 |
t, u, y |
|
LA3409 |
gs, t, u |
|
LA3410 |
at, gs, u |
|
LA3411 |
gs, r, u |
|
LA3412 |
gf, gs, hp, u |
|
LA3413 |
at, gf |
|
LA3414 |
t, ug |
|
LA3415 |
ug, y |
|
LA3416 |
hp, ug |
|
LA3417 |
r, ug |
|
LA3418 |
gf, gs, ug |
|
LA3419 |
at, gf, gs |
|
LA3420 |
gf, ug |
|
LA3421 |
Nr, u |
|
LA3422 |
at, gs, ug |
|
LA3423 |
gf, gs, hp, u, y |
|
LA3424 |
gs, hp, u, y |
|
LA3425 |
gf, gs, hp, t, u |
|
LA3426 |
gs, hp, t, u |
|
LA3427 |
gf, gs, t, u |
|
LA3428 |
I, u, Ve |
|
LA3429 |
Del, gs, hp |
|
LA3432 |
Tm-1, Tm-2, nv, u |
|
LA3433 |
ah, Tm-2, nv, u |
|
LA3437 |
at, Nr |
|
LA3442 |
de, dil, u |
|
LA3443 |
cor, de, u |
|
LA3444 |
cor, dil, u |
|
LA3445 |
cor, pum, u |
|
LA3446 |
cor, sp, u |
|
LA3447 |
dil, sp, u |
|
LA3448 |
in, u |
|
LA3449 |
d, sp, u |
|
LA3450 |
bls, sp, u |
|
LA3451 |
bl, sp, u |
|
LA3540 |
I, u |
|
LA3541 |
gs, r, ug |
|
LA3542 |
u, ug |
|
LA3543 |
bls, o, u |
|
LA3545 |
Del, u, y |
|
LA3546 |
bls, Cf-?, u |
|
LA3547 |
ah, u |
|
LA3548 |
pum, u |
|
LA3549 |
bls, Gp, Tm-22, u |
|
LA3557 |
Del, gf |
|
LA3558 |
gf, Nr |
|
LA3559 |
Del, gs, y |
|
LA3561 |
gf, gs, hp, Nr, u |
|
LA3562 |
gf, gs, u, y |
|
LA3563 |
sp, u |
|
LA3585 |
gf, u, ug |
|
LA3586 |
t, u, ug |
|
LA3587 |
r, u, ug |
|
LA3589 |
u, ug, y |
|
LA3590 |
Nr, gs, y |
|
LA3591 |
Nr, u, y |
|
LA3593 |
hp, u, ug |
|
LA3594 |
gs, hp , ug |
|
LA3595 |
gf, hp, ug |
|
LA3596 |
hp, t, ug |
|
LA3597 |
at, hp, ug |
|
LA3598 |
r, t, ug |
|
LA3599 |
at, t, ug |
|
LA3600 |
t, ug, y |
|
LA3601 |
gf, r, t |
|
LA3603 |
at, gf, y |
|
LA3604 |
hp, r, t |
|
LA3605 |
at, ug, y |
|
LA3606 |
r, t, y |
|
LA3607 |
gs, hp, Nr |
|
LA3608 |
hp, Nr, t |
|
LA3609 |
hp, Nr, y |
|
LA3615 |
dx, u |
|
LA3675 |
hp, Nr, u |
|
LA3676 |
gf, hp, t |
|
LA3677 |
gf, hp, r |
|
LA3678 |
Nr, u, ug |
|
LA3679 |
gs, Nr, ug |
|
LA3680 |
Nr, t, u |
|
LA3682 |
gs, t, ug |
|
LA3683 |
gs, ug, y |
|
LA3684 |
Nr, t, y |
|
LA3686 |
gs, Nr, t |
|
LA3688 |
gf, gs, hp |
|
LA3689 |
gs, hp, r |
|
LA3691 |
r, u, y |
|
LA3692 |
at, r, y |
|
LA3693 |
g, t, u |
|
LA3694 |
Del, gs, u |
|
LA3695 |
Del, hp, t |
|
LA3697 |
gs, r, t |
|
LA3698 |
gs, r, y |
|
LA3699 |
gf, u, y |
|
LA3700 |
at, gf, u |
|
LA3701 |
at, t, u |
|
LA3702 |
gf, gs, y |
|
LA3703 |
gf, hp , u |
|
LA3704 |
at, gf, hp |
|
LA3706 |
at, gs, t |
|
LA3706 |
Del, t, y |
|
LA3709 |
Del, gf, gs, hp, u |
|
LA3741 |
pum, u |
|
LA3742 |
de, u |
|
LA3743 |
cor, u |
|
LA3744 |
sph, u |
|
LA3745 |
bl, u |
|
LA3771 |
hp, Bc |
|
LA3810 |
hp, t |
|
LA3811 |
gf, r |
|
LA3812 |
bls, Tm, Tm-2, nv |
|
LA3815 |
Del, t, ug |
|
LA3821 |
dil, pum, u |
|
LA3823 |
pum, sp, u |
|
LA3826 |
mon, u |
|
LA3827 |
dil, cor, sp, u |
|
LA3830 |
ep, Bc, u |
|
LA3831 |
gf, gs, r, y |
|
LA4136 |
Rg-1, r |
|
LA4342 |
oli, u, y |
|
LA4343 |
gq, h |
|
LA4348 |
yg-2, cint |
7. Provisional mutants (107).
The following group of provisional mutants are listed here, rather than with the monogenic stocks because they have not been fully characterized. For some, a monogenic segregation has not been verified, for others complementation tests were either not performed or did not detect allelism with existing mutants of similar phenotype. Most of these lines resulted from mutagenesis experiments, the remainder occurring spontaneously. Genetic background is indicated, if known. More information on these stocks is available at our website.
|
Access. |
Traits |
Phenotype |
Background |
|
2-293 |
Snout |
Fruits distorted, always snouted. |
S. Marzano |
|
2-305 |
Broad |
Leaves broader and more divided than Pearson, internodes shortened; fruits elongate. |
Pearson |
|
2-473 |
Yellow fruit, pale corolla |
Spontaneous mutant |
Red Cherry |
|
2-493 |
Purple tipped leaves, puny |
Miniature plant, reduced fruit set, parthencocarpic fruit. |
Peto 795 |
|
2-575 |
Poxed fruit |
Pox marks in radial lines, in ripe fruit = yellow or necrotic. |
PI 260395 |
|
2-585 |
Balloon |
Short internodes, leaves dark green, acuminate, extremely plicate and veins prominent; leaves broad and wavy, highly divided; flowers small, poorly opened; mostly parthenocarpic fruit. |
CP-2 |
|
2-621 |
Turbinate |
Flowers semiturbinate, corolla wavy, anthers semi-dialytic. |
VFN-8 |
|
2-625 |
Prolific leaves |
Leaves highly modified and proliferated, dark green. |
VFN-8 |
|
2-629 |
Me-oid |
Plant rank, most branches do not terminate, yet have sp gene; leaves ext. reduced with long terminal segment, laterals short and strongly recurved. |
VFN-8 |
|
2-633 |
Hooded flowers |
Corolla funneliform as a result of corolla segments being joing distally more than normal. |
breeding line |
|
2-643 |
Yellow green |
Whole plant yellow green, moderate vigor, good fruit set. Similar to fy and yt genes. |
VF36 |
|
3-003 |
yv-oid |
Yellow green cots, very chlorotic leaves, later chlorosis is general, strong anthocyanin. In field, entirely normal. |
VF36 |
|
3-055 |
Round cotelydons and leaves |
Chlorotic interveinal regions, normal vigor, short round cots. |
VF36 |
|
3-073 |
Abnormal flowers |
Calyx and corolla segments enlarged; stamens deformed, dialytic and petaloid; pistil fasciated, distorted. |
VF36 |
|
3-077 |
Dwarf |
Slow, dwarf, broad recurved leaves, heavy stems, short internodes. Leaves dark green, strongly recurved at tips of all segments, not rugose. As brittle as hl. |
VF36 |
|
3-082 |
Dwarf |
Short stocky dwarf, recurved leaves. Leaves not rugose or stiff, but strongly recurved. Good expression at seedling stage. |
VF36 |
|
3-083 |
Yellow virescent |
Bright yellow virescent, paler later. |
VF36 |
|
3-084 |
Yellow green |
Leaves overall yellow green, becoming speckled green. |
VF36 |
|
3-088 |
Light green, dark veins |
Light green, miniature stature. |
VF36 |
|
3-097 |
Yellow green |
Yellow green, narrow leaves, entire margins. |
VF36 |
|
3-098 |
Slow chlorotic |
Slow chlorotic, yellow green leaves, not fully divided (clavate). |
VF36 |
|
3-101 |
tl mimic |
Probably an allele of tl, complete response to thiamine application. |
VF36 |
|
3-106 |
Strong anthocyanin |
Strong anthocyanin under leaf, slow slender and erect. |
VF36 |
|
3-107 |
Bright yellow virescent |
Bright yellow virescent leaves. |
VF36 |
|
3-112 |
Crippled |
Leaf rugose, rough, variegated dark green / grey green; older leaves deformed. |
VF36 |
|
3-115 |
rv-oid |
Overall light green leaves with dark veins; stunted, narrow segments. |
VF36 |
|
3-118 |
Rugose recurved leaves |
Leaves rugose, recurved; plant dwarfish, 2/3 size. |
VF36 |
|
3-127 |
Bright yellow |
Overall bright yellow, plant 2/3 size. |
VF36 |
|
3-241-1 |
Yellow, anthocyanin |
Overall yellow, anthocyanin on stem. |
VF36 |
|
3-243 |
Long narrow |
Long narrow twisted leaves, anthocyanin on stem. Entire, narrow segments, suggesting triplo-3., flowers with elongate parts. |
VF36 |
|
3-303 |
Slow, narrow leaves |
Very slow,(1/10), yellow green virescent, leaves narrow and acute, deep dark veins |
Moneymaker |
|
3-305 |
La-mimic |
Identical with La in all respects, except leaves more subdivided. |
Moneymaker |
|
3-307 |
Broad, grey green |
Seedling dwarf, cotyledons and leaves broad, light grey green leaves very convex, deep veined. Mature plant normal size, leaves reduced, slightly chlorotic interveinally, bullate, few fruits set. |
Moneymaker |
|
3-309 |
Bunchy growth, mitten leaves |
Seedling dwarf, (1/3 size) short internodes, leaves abbreviated, mitten shaped. Same phenotype in mature plant. |
Moneymaker |
|
3-311 |
Slow, rugose |
Seedling extremely slow (1/20), leaves with fewer segments, very rugose, dark green. |
Moneymaker |
|
3-315 |
Glossy dwarf |
Extreme dwarf (1/10 size), dark glossy green, like d^x. |
Moneymaker |
|
3-317 |
ra-oid |
2/3 size, leaves rounded, convex,recurved, resembles rava. Flowers tiny, hooded, set few fruit. |
Moneymaker |
|
3-319 |
Striated, divided |
1/3 size, cotyledons and leaves variably striated, leaves short, convex, recurved, well divided and variably deformed, leaves dark green, variably bullate, twisted and deformed flowers, very few fruit set. |
Moneymaker |
|
3-321 |
Narrow, dissected |
Cotyledons narrow, small elliptical; leaves narrow, deeply serrated, surface irregular, turning grey-green, small flowers, scattered fruit set. |
Moneymaker |
|
3-323 |
Spirally coiled |
1/3 size, cotyledons ext. narrow, leaves spirally coiled and large; plant gets all wrapped up in itself, leaves very dark green, rugose and dentate. |
Moneymaker |
|
3-325 |
Short, yv |
Dwarf, short internodes (1/3), leaves and cotyledons broad, leaves slightly paler with deep veins. Mature plant (GH only): very short compact, yv like, extreme distinct. |
Moneymaker |
|
3-329 |
Bronzing |
Dwarf (1/5 size), cotyledons and leaves large, leaves broad and convex, later bronzing interveinally, flowers tiny. |
Moneymaker |
|
3-331 |
Serrated leaves |
Leaves extremely narrow, deeply serrated like acl. Mature plant 1/3 size, tiny dark green plicate leaves, dainty appearance, flowers hooded. |
Moneymaker |
|
3-335 |
Gold dust virescent |
1/3 size, bright yellow virescent (gold dust), Narrow acute leaves with deep veins |
Moneymaker |
|
3-337 |
Glossy dwarf |
Leaves short, smooth and glossy, compact (1/20 size) plant, delayed flowering. |
Moneymaker |
|
3-341 |
Dwarf |
Dwarf stature (1/2 size), very short internodes, concave leaves, deep veins, interveinal chlorosis, leaf segments small and few, flowers small. |
Moneymaker |
|
3-403 |
Fimbriate leaves |
Two plants with fimbriate leaves, like nv (from Epstein 516) |
VF36 |
|
3-404 |
Speckled white |
Fine white marginal speckling, nearly normal size. |
VF36 |
|
3-405 |
Streaked virescent |
2\3 size, streaked cotelydons, strong yellow green virescence. |
VF36 |
|
3-406 |
Streaked variegated |
Large size, streaked and variegated, extremly irregular, like "crippled" |
VF36 |
|
3-408 |
bu mimic |
Early seedlings show bunch habit with extremely short internodes, almost rosette like; exceeds bu in compactness |
VF36 |
|
3-411 |
Blue green; bushy roots |
1/4 size, dark blue green, streaked anthocyanin of leaf undersides; bushy roots, dense growth of solely twisted lateral roots |
VF36 |
|
3-423 |
ra-oid |
Slender seedling with grey-green colour and recurved leaves. Slow (1/3 normal). Prominent silky hairs of type ra syndrome, like 3-318 |
VF36 |
|
3-424 |
Extreme dwarf |
Extreme dwarf with type d syndrome; intermediate between dd and d:x in stature |
VF36 |
|
3-434 |
d^cr like |
Dwarf like allele of d:cr, except leaves are more obtuse, broader, and more ruffled |
VF36 |
|
3-436 |
Overall yellow |
Uniformly overall yellow like au and var. |
VF36 |
|
3-441 |
Singed hairs |
Nearly normal size, also hairless with less suppressed hairs above cotyledons, like singed |
VF36 |
|
3-601 |
clau mimic |
Resembles clausa, but F1 allele test shows not allelic. |
VFNT Ch |
|
3-612 |
wiry mimic |
Resembles wiry, strong expression. |
VFNT Ch |
|
3-613 |
La mimic |
Segregates as a dominant La mimic in M2. Also segregates for a dgt-like mutant. |
VFNT Ch |
|
3-614 |
pds-oid |
Short, stocky, 1/4 size, light green, not much like pds. |
VFNT Ch |
|
3-617 |
Dwarf |
Dwarf like, not allelic with d, linked to bip but not Wo. |
VFNT Ch |
|
3-618 |
mimic of a |
Reduced anthocyanins. |
VFNT Ch |
|
3-619 |
wiry mimic |
VFNT Ch |
|
|
3-621 |
d mimic |
Typical d syndrome, though more extreme, but not allelic with d. |
VFNT Ch |
|
3-622 |
d mimic |
Typical d syndrome, but not allelic with d. |
VFNT Ch |
|
3-624B |
Yellow virescent |
VFNT Ch |
|
|
LA0506 |
Triplo-8 mimic |
Triplo-8 mimic, ex. 2-72. Maybe dominant deficiency transmitted through egg, not pollen. |
S. Marzano |
|
LA0652 |
calycine poxed |
Spotting is pox. Calycine trait is allele of ch. Both spotting and calycine appear as dominants. |
|
|
LA0739 |
ag mimic |
allele of ag? |
|
|
LA0765 |
Acute leaves |
Acute leaves. |
|
|
LA0791 |
Long John |
Originated from crosses among pear types. Elongate fruit shape segregates about 120 long : 48 + in F2's with wild type. |
|
|
LA0801 |
Pseudopolyploid |
||
|
LA0870 |
frizzled virescent |
||
|
LA0871 |
Calico |
||
|
LA1012 |
Mottled, chlorotic petiole |
Also segregates for dl, l. |
|
|
LA1060 |
spl-oid |
Derived from hg x (sy sf) F2; bright yellow interveinal areas, leaves strongly rolled and reducded especially at growing point. |
|
|
LA1065 |
Miniature |
Derived from pic x (ag h, c yv) F2. Phenotype like rmt, leaves reduced and strongly plicate, 1/3 size plant. |
|
|
LA1066 |
Speckled |
Speckled mutant derived from lutea, small darker colored seedling, tiny lighter colored specklings, closely resembles pun, probably allelic. |
|
|
LA1095 |
fy-oid |
Low grade yg chlorophyll deficiency, uniform over plant; expr. stronger in field. |
Rutgers |
|
LA1098 |
Multiple inflor. |
Proliferated and elongate inflorescence, in sp line. |
|
|
LA1144 |
ful mimic |
Uniform strong yg, like ful. |
Earlipak 7 |
|
LA1148 |
Light green |
Light yellow green, normal vigor, poor expression in seedling. |
VF145 7879 |
|
LA1149 |
Xanthoid |
Bright yellow, stronger at growing point, segregates 2 normal, 1 Xanthoid, 1 chlorotic lethal. |
|
|
LA1154 |
pale virescent, twisted leaves |
Pale virescent, twisted leaves; strongly chlorotic growing point, green at first, turning pale, almost whitish; extremely slow (1/10+ normal); twisted and distorted cotyledons. |
|
|
LA1160 |
Fused cotyledons |
Cotyledons fused along the proximal part of the margins, net effect suggesting cot’s of morning glory. |
|
|
LA1193 |
Yellow-sectored |
Extremely stunted and sterile in field. |
|
|
LA1201 |
rv-oid |
||
|
LA1202 |
Dirty orange cherry |
||
|
LA1436 |
Withered cotyledons |
Withered cotyledons, slow (1/3 size), compact seedling, strong yellow virescent, older leaves are strongly yellow green. |
|
|
LA1494 |
Adventitious roots |
||
|
LA1532 |
rv-oid |
Clearly defined, useful seedling marker. |
VF145-7879 |
|
LA1533 |
Purple stem |
Incompletely dominant, Early seedlings not well distinguished, later moderately intense purpling, especially on leaf veins on undersides. |
|
|
LA1707 |
Short stature |
Not true dwarf phenotype; good vigor and distinct in seedling stage. |
VF145-7879 |
|
LA2018 |
Anthocyanin deficient |
No anthocyanin at any stage. |
Niagara |
|
LA2019 |
Virescent tangerine mimic |
Homozygous for phenotype exactly like t^v. Jointless, very firm fruit, determinate canning type vine, vigorous. |
|
|
LA2020 |
Dark green foliage |
Dark geen foliage; fruit 10-12 locules, catfaced, yellow skin and red flesh. |
|
|
LA2021 |
Variegated yellow |
Very slow and stunted; variegated yellow in large patches over most of the older foliage. Seedling: bright yellow green, the yellow spots turning to white. |
|
|
LA2358 |
Marginal leaf chlorosis |
||
|
LA2375 |
Lc- reduced locule |
May not be monogenic, possibly pleiotropic effect of pear shape (ovate gene). |
|
|
LA2806 |
Incomplete anthocyanin mutant |
Grey green hypocotyl, similar to ai and pai, but darker. Spontaneous mutant. |
Vis |
|
LA2817 |
lg mimic |
lg mutant, possibly allelic |
|
|
LA2897 |
Virescent gold top |
||
|
LA2899 |
Wrinkled fruit |
||
|
LA3851 |
Virescent |
R.Ruhm |