Chromosome
location
of
tomato
ESTs
related
to
carbon
metabolism
)
MR
Physiologie
et
Biotechnologie
Végétales
IBVI
-
INRA
BP
81
-
33
883
Villenave
d'Ornon
-
Cedex
(France)
I
didate
genes
linked
to
sugar/acid
metabolism
content
in
to
n
h
tomato
EST
database
(h
ww
.
he
a
h
a
u
the
p
o
.
el
L
.
esculentum
w
the
genome
to
be
segmented
(Pan
et
a
.
n
was
connected
to
the
high
-
density
map
of
tomato
(Tanksley
et
al
99
)
by
pro
ing
all
the
ILs
wi
e
m
ening
f
ing
four
restriction
enzymes
(EcoRI,
EcoRV,
Hind
III,
and
XbaI)
.
Genomic
DNA
extraction,
digestion,
b
re
as
d
i
mbani
et
)
w
ls
e
n
an
Colombani
et
al,
2000)
and
their
l
was
ro
m
y
e
m
m
d
hey
ted
ly
,
h
metabolism,
ement
as
te
g
related
to
e
d
References
Es
sion
line
population
of
Lycopersicon
pennellii
in
the
ted
s
the
id
ld
.
cs
Liu
n
O
,
Z
D
)
rati
nucleo
ene
d
a
A
p
309
-
322
ma
e
o
e
43:
29
-
40
SD,
Ganal
MW,
Prince
JP
n
r
u
,
nno
r
e
R
ler
L,
Paterson
AH,
Pinedo
O,
Roder
MS,
Wing
RA,
Wu
W,
Young
ND
(1992)
High
density
molecular
linkage
of
t
ge
1
P
.
Duffe
(1),
M
.
C
.
Gomez
(1),
D
.
Just
(2),
M
.
Lemaire
-
Chamley
(2),
C
.
Rothan
(2),
and
M
.
Causse
(1)
(1)
INRA
Unité
de
Génétique
et
Amelioration
des
Fruits
et
Légumes
-
BP
94
-
84143
ontfavet
-
Cedex
(France)
M
(2
U
n
order
to
screen
for
putative
can
fru
48
mato
it,
we
selected
EST
clo
es
in
t
e
TIGR
ttp://w
tigr
.
org/tdb/tgi/lgi/)
.
T
se
clones
were
loc
ted
on
t
e
tom
to
map
sing
opulation
f
introgression
lines
(ILs)
having
one
segment
of
L
penn
lii
(LA716)
in
a
(M82)
background
(Eshed
and
Zamir,
1995)
.
The
75
ILs
allo
into
107
bins
l,
2000;
http://www
.
sgn
.
cornell
.
edu/)
The
IL
populatio
,
1
2
b
th
the
RFLP
markers
from
the
framework
F2
map
(Pan
et
al,
2000)
.
The
ESTs
wer
apped
by
RFLP
after
scre
or
polymorphism
us
and
hy
ridization
we
escribed
n
Saliba
-
Colo
al
(2000
.
A
few
ESTs
ere
a
o
mapp
d
i
intraspecific
population
(Saliba
-
ocation
in
the
IL
map
deduced
f
m
the
common
RFLP
arkers
.
All
fourt
ight
ESTs
involved
in
carbon
metabolis
were
appe
(Table
1)
.
T
represen
enzymes
involved
in
transport
and
a
few
oth
Calvin
cyc
er
functions
.
They
revealed
57
le,
glyco
sis,
TCA
cycle
loci
.
Their
involv
sugar
and
starc
candida
enes
for
QTLs
carbon
m
tabolism
remains
to
be
stu
ied
.
hed
Y,
Zamir
D
(1995)
An
introgres
cultiva
tomato
enable
entification
and
fine
mapping
of
yie
-
associated
QTLs
Geneti
141:
1147
-
1162
Pan
Q,
Y
-
S,
Budai
-
Hadria
,
Sela
M
Carmel
-
Goren
L,
amir
,
Fluhr
R
.
(2000
Co
homologues
in
the
genomes
of
two
dicotyle
mpa
ve
genetics
of
tide
binding
site
-
leu
ons:
tom
cine
rich
to
and
repea
rabido
t
n
resista
sis
.
Genetics
155:
ce
g
Saliba
-
Colombani
V,
Causse
M,
Gervais
L,
Philouze
J
(2
m
000)
Efficiency
of
AFLP,
RAPD
and
RFLP
rkers
for
the
construction
of
an
intraspecific
ap
of
th
tomat
genome
.
Genom
Tanksley
,
de
Vice
te
MC,
Bonierbale
MW,
B
oun
P,
F
lton
TM
Giova
ni
JJ,
Grandillo
S,
Ma
tin
GB,
M
sseguer
,
Miller
JC,
Mil
maps
he
tomato
and
potato
nomes
.
Genetics
132:
1141
-
1
60
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