Effect of three anthocyaninless genes on seed aging in tomato (Lycopersicon esculentum Mill.) Balacheva, E. and Atanassova, B. Institute of Genetics, Bulgarian Academy of Sciences, Sofia 1113, Bulgaria In   our   previous   studies   it   was   found   that   three   anthocyaninless   mutants   of   tomato, anthocyaninless   of   Hoffmann   (ah),   anthocyanin   without   (aw)   and   baby   lea   syndrome   (bls), germinated more rapidly than the wild type lines under both, optimal and a relatively large scale of stress conditions (Atanassova et al., 1997 a, b). In order to establish whether the effect of the three genes   concern   other   seed   characteristics,   (other   than   velocity   of   germination)   we   designed experiments aimed at studying the longevity of the mutant and wild type seeds.   The investigation was performed on isogenic/near isogenic lines (IL/NIL) (NIL) described by Maxon-Smith   and   Ritchie   (1982)   and   Philouze   (1991),   on   seed   dry-stored   under   laboratory temperature and humidity.   As  it  can  be  seen  from  the  results  presented  in  Table  1,  the  initial  quality  of  the  seed, examined  a  few  months  after  seed  production  was  high.  Mutant  seeds  germinated  more  rapidly than the wild type ones and the differences in the  time to 50% germination between them varied depending on the genotype. The same applied to seed stored for one, two or three years (data for the  first  and  second  year  of  storage  not  presented  as  no  significant  differences  in  germination responses between the seed produced throughout these three years had occurred).   Germination  responses  after  four  and  five  years  of  seed  storage  clearly  demonstrated difference in tolerance to storage between the wild type and mutant seeds. After four years of seed storage the time to 50% germination in the anthocyaninless IL/NILs was equal or longer than that in the wild type ones, and after five years of storage all wild type genotypes germinated more rapidly than  the  mutant  ones.  Aging  in  the  mutant  seeds  resulted  also  in  significant  decrease  in  seed viability expressed as percentage of germination, while in Porphyre and Ailsa Craig after four years of storage and in Apedice and Ailsa Craig after five years of storage differences in the percentage of germination between aged and non-aged seeds were not significant.   Study of seed coat morphology and histochemistry provided evidence that the three mutant alleles  ah,  aw  and  bls  not  only  completely  inhibited  anthocyanin  biosynthesis,  but  were  also associated with alterations in seed morphology and testa histochemistry (Atanassova et al., 2004). It was found that wild type seeds possessed longer hairs than  ah  and  bls  mutant seeds. The aw seeds were a dark yellowish-beige color, while wild type ones were light beige. The inner epidermal testa   layer   of   the   three   wild   type   genotypes   contained   condensed   tannins   while   in   the anthocyaninless  genotypes  this  compound  was  absent.  Condensed  tannins  contribute  to  the rigidification of cell structure (Haslam, 1993). Therefore their absence in seed coats could contribute to  its  increased  permeability  that  subsequently  could  lead  to  the  more  rapid  water  uptake  and germination observed in the mutant seeds (Atanassova et al., 1997 a, 2004).  On the other hand, according  to  Hedin  and  Waage  (1986),  Oigiangbe  and  Onigbinde  (1996)  condensed  tannins  are important in plant tissue because they probably inhibit microbial invasion and growth of pathogens and  contribute  to  the  resistance  to  infestation  by  insects.  As  the  results  presented  in  Table  1 showed  that  the  mutant  seeds  possessed  lower  tolerance  to  storage  than  the  wild  type  ones,  it might be assumed that the absence of condensed tannins in the mutant seed coat is the main seed characteristic contributing to the reduced vigor and viability of aged mutant seeds. Table 1.Germination responses of aged seeds of tomato IL/NILs differing in genes ah, aw and bls Genotype Time to 50%    Germination(%)    Time to 50% Germination

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