Synapsis and chiasma formation were studied in pollen mother cells of four meiotic mutants of tomato. The four mutants displayed defects in the assembly of the synaptonemal complex (SC) covering the whole range from almost complete absence of synapsis to complete synapsis at pachytene. In three mutants, we found a good correlation between the number of bivalents connected by at least one tripartite SC segment at pachytene and the number of chiasmatic bivalents at metaphase I. We suggest that in tomato functional chiasmata are only formed in the context of the tripartite SC.
Synapsis and chiasma formation were analyzed in a ditelo-substituted haploid of rye (Secale cereale), in which chromosome 1R was replaced by its telosomes. The study was made by comparing synaptonemal complex formation at early meiotic prophase I, chromosome associations at metaphase I, and recombinant chromosomes at anaphase I and prophase II. For the analysis of synaptonemal complexes, 41 nuclei at stages ranging from leptotene to early diplotene were selected. In the leptotene and early zygotene nuclei, numerous alignments of axial cores involving the same or different chromosomes were observed. Pairing initiation sites occurred at both interstitial and distal segments. Throughout zygotene the extent of pairing gradually increases, with values up to 84.8% at a stage that is morphologically comparable with late pachytene. Pairing-partner exchanges were frequently observed in zygotene nuclei, giving rise to multiple associations encompassing all or most of the chromosomes. In cells at metaphase I multivalents were very rare (2%), indicating elimination of most pairing-partner exchanges. In cells at metaphase I, anaphase I, and prophase II chromosome length, centromere position, and C-banding pattern enable the identification of the chromosomes 1RS, 1RL, 4R, 5R, and 6R, and the distinction of three metacentric chromosomes (RM1, RM2, and RM3). Metaphase I bonds were found to be nonrandomly distributed. Associations between the arms 4RL, 5RL, 6RL, and RM1L, all of them without telomeric C-bands, were more frequent than between the remaining arms. The bonds were mainly located at the distal parts of the chromosomes. The frequency of recombinant chromosomes at anaphase I or prophase II suggests that metaphase I bonds were true chiasmata.Key words: Secale cereale, haploid, synaptonemal complex, chiasmate bonds, C-banding.
Female meiosis was analysed in squash preparations of ovules from three meiotic mutants and wild-type plants of tomato. In the completely asynaptic mutant as6, chromosome pairing and chiasma formation were virtually absent in both sexes. In the partially asynaptic mutant asb, with intermediate levels of chromosome pairing at pachytene, there were a higher number of chiasmate chromosome arms in female meiosis than in male meiosis, whereas in the desynaptic mutant as5 there were normal levels of chromosome pairing at pachytene and a similar reduction in chiasma frequency in the two sexes. In wild-type tomato, we found slightly higher numbers of chiasmate chromosome arms in female meiosis than in male meiosis. We propose that the higher female chiasma frequencies in mutant asb and wild-type tomato result from a longer duration of female meiotic prophase. This would allow chromosomes more time to pair and recombine. It is possible that a longer duration of prophase I does not affect mutants as5 and as6, either because the meiotic defect acts before the pairing process begins (in as6) or because it acts at a later stage and involves chiasma maintenance (in as5).
Ten cytoplasmic male sterile (CMS) sunflower (Helianthus annuus L .) lines were crossed with nine maintainer or male fertility restorer lines in a diallel crossing scheme . Based on fertility restoration of the F, generation, CMS lines were divided into four groups . At least two new sources of CMS, CMS PET2 and CMS GIG1, were found to be potentially useful for commercial production of hybrids . Environment had an influence on fertility restoration of one CMS line, CMS MAX1 . Effective restoration of male fertility for CMS RIG1, CMS ANN2, and CMS ANN3 was not found .
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