The recessive spontaneous sy18 mutation with nonhomologous synapsis was mapped in rye. The sy18 gene was located in the centromeric region of chromosome 2R in relation to three rye SSR (simple sequence repeats) loci, i.e.
View Article and Find Full Text PDFA study was made of the expression and inheritance of the sy11 mutation, which alters homologous chromosome synapsis in meiotic prophase I of rye. The abnormal phenotype proved to be determined by a recessive allele of a single sy11 gene. Univalents and multivalents were observed in homozygotes for the mutant allele.
View Article and Find Full Text PDFStudies of phenotypical expression of synaptic mutations in combination with the localization of corresponding genes on a genetic map permit individual stages of the meiotic process to be differentiated. Two rye asynaptic genes, sy1 and sy9, were mapped with the use of microsatellite markers (SSR) in the pericentromeric regions of the long chromosome arms 7R and 2R, respectively. The sy9 gene cosegregated with two SSR markers Xscm43 and Xgwm132.
View Article and Find Full Text PDFAExpression and inheritance of the sy18 mutation causing impairment of synapsis homology were studied. It was established that the abnormal phenotype is determined by a recessive allele of the sy18 gene. Univalents and multivalents are observed in homozygotes for this mutant allele.
View Article and Find Full Text PDFPostzygotic reproductive isolation, based on negative interactions of genes, is a key aspect of divergent speciation in plants and animals. The effect of the interaction manifests as a drastic reduction in fitness of hybrids of the first and subsequent generations, which is expressed as hybrid lethality, weakness or sterility. Both simple genetic control of genetic incompatibility, which includes interallelic negative complementation or epistatic interactions of a limited number of genes, and more complex control, based on epistatic interactions of many genes, have been described in plants.
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