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Epigenetic Control May Explain Large Within-Plant Heterogeneity of Meiotic Behavior in Telocentric Trisomics of Rye

机译:表观遗传控制可能解释黑麦远心三体组中减数分裂行为的大的植物内异质性。

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摘要

In telocentric trisomics (telotrisomics) of organisms in which the chromosomes normally have two distinct arms, a single chromosome arm with a centromere is present in addition to a complete diploid set of chromosomes. It is the simplest form of polysomy and suitable for analyzing meiotic pairing and recombination patterns in situations where chromosomes compete for pairing. When no suitable meiotic chromosome markers are available, four metaphase I configurations can be distinguished. Their relative frequencies are indicative of the pairing and recombination patterns. In short arm (1RS) telotrisomics of chromosome 1R of rye (Secale cereale) we observed great differences in pairing and recombination patterns among spikes from different tillers and clones of the same plants. Anthers within spikes were only very rarely different. We analyzed a large number of genotypes, including inbreds as well as hybrids. The effects of genetic and environmental conditions on heterogeneity, if any, were limited. Considering that the reproductive tissue of a spike is derived from one primordial cell, it seems that at the start of sexual differentiation there was variation among cells in chromosomal control, which at meiosis determines pairing and crossing-over competence. We suggest that it is an epigenetic system that rigidly maintains this pattern through generative differentiation. In competitive situations the combination most competent for pairing will pair preferentially, forming specific meiotic configurations with different frequencies for different spikes of the same plant. This would explain the heterogeneity between spikes and the homogeneity within spikes. The epigenetic system could involve chromatin conformation or DNA methylation. There were no signs of heterochromatinization.
机译:在染色体通常具有两个不同臂的有机体的三体三体组学(telotrisomics)中,除了完整的二倍体染色体组外,还存在带有着丝粒的单个染色体臂。它是最简单的多态性形式,适合在染色体竞争配对的情况下分析减数分裂配对和重组模式。当没有合适的减数分裂染色体标记可用时,可以区分四个中期I构型。它们的相对频率指示配对和重组模式。在黑麦(Secale graine)1R染色体的短臂(1RS)端粒组学中,我们观察到来自同一植物不同分till和克隆的穗之间的配对和重组模式存在很大差异。尖峰内的花药几乎没有什么不同。我们分析了许多基因型,包括近交和杂种。遗传和环境条件对异质性的影响(如果有的话)是有限的。考虑到穗状花序的生殖组织来自一个原始细胞,似乎在性别分化开始时,染色体控制中的细胞之间存在差异,减数分裂时这决定了配对和交叉能力。我们建议这是一个表观遗传系统,通过生成分化严格地维持这种模式。在竞争情况下,最有能力配对的组合将优先配对,从而针对同一植物的不同穗形成具有不同频率的特定减数分裂构型。这将解释峰值之间的异质性和峰值内部的均质性。表观遗传系统可能涉及染色质构象或DNA甲基化。没有异染色质的迹象。

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