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Robertsonian chromosomes and the nuclear architecture of mouse meiotic prophase spermatocytes

机译:罗伯逊染色体和小鼠减数分裂前期精母细胞的核结构

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The?nuclear architecture of meiotic prophase spermatocytes is based on higher-order patterns of spatial associations among chromosomal domains from different bivalents. The meiotic?nuclear architecture?depends on the chromosome characteristics and consequently is prone to modification by chromosomal rearrangements. In this work, we consider Mus domesticus spermatocytes with diploid chromosome number 2n = 40, all telocentric, and investigate a possible modification of the ancestral nuclear architecture due to the emergence of derived Rb chromosomes, which may be present in the homozygous or heterozygous condition. In the 2n = 40 spermatocyte nuclei random associations mediated by pericentromeric heterochromatin among the 19 telocentric bivalents ocurr at the nuclear periphery. The observed frequency of associations among them, made distinguishable by specific probes and FISH, seems to be the same for pairs that may or may not form Rb chromosomes. In the homozygote Rb 2n = 24 spermatocytes, associations also mediated by pericentromeric heterochromatin occur mainly between the three telocentric or the eight metacentric bivalents themselves. In heterozygote Rb 2n = 32 spermatocytes all heterochromatin is localized at the nuclear periphery, yet associations are mainly observed among the three telocentric bivalents and between the asynaptic axes of the trivalents. The Rb chromosomes pose sharp restrictions for interactions in the 2n = 24 and 2n = 32 spermatocytes, as compared to the ample?possibilities for?interactions between bivalents in the 2n = 40 spermatocytes. Undoubtedly the emergence of Rb chromosomes changes the ancestral nuclear architecture of 2n = 40 spermatocytes since they establish new types of interactions among chromosomal domains, particularly through centromeric and heterochromatic regions at the nuclear periphery among telocentric and at the nuclear center among Rb metacentric ones.
机译:减数分裂前期精母细胞的核结构基于来自不同二价体的染色体结构域之间空间关联的高阶模式。减数分裂的核结构取决于染色体的特征,因此容易被染色体重排修饰。在这项工作中,我们考虑了二倍体染色体数为2n = 40的家鼠精子细胞,全部为端粒,并研究了由于衍生的Rb染色体的出现而可能对祖先核结构进行的修饰,而这些Rb染色体可能以纯合或杂合状态存在。在2n = 40的精母细胞核中,在核周边出现了19个端粒二价链之间的着丝粒异染色质介导的随机关联。通过特定的探针和FISH可以区分它们之间的关联频率,对于可能形成或可能不形成Rb染色体的对来说似乎是相同的。在纯合子Rb 2n = 24的精母细胞中,还由着丝粒异构染色质介导的缔合主要发生在三个端粒二价或八个偏心二价之间。在杂合子Rb 2n = 32的精母细胞中,所有异染色质均位于核外围,但主要观察到三个端粒二价之间以及三价的突触轴之间的缔合。与2n = 40精子细胞中二价相互作用的充分可能性相比,Rb染色体对2n = 24和2n = 32精子细胞的相互作用提出了严格的限制。毫无疑问,Rb染色体的出现改变了2n = 40个精母细胞的祖先核结构,因为它们在染色体结构域之间建立了新类型的相互作用,特别是通过端粒之间的核周边和Rb亚中心的核中心的着丝粒和异色区域。

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