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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Male Sterility and Meiotic Drive Associated With Sex Chromosome Rearrangements in Drosophila: Role of X-Y Pairing
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Male Sterility and Meiotic Drive Associated With Sex Chromosome Rearrangements in Drosophila: Role of X-Y Pairing

机译:果蝇性染色体重排相关的雄性不育和减数分裂驱动:X-Y配对的作用

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In Drosophila melanogaster , deletions of the pericentromeric X heterochromatin cause X-Y nondisjunction, reduced male fertility and distorted sperm recovery ratios (meiotic drive) in combination with a normal Y chromosome and interact with Y -autosome translocations ( T(Y;A) ) to cause complete male sterility. The pericentromeric heterochromatin has been shown to contain the male-specific X-Y meiotic pairing sites, which consist mostly of a 240-bp repeated sequence in the intergenic spacers (IGS) of the rDNA repeats. The experiments in this paper address the relationship between X-Y pairing failure and the meiotic drive and sterility effects of Xh deletions. X -linked insertions either of complete rDNA repeats or of rDNA fragments that contain the IGS were found to suppress X-Y nondisjunction and meiotic drive in Xh ?/ Y males, and to restore fertility to Xh ?/ T(Y;A) males for eight of nine tested Y -autosome translocations. rDNA fragments devoid of IGS repeats proved incapable of suppressing either meiotic drive or chromosomal sterility. These results indicate that the various spermatogenic disruptions associated with X heterochromatic deletions are all consequences of X-Y pairing failure. We interpret these findings in terms of a novel model in which misalignment of chromosomes triggers a checkpoint that acts by disabling the spermatids that derive from affected spermatocytes.
机译:在果蝇中,与正常的Y染色体结合使用的着丝粒X异染色质的缺失引起XY不分离,雄性受精率降低和精子恢复率降低(减数分裂驱动),并与Y常染色体易位(T(Y; A))相互作用。男性完全不育。着丝粒异染色质已显示出包含男性特异性X-Y减数分裂配对位点,该位点主要由rDNA重复序列的基因间隔区(IGS)中的240 bp重复序列组成。本文的实验解决了X-Y配对失败与Xh缺失的减数分裂驱动和不育作用之间的关系。发现X链完整rDNA重复序列或包含IGS的rDNA片段的X连锁插入可抑制Xhβ/ Y雄性的XY不分离和减数分裂驱动,并使Xhα/ T(Y; A)雄性恢复八个月的繁殖力。九个测试的Y-常染色体易位。不含IGS重复序列的rDNA片段证明不能抑制减数分裂驱动或染色体不育。这些结果表明,与X异色缺失相关的各种生精破坏都是X-Y配对失败的后果。我们用一个新颖的模型来解释这些发现,在该模型中,染色体的错位会触发一个检查点,该检查点通过禁用源自受影响的精细胞的精细胞而起作用。

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