首页> 美国卫生研究院文献>American Journal of Human Genetics >Cytogenetic analysis of sperm from a man heterozygous for a pericentric inversion inv (3) (p25q21).
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Cytogenetic analysis of sperm from a man heterozygous for a pericentric inversion inv (3) (p25q21).

机译:来自一个杂合子的精子的细胞遗传学分析用于周向反转inv(3)(p25q21)。

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摘要

Human sperm chromosomes were studied in a man heterozygous for a pericentric inversion of chromosome 3(p25q21). The pronuclear chromosomes were analyzed after in vitro penetration of golden hamster eggs. A total of 144 sperm were examined: 69.2% were chromosomally balanced and 30.8% were recombinant. Of the balanced complements, the proportion with a normal chromosome 3 (37.6%) was approximately equal to the proportion with an inverted 3 (31.6%). Of the recombinant complements, the proportion of sperm with a duplication q/deletion p (17.3%) was approximately equal to the reciprocal event of duplication p/deletion q (13.5%). The recombinant chromosome 3 with a duplication q and deletion p has been observed in several abnormal children, but the duplication p/deletion q has never been reported. My results demonstrate that both recombinant chromosomes are produced as expected from an unequal number of crossovers within an inversion loop. In all likelihood the duplication p/deletion q chromosome is an early embryonic lethal because of the amount of genetic material deleted. The proportions of X-bearing (48.9%) and Y-bearing sperm (51.1%) were not significantly different from the expected 1:1 ratio. There was no evidence for an interchromosomal effect. Of the three inversions studied by human sperm chromosome analysis, recombinant chromosomes have been observed only in this case.
机译:在一个人杂合体中研究了人类精子染色体的染色体3(p25q21)的周向反转。在体外金黄仓鼠卵穿透后分析原核染色体。总共检查了144个精子:染色体平衡的精子占69.2%,重组的精子占30.8%。在平衡的补体中,具有正常3号染色体的比例(37.6%)大约等于具有反向3号染色体的比例(31.6%)。在重组补体中,具有重复q /缺失p的精子比例(17.3%)大约等于重复p /缺失q的倒数(13.5%)。在几个异常儿童中观察到了具有重复q和缺失p的重组染色体3,但从未报道重复p /缺失q。我的结果表明,两个重组染色体均产生于反向环内不相等数目的交换所期望的。由于缺失的遗传物质的数量,重复p /缺失q染色体极有可能是早期胚胎致死的。含X精子(48.9%)和含Y精子(51.1%)的比例与预期的1:1比例无显着差异。没有证据表明存在染色体间作用。在人类精子染色体分析研究的三个倒位中,只有在这种情况下才观察到重组染色体。

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