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XY 配对与小鼠(小家鼠)粗线期精母细胞中常染色体雄性不育易位的联会复合体相关。

XY pair associates with the synaptonemal complex of autosomal male-sterile translocations in pachytene spermatocytes of the mouse (Mus musculus).

作者信息

Forejt J, Gregorová S, Goetz P

出版信息

Chromosoma. 1981;82(1):41-53. doi: 10.1007/BF00285748.

DOI:10.1007/BF00285748
PMID:6167408
Abstract

Analysis of the chromosome behaviour at pachytene has been performed by means of the silver staining technique visualizing the synaptonemal complexes (SCs) in male mice heterozygous for the male-sterile translocations T(5;12)31Hm T(16;17)43H and T(7;19)145H, respectively. the T(9;17)138Ca male heterozygotes and T43H/T43H homozygous males were used as fertile controls. The sterile mice displayed a high frequency (about 60%) of pachytene spermatocytes with autosomal translocation configuration located in close vicinity of the XY pair. The dense round body (XAB), normally located near the X-chromosome axis in fertile males, exhibited abnormal affinity to translocation configuration in the sterile translocation heterozygotes. The incomplete synapsis of autosomes involved in translocation configuration was observed in more than 70% of the pachytene spermatocytes with the male-sterile translocations but less than 20% of the cells from T138Ca fertile male.s. A hypothesis relating the spermatogenic arrest of carriers of male-sterile rearrangements to the presumed interference with X chromosome inactivation in male meiosis is discussed.

摘要

利用银染技术对粗线期染色体行为进行了分析,该技术可使分别携带雄性不育易位T(5;12)31Hm、T(16;17)43H和T(7;19)145H的雄性小鼠中的联会复合体(SCs)可视化。以T(9;17)138Ca雄性杂合子和T43H/T43H纯合雄性作为可育对照。不育小鼠中,粗线期精母细胞出现常染色体易位构型且位于XY对附近的频率很高(约60%)。在可育雄性中通常位于X染色体轴附近的致密圆体(XAB),在不育易位杂合子中对易位构型表现出异常亲和力。在超过70%携带雄性不育易位的粗线期精母细胞中观察到参与易位构型的常染色体不完全联会,但来自T138Ca可育雄性的细胞中这一比例不到20%。本文讨论了一个假说,即雄性不育重排携带者的生精停滞与雄性减数分裂中对X染色体失活的假定干扰有关。

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1
XY pair associates with the synaptonemal complex of autosomal male-sterile translocations in pachytene spermatocytes of the mouse (Mus musculus).XY 配对与小鼠(小家鼠)粗线期精母细胞中常染色体雄性不育易位的联会复合体相关。
Chromosoma. 1981;82(1):41-53. doi: 10.1007/BF00285748.
2
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本文引用的文献

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A reciprocal translocation induced in an oocyte and affecting fertility in male mice.在卵母细胞中诱导产生的一种相互易位,影响雄性小鼠的生育能力。
Cytogenet Cell Genet. 1980;27(2-3):129-46. doi: 10.1159/000131474.
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Genetically enhanced asynapsis of autosomal chromatin promotes transcriptional dysregulation and meiotic failure.常染色体染色质的基因增强型联会消失会促进转录失调和减数分裂失败。
Chromosoma. 2012 Feb;121(1):91-104. doi: 10.1007/s00412-011-0346-5. Epub 2011 Oct 16.
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Complex meiotic configuration of the holocentric chromosomes: the intriguing case of the scorpion Tityus bahiensis.着丝粒染色体的复杂减数分裂构型:蝎子 Tityus bahiensis 的有趣案例。
Chromosome Res. 2009;17(7):883-98. doi: 10.1007/s10577-009-9076-4. Epub 2009 Sep 4.
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Evolution of multiple sex chromosomes in the spider genus Malthonica (Araneae: Agelenidae) indicates unique structure of the spider sex chromosome systems.马尔托尼亚蛛属(蜘蛛目:漏斗蛛科)中多条性染色体的演化表明蜘蛛性染色体系统具有独特结构。
Chromosome Res. 2007;15(7):863-79. doi: 10.1007/s10577-007-1169-3. Epub 2007 Oct 1.
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Genome Res. 2007 Oct;17(10):1431-7. doi: 10.1101/gr.6520107. Epub 2007 Aug 23.
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Autosomal translocations causing male sterility and viable aneuploidy in the mouse.导致小鼠雄性不育和存活非整倍体的常染色体易位。
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The spatial relationship of the X and Y chromosomes during meiotic prophase in mouse spermatocytes.小鼠精母细胞减数分裂前期X和Y染色体的空间关系。
Chromosoma. 1970;29(2):217-36. doi: 10.1007/BF00326080.
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Translocations, the predominant cause of total sterility in sons of mice treated with mutagens.易位是用诱变剂处理过的小鼠雄性后代完全不育的主要原因。
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