Forejt J, Gregorová S, Goetz P
Chromosoma. 1981;82(1):41-53. doi: 10.1007/BF00285748.
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.
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。