Chandley A C, McBeath S, Speed R M, Yorston L, Hargreave T B
J Med Genet. 1987 Jun;24(6):325-34. doi: 10.1136/jmg.24.6.325.
A pericentric inversion in chromosome 1 of a severely oligospermic human male is reported. Pachytene analysis in microspread preparations shows an absence of full loop formation in the inversion bivalent and only the rare occurrence of a partial loop. The majority of cells exhibit extensive asynapsis across the inverted segment, or a normal looking synaptonemal complex indicative of heterologous pairing along the length of the inversion. Crossing over is reduced in the No 1 bivalent with only a rare chiasma being seen in the inverted region at metaphase I. Males heterozygous for a pericentric inversion in chromosome 1 appear to be at severe risk for infertility brought about by spermatogenic disturbance. The dearth of full loops at prophase in this patient, and in other pericentric inversion cases studied both in man and other species, raises the question of whether recombinant offspring might be rarer than anticipated on a theoretical basis owing to asynapsis or early heterologous synapsis across inverted segments.
报道了一名严重少精子症男性患者1号染色体的臂间倒位情况。对微铺展制片进行粗线期分析显示,倒位二价体中未形成完整的环,仅偶尔出现部分环。大多数细胞在倒位区段表现出广泛的联会消失,或出现外观正常的联会复合体,表明在倒位区段全长存在异源配对。1号二价体的交叉互换减少,在中期I的倒位区域仅偶尔可见交叉。1号染色体臂间倒位的杂合男性似乎因生精障碍而面临严重的不育风险。该患者以及在人类和其他物种中研究的其他臂间倒位病例在前期缺乏完整的环,这就提出了一个问题,即由于倒位区段的联会消失或早期异源联会,重组后代是否可能比理论预期的更罕见。