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对一名患有1号染色体臂间倒位inv(1)(p32q42)的不育男性携带者的联会复合体进行电子显微镜研究。发现有规则的环形成,但联会存在缺陷,包括可能的染色体间效应。

Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1)(p32q42). Regular loop formation but defective synapsis including a possible interchromosomal effect.

作者信息

Batanian J, Hulten M A

出版信息

Hum Genet. 1987 May;76(1):81-9. doi: 10.1007/BF00283055.

Abstract

Electron microscopic investigations of surface spread synaptonemal complexes in spermatocytes from a 37-year-old man ascertained for infertility detected a pericentric inv(1), and subsequent lymphocyte analysis placed the breakpoints at p32 and q42. Most spermatocytes showed a maturation arrest at mid-pachytene explaining the azoospermia. As in two other comparatively large loop-forming pericentric inversions, initiation of synapsis took place in the middle of the inverted segment. Thus there is no indication of interstitial synaptic initiation being restricted to special pairing sites along the length of the chromosome. All spermatocytes investigated at mid-pachytene showed inversion loops, none of which was fully synapsed with a specific delay in pairing of the heterochromatic block 1qh and adjacent segments. The loops were of similar size in all the cells examined and synaptic adjustment had not taken place. There was no indication of a preferential association between the inv(1) bivalent and the XY configuration, and a functional disturbance of the X seems an unlikely reason for the meiotic maturation arrest. The most likely cause may be the failure of adequate synapsis of the inverted segment and the possibly associated pairing abnormalities of other homologues, including asynapsis and/or precocious desynapsis.

摘要

对一名因不育症接受检查的37岁男性精子细胞中表面伸展的联会复合体进行电子显微镜研究,发现了一个近着丝粒倒位inv(1),随后的淋巴细胞分析确定断点位于p32和q42。大多数精子细胞在粗线期中期出现成熟停滞,这解释了无精子症的原因。与其他两个相对较大的形成环的近着丝粒倒位一样,联会起始发生在倒位片段的中间。因此,没有迹象表明间期联会起始仅限于染色体长度上的特殊配对位点。在粗线期中期研究的所有精子细胞都显示出倒位环,其中没有一个与异染色质块1qh和相邻片段的配对有特定延迟而完全联会。在所检查的所有细胞中,环的大小相似,并且没有发生联会调整。没有迹象表明inv(1)二价体与XY构型之间存在优先关联,并且X染色体的功能紊乱似乎不太可能是减数分裂成熟停滞的原因。最可能的原因可能是倒位片段的充分联会失败以及其他同源染色体可能相关的配对异常,包括联会失败和/或过早解联会。

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