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X-常染色体易位携带者公牛的性染色体组成与精子头部畸形的突触模式

Synaptic pattern of sex complements and sperm head malformation in X-autosome translocation carrier bulls.

作者信息

Basrur P K, Koykul W, Baguma-Nibasheka M, King W A, Ambady S, Ponce de León F A

机构信息

Department of Biomedical Sciences, Ontario Veterinary College, University of Guelph, Guelph, Ontario, Canada.

出版信息

Mol Reprod Dev. 2001 May;59(1):67-77. doi: 10.1002/mrd.1008.

Abstract

Testicular activity and semen characteristics of bulls carrying an X-autosome translocation t(Xp +;23q-) revealed all stages of spermatogenesis although their semen consisted of few and, exclusively, of malformed spermatozoa. Chromosome painting on metaphase spreads of their mother and synaptonemal complex analysis on these and normal bulls were carried out to test whether the location and meiotic pairing behaviour of the rearranged segments could have contributed to the sperm head malformation and oligospermia in our X-autosome translocation (X-AT) carrier bulls. Spermatocytes of X-AT carriers displayed the rearranged chromosomes in a univalent-trivalent association, with 23q- always remaining as a univalent and Xp + in synapsis with normal chromosome 23 and the Y chromosome. Chromosome painting studies to test whether the total absence of meiocytes showing a quadrivalent is due to the non-reciprocal nature of this translocation, identified Xp sequence homology with the distal end of 23q- confirming its relocation to the terminal segment of 23q-. Our synaptonemal complex analyses also confirmed that the bovine pseudo-autosomal region (PAR) is at the distal ends of Xq and Yp and further revealed that over 85% of spermatocytes of X-AT carriers (and up to 13% of spermatocytes of normal bulls) sustain a Y-axis break adjacent to the PAR. Although the exact cause of a Y-axis break in bovine spermatocytes is not known at present, we believe that the break and possible loss of Yq in such high proportions of spermatocytes of X-AT carriers could have contributed to the sperm head malformation and oligospermia in our X-AT carrier bulls.

摘要

携带X-常染色体易位t(Xp +;23q-)的公牛的睾丸活动和精液特征显示了精子发生的各个阶段,尽管它们的精液中精子数量很少,且全部为畸形精子。对其母亲的中期染色体铺展进行染色体描绘,并对这些公牛和正常公牛进行联会复合体分析,以测试重排片段的位置和减数分裂配对行为是否可能导致了我们的X-常染色体易位(X-AT)携带者公牛的精子头部畸形和少精子症。X-AT携带者的精母细胞以单价-三价联合体形式显示重排染色体,23q-始终保持为单价,而Xp +与正常的23号染色体和Y染色体联会。通过染色体描绘研究来测试是否由于这种易位的非相互性质导致完全没有显示四价的减数分裂细胞,结果确定Xp序列与23q-的远端具有同源性,证实其重新定位到23q-的末端片段。我们的联会复合体分析还证实,牛的假常染色体区域(PAR)位于Xq和Yp的远端,并进一步揭示,X-AT携带者超过85%的精母细胞(正常公牛的精母细胞中高达13%)在PAR附近发生Y轴断裂。尽管目前尚不清楚牛精母细胞中Y轴断裂的确切原因,但我们认为,在如此高比例的X-AT携带者精母细胞中Yq的断裂和可能的丢失可能导致了我们的X-AT携带者公牛的精子头部畸形和少精子症。

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