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易位携带者精母细胞中的无突触染色质含有组蛋白变体γ-H2AX,并与XY体相关联。

The asynaptic chromatin in spermatocytes of translocation carriers contains the histone variant gamma-H2AX and associates with the XY body.

作者信息

Sciurano R, Rahn M, Rey-Valzacchi G, Solari A J

机构信息

Biologia Celular, CIR, Facultad de Medicina, Universidad de Buenos Aires, Argentina.

出版信息

Hum Reprod. 2007 Jan;22(1):142-50. doi: 10.1093/humrep/del330. Epub 2006 Aug 18.

Abstract

BACKGROUND

The close apposition of multivalents with the XY body has been repeatedly described in heterozygous carriers of chromosomal rearrangements. Because in many of these carriers spermatogenesis is deeply disturbed at the spermatocyte level, the association of autosomal chromatin with the XY body may impair the spermatocyte life.

METHODS

Testicular biopsies from three men carriers of three different chromosomal rearrangements have been analysed by electron microscopy (EM) and immunolocalization of meiotic proteins.

RESULTS

There is an ordered transition from isolated multivalents at early pachytene to XY body association in late pachytene, as shown in a carrier of a rob t(13;14) translocation by EM and in a reciprocal translocation t(9;14) carrier by immunofluorescence. The non-synapsed ends of the quadrivalent show BRCA1 located on the axes and the variant histone gamma-H2AX located on the chromatin. The area covered by gamma-H2AX increases with the association of the asynaptic ends with the XY body in the t(9;14) carrier, and the area covered with gamma-H2AX in the t(Y;15) carrier is larger than that of the XY body of controls.

CONCLUSIONS

The affinity between the inactive XY body and asynaptic regions of multivalents is given a material basis, and transcriptional inactivation is probably shared by these two chromatin types.

摘要

背景

在染色体重排的杂合携带者中,多价体与XY体紧密并置的情况已被多次描述。由于在许多此类携带者中,精子发生在精母细胞水平受到严重干扰,常染色体染色质与XY体的关联可能会损害精母细胞的生命。

方法

对三名携带三种不同染色体重排的男性进行睾丸活检,通过电子显微镜(EM)和减数分裂蛋白的免疫定位进行分析。

结果

如在一名罗伯逊易位t(13;14)携带者中通过EM观察以及在一名相互易位t(9;14)携带者中通过免疫荧光观察所示,从粗线期早期的孤立多价体到粗线期晚期的XY体关联存在有序转变。四价体未联会的末端显示BRCA1位于轴上,而变异组蛋白γ-H2AX位于染色质上。在t(9;14)携带者中,γ-H2AX覆盖的区域随着非联会末端与XY体的关联而增加,并且t(Y;15)携带者中γ-H2AX覆盖的区域大于对照组XY体的区域。

结论

无活性的XY体与多价体的非联会区域之间的亲和力有了物质基础,并且这两种染色质类型可能共享转录失活。

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