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组蛋白巨H2A1.2在精子发生的粗线期早期集中于XY小体。

Histone macroH2A1.2 is concentrated in the XY-body by the early pachytene stage of spermatogenesis.

作者信息

Hoyer-Fender S, Costanzi C, Pehrson J R

机构信息

Universität Göttingen, III, Zoologisches Institut-Entwicklungsbiologie, Humboldtallee 34A, Göttingen, 37073, Germany.

出版信息

Exp Cell Res. 2000 Aug 1;258(2):254-60. doi: 10.1006/excr.2000.4951.

Abstract

The pairing of sex chromosomes during meiosis in male mammals is associated with ongoing heterochromatinization and X inactivation. This process occurs in a specific area of the nucleus that can be discerned morphologically: the sex vesicle or XY-body. In contrast to X inactivation in the somatic cells of female mammals the reasons for X inactivation in the male germline remain obscure. We have recently demonstrated that the inactive X chromosome in somatic cells of female mammals is marked by a high concentration of histone macroH2A. Here we investigate X inactivation in the meiotic cells of the male germline. We demonstrate here that macroH2A1.2 is present in the nuclei of germ cells starting first with localization that is largely, if not exclusively, to the developing XY-body in early pachytene spermatocytes. Our results suggest that inactivation of sex chromosomes in the male germ cell includes a major alteration of the nucleosomal structure.

摘要

在雄性哺乳动物减数分裂过程中,性染色体的配对与持续的异染色质化和X染色体失活有关。这一过程发生在细胞核的一个特定区域,该区域在形态上可被识别:性泡或XY体。与雌性哺乳动物体细胞中的X染色体失活不同,雄性生殖系中X染色体失活的原因仍不清楚。我们最近证明,雌性哺乳动物体细胞中的失活X染色体以高浓度的组蛋白macroH2A为特征。在这里,我们研究雄性生殖系减数分裂细胞中的X染色体失活。我们在此证明,macroH2A1.2存在于生殖细胞的细胞核中,最初主要定位于早粗线期精母细胞中正在发育的XY体,即便不是完全定位于此。我们的结果表明,雄性生殖细胞中性染色体的失活包括核小体结构的重大改变。

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