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鉴定一个新的编码 SYCP3 样蛋白的小鼠基因,该蛋白在雄性减数分裂 I 的前期从 XY 体重新定位到核仁。

Characterization of a novel mouse gene encoding an SYCP3-like protein that relocalizes from the XY body to the nucleolus during prophase of male meiosis I.

机构信息

Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.

出版信息

Biol Reprod. 2011 Jul;85(1):165-71. doi: 10.1095/biolreprod.110.087270. Epub 2011 Mar 30.

Abstract

Xlr6 is a novel but uncharacterized X-linked gene that is upregulated in meiotic prophase I during mouse spermatogenesis. Xlr6 belongs to the Xlr gene family, which includes a component of the axial/lateral element of the synaptonemal complex, Sycp3, and its transcripts are abundant in the fetal ovary and adult testis. Immunostaining and Western blot analysis demonstrate a diffuse localization pattern for this protein in the nucleus and an association with chromatin during the leptotene and zygotene stages. In males, XLR6 accumulates at the XY body of early pachytene to midpachytene spermatocytes, although the Xlr6 gene is subjected to meiotic sex chromosome inactivation. During the late pachytene and diplotene stages, the XLR6 protein relocalizes from the XY body to the nucleolus and, eventually, disappears by diakinesis. In females, XLR6 disappears at the pachytene stage, whereas it accumulates at the unpaired chromosomes occasionally observed in wild-type female mice. Although the amino acid sequence of XLR6 has a high similarity with SYCP3, its distinct localization pattern and dynamism suggest a unique chromatin modification function that leads to the transcriptional repression of ribosomal DNA in addition to sex chromosome genes.

摘要

Xlr6 是一个新的但尚未确定功能的 X 连锁基因,在小鼠精子发生的减数分裂前期 I 中上调。Xlr6 属于 Xlr 基因家族,该家族包括联会复合体的轴/侧元件的一个组成部分,Sycp3,其转录本在胎儿卵巢和成年睾丸中丰富表达。免疫染色和 Western blot 分析表明,该蛋白在细胞核中呈现弥散定位模式,并在细线期和偶线期与染色质相关联。在雄性中,XLR6 在早期粗线期到中期粗线期精母细胞的 XY 体上积累,尽管 Xlr6 基因受到减数分裂性染色体失活的影响。在晚期粗线期和双线期,XLR6 蛋白从 XY 体重新定位到核仁,最终在减数分裂前期消失。在雌性中,XLR6 在粗线期消失,而在野生型雌性小鼠中偶尔观察到的未配对染色体上积累。尽管 XLR6 的氨基酸序列与 SYCP3 具有高度相似性,但它独特的定位模式和动态性表明其具有独特的染色质修饰功能,除了性别染色体基因外,还能导致核糖体 DNA 的转录抑制。

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