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鉴定和表达哺乳动物有丝分裂到减数分裂过渡的潜在调节因子。

Identification and expression of potential regulators of the mammalian mitotic-to-meiotic transition.

机构信息

School of Molecular Biosciences and The Center for Reproductive Biology, Washington State University, Pullman, Washington 99164, USA.

出版信息

Biol Reprod. 2011 Jan;84(1):34-42. doi: 10.1095/biolreprod.110.086215. Epub 2010 Sep 8.

Abstract

Meiosis is unique to germ cells and occurs in a sex-specific manner. The genes regulating meiotic initiation in either sex are yet to be fully elucidated. Recent studies have revealed the importance of retinoic acid and one of its target genes, Stra8, in meiotic initiation in both sexes. Microarray analysis of whole murine embryonic ovary and postnatal testis time course data revealed a single peak of Stra8 expression in each organ at the onset of meiosis; at Embryonic Day 14.5 in the ovary and 10 days postpartum in the testis. In order to identify other genes involved in the initiation of meiosis in mammals, murine testis and ovary microarray data were examined more closely for transcripts with expression profiles similar to Stra8. Three such candidates include establishment of cohesion 1 homolog 2 (Esco2), encoding a protein essential for sister chromatid cohesion; SET domain, bifurcated 2 (Setdb2), the mouse ortholog of Eggless, which is essential for oogenesis in Drosophila; and ubiquitin-activating enzyme 6 (Uba6), a gene with fivefold higher expression in human and mouse testes than any other organ. In situ hybridization and immunohistochemistry or immunofluorescence were performed to localize Esco2, Setbd2, and Uba6 expression in the developing testis. The cellular expression pattern localized all three of these transcripts and their respective proteins to germ cells transitioning from mitosis to meiosis, hence supporting the hypothesis of their involvement in the initiation of meiosis. Future research will be directed at determining a specific role for these three proteins in germ cell differentiation.

摘要

减数分裂是生殖细胞所特有的,并且以性别特异性的方式发生。调节任性别减数分裂起始的基因尚未完全阐明。最近的研究揭示了视黄酸及其靶基因 Stra8 在两性减数分裂起始中的重要性。对整个小鼠胚胎卵巢和出生后睾丸时间过程数据的微阵列分析显示,在每个器官的减数分裂起始时,Stra8 表达都有一个单一的高峰;在卵巢中为胚胎第 14.5 天,在睾丸中为产后 10 天。为了鉴定哺乳动物减数分裂起始中涉及的其他基因,对小鼠睾丸和卵巢微阵列数据进行了更仔细的检查,以寻找与 Stra8 表达谱相似的转录本。有三个这样的候选者,包括着丝粒凝聚 1 同源物 2(Esco2),编码对于姐妹染色单体凝聚必不可少的蛋白质;SET 结构域,分叉 2(Setdb2),Eggless 的小鼠同源物,对于果蝇的卵子发生是必不可少的;和泛素激活酶 6(Uba6),在人类和小鼠睾丸中的表达比任何其他器官高五倍。进行了原位杂交和免疫组织化学或免疫荧光,以定位 Esco2、Setbd2 和 Uba6 在发育中的睾丸中的表达。这些转录本及其各自的蛋白质的细胞表达模式都定位于从有丝分裂向减数分裂过渡的生殖细胞,从而支持它们参与减数分裂起始的假说。未来的研究将致力于确定这三种蛋白质在生殖细胞分化中的特定作用。

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