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缺乏多泛素基因 Ubb 的小鼠睾丸基因表达模式的改变。

Altered testicular gene expression patterns in mice lacking the polyubiquitin gene Ubb.

机构信息

Bio-X Program, Department of Biology, Stanford University, Stanford, California 94305, USA.

出版信息

Mol Reprod Dev. 2011 Jun;78(6):415-25. doi: 10.1002/mrd.21318. Epub 2011 May 3.

Abstract

Ubiquitin (Ub) is an essential protein found in all eukaryotic cells and plays important roles in a variety of cellular functions including germ cell development. We have previously reported that targeted disruption of the polyubiquitin gene Ubb results in male and female infertility in Ubb(-/-) mice, with germ cells arrested at meiotic prophase I. Although reduced Ub levels in germ cells are believed to be responsible for the fertility defect in Ubb(-/-) mice, it is still unclear how reduced Ub levels result in sterility. Here we describe the results of a microarray analysis of the murine testicular transcriptome, which demonstrates dramatically altered gene expression patterns in Ubb(-/-) mice, possibly related to reduced levels of histone 2A (H2A) ubiquitylation. We find that large numbers of genes related to fertility, metabolism, transcription, and the ubiquitin-proteasome system (UPS) are misregulated in Ubb(-/-) mice. Such wide-ranging alterations in gene expression suggest that loss of the Ubb gene does not mimic a single-gene defect phenotype, but instead may affect gene expression more globally. These dramatic changes in gene expression could, at least in part, contribute to the complex fertility and metabolic phenotypes seen in these mice.

摘要

泛素(Ub)是一种存在于所有真核细胞中的必需蛋白,在包括生殖细胞发育在内的多种细胞功能中发挥着重要作用。我们之前曾报道过,靶向敲除多泛素基因 Ubb 会导致 Ubb(-/-) 小鼠的雄性和雌性不育,生殖细胞停滞在减数分裂前期 I。尽管生殖细胞中泛素水平的降低被认为是导致 Ubb(-/-) 小鼠生育缺陷的原因,但仍不清楚泛素水平的降低如何导致不育。在这里,我们描述了对 Ubb(-/-) 小鼠睾丸转录组的微阵列分析结果,该分析表明 Ubb(-/-) 小鼠的基因表达模式发生了显著改变,这可能与组蛋白 2A(H2A)泛素化水平降低有关。我们发现,大量与生育、代谢、转录和泛素-蛋白酶体系统(UPS)相关的基因在 Ubb(-/-) 小鼠中失调。这种广泛的基因表达改变表明,Ubb 基因的缺失并不模拟单一基因缺陷表型,而是可能更广泛地影响基因表达。这些基因表达的巨大变化至少在一定程度上导致了这些小鼠中复杂的生育和代谢表型。

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