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蛋白酶体激活剂PA200是正常精子发生所必需的。

Proteasome activator PA200 is required for normal spermatogenesis.

作者信息

Khor Bernard, Bredemeyer Andrea L, Huang Ching-Yu, Turnbull Isaiah R, Evans Ryan, Maggi Leonard B, White J Michael, Walker Laura M, Carnes Kay, Hess Rex A, Sleckman Barry P

机构信息

Department of Pathology and Immunology, Campus Box 8118, Washington University School of Medicine, 660 S. Euclid Ave., St. Louis, MO 63110, USA.

出版信息

Mol Cell Biol. 2006 Apr;26(8):2999-3007. doi: 10.1128/MCB.26.8.2999-3007.2006.

Abstract

The PA200 proteasome activator is a broadly expressed nuclear protein. Although how PA200 normally functions is not fully understood, it has been suggested to be involved in the repair of DNA double-strand breaks (DSBs). The PA200 gene (Psme4) is composed of 45 coding exons spanning 108 kb on mouse chromosome 11. We generated a PA200 null allele (PA200(Delta)) through Cre-loxP-mediated interchromosomal recombination after targeting loxP sites at either end of the locus. PA200(Delta/Delta) mice are viable and have no obvious developmental abnormalities. Both lymphocyte development and immunoglobulin class switching, which rely on the generation and repair of DNA DSBs, are unperturbed in PA200(Delta/Delta) mice. Additionally, PA200(Delta/Delta) embryonic stem cells do not exhibit increased sensitivity to either ionizing radiation or bleomycin. Thus, PA200 is not essential for the repair of DNA DSBs generated in these settings. Notably, loss of PA200 led to a marked reduction in male, but not female, fertility. This was due to defects in spermatogenesis observed in meiotic spermatocytes and during the maturation of postmeiotic haploid spermatids. Thus, PA200 serves an important nonredundant function during spermatogenesis, suggesting that the efficient generation of male gametes has distinct protein metabolic requirements.

摘要

PA200蛋白酶体激活剂是一种广泛表达的核蛋白。尽管PA200的正常功能尚未完全了解,但有人认为它参与DNA双链断裂(DSB)的修复。PA200基因(Psme4)由45个编码外显子组成,跨越小鼠11号染色体上的108 kb。我们通过在该基因座两端靶向loxP位点后,利用Cre-loxP介导的染色体间重组产生了一个PA200无效等位基因(PA200(Delta))。PA200(Delta/Delta)小鼠是存活的,没有明显的发育异常。依赖于DNA DSB产生和修复的淋巴细胞发育和免疫球蛋白类别转换在PA200(Delta/Delta)小鼠中均未受到干扰。此外,PA200(Delta/Delta)胚胎干细胞对电离辐射或博来霉素均未表现出增加的敏感性。因此,PA200对于这些情况下产生的DNA DSB的修复不是必需的。值得注意的是,PA200的缺失导致雄性而非雌性生育力显著降低。这是由于在减数分裂的精母细胞和减数分裂后单倍体精子细胞成熟过程中观察到的精子发生缺陷。因此,PA200在精子发生过程中发挥重要的非冗余功能,这表明雄性配子的有效产生具有独特的蛋白质代谢需求。

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