pp1 γ - 1不能替代哺乳动物特有的pp1 γ - 2异构体来支持雄性生育能力和精子功能。

IF 3.7 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Reproduction Pub Date : 2025-01-21 Print Date: 2025-02-01 DOI:10.1530/REP-24-0256
Souvik Dey, Wesam Nofal, Cameron Brothag, Mustfa Kabi, Aditi Khamamkar, Neha Choudhari, Srinivasan Vijayaraghavan
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引用次数: 0

摘要

丝氨酸-苏氨酸磷酸酶有PP1α、PP1β、PP1γ1和PP1γ2 4个类似物,由Ppp1ca、Ppp1cb和Ppp1cc 3个基因编码。蛋白磷酸酶PP1γ2是Ppp1cc基因的两种亚型之一,在睾丸和精子的生精细胞中表达,而PP1γ1在体细胞中发现。这两种PP1γ同工异构体是由交替剪接形成的,这种剪接只发生在哺乳动物中,除了它们的c端外,它们是相同的。在小鼠中,Ppp1cc的整体或睾丸敲除会导致精子和中后期精子发生中断,从而导致男性不育。在睾丸特异性启动子的驱动下,pp1γ - 2的转基因表达在分化的生精细胞中,挽救了pp1cc缺失小鼠的精子发生和生育能力。为什么pp1 γ - 2是必需的,而且只存在于哺乳动物的精子中,这是一个谜。我们已经产生了敲入小鼠,其中Ppp1cc基因被编辑为仅表达PP1γ1。敲入小鼠精子发生正常。敲入小鼠睾丸中表达的pp1 γ - 1和野生型小鼠睾丸中表达的pp1 γ - 2均以等量掺入精子中。含有pp1 γ - 1的精子使鞭毛跳动幅度和活力降低,雄性小鼠的生殖力严重不足。虽然在野生型小鼠中,pp1 γ - 2在头部和尾部都存在,但在敲入型小鼠中,pp1 γ - 1在精子头部缺失,导致精子内蛋白磷酸酶景观发生改变。精子蛋白的磷酸化蛋白质组学分析表明PP1γ - 1功能受损的一个合理的分子基础:它确定了PP1的已知底物GSK3α在敲入精子中失调。本研究初步解释了pp1 γ - 2对男性生育能力的异构体特异性需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PP1γ1 is unable to substitute for the mammal-specific PP1γ2 isoform to support male fertility and sperm function.

In brief: Protein phosphatase 1 catalytic subunit gamma isoform 2 (PP1γ2) is a unique phosphatase expressed only in mammalian testes and sperm cells. The PP1γ2 isoform is indispensable for sperm motility and fertility and cannot be replaced by the PP1γ1 isoform for these functions.

Abstract: The serine-threonine phosphatase has four paralogs - PP1α, PP1β, PP1γ1 and PP1γ2 - encoded by three genes, Ppp1ca, Ppp1cb and Ppp1cc. Protein phosphatase PP1γ2, one of two isoforms of the gene Ppp1cc, is expressed in spermatogenic cells in the testes and sperm, while PP1γ1 is found in somatic cells. The two PP1γ isoforms, formed by alternate splicing that occurs only in mammals, are identical except at their C-termini. Global or testis-specific knockout of Ppp1cc in mice results in male infertility due to disrupted spermiation and mid-to-late spermiogenesis. Transgenic expression of PP1γ2, driven by a testis-specific promoter in differentiating spermatogenic cells, rescues spermatogenesis and fertility in the Ppp1cc-null mice. Why PP1γ2 is essential and present only in mammalian sperm is a mystery. We have generated a knock-in mouse where the Ppp1cc gene is edited to express only PP1γ1. Spermatogenesis was normal in knock-in mice. Testis-expressed PP1γ1 in the knock-in mice and PP1γ2 in the wild-type mice were incorporated in equal amounts into sperm. Sperm bearing PP1γ1 have reduced flagellar beat amplitude and motility, and male mice were severely sub-fertile. Although in the wild-type mice, PP1γ2 is present in both the head and tail, in the knock-in mice, PP1γ1 is absent in sperm heads, leading to an altered intra-sperm protein phosphatase landscape. Phosphoproteomic analysis of sperm proteins suggested a plausible molecular basis for compromised PP1γ1 functions: it identified GSK3α, a known substrate of PP1, to be dysregulated in knock-in sperm. This study provides a preliminary explanation for the isoform-specific requirement of PP1γ2 for male fertility.

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来源期刊
Reproduction
Reproduction 生物-发育生物学
CiteScore
7.40
自引率
2.60%
发文量
199
审稿时长
4-8 weeks
期刊介绍: Reproduction is the official journal of the Society of Reproduction and Fertility (SRF). It was formed in 2001 when the Society merged its two journals, the Journal of Reproduction and Fertility and Reviews of Reproduction. Reproduction publishes original research articles and topical reviews on the subject of reproductive and developmental biology, and reproductive medicine. The journal will consider publication of high-quality meta-analyses; these should be submitted to the research papers category. The journal considers studies in humans and all animal species, and will publish clinical studies if they advance our understanding of the underlying causes and/or mechanisms of disease. Scientific excellence and broad interest to our readership are the most important criteria during the peer review process. The journal publishes articles that make a clear advance in the field, whether of mechanistic, descriptive or technical focus. Articles that substantiate new or controversial reports are welcomed if they are noteworthy and advance the field. Topics include, but are not limited to, reproductive immunology, reproductive toxicology, stem cells, environmental effects on reproductive potential and health (eg obesity), extracellular vesicles, fertility preservation and epigenetic effects on reproductive and developmental processes.
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