Poldip2 promotes mtDNA elimination during Drosophila spermatogenesis to ensure maternal inheritance.

IF 8.3 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY EMBO Journal Pub Date : 2025-03-01 Epub Date: 2025-02-11 DOI:10.1038/s44318-025-00378-4
Ziming Wang, Tirawit Meerod, Nuria Cortes-Silva, Ason C-Y Chiang, Ziyan Nie, Ying Di, Peiqiang Mu, Ankit Verma, Adam James Reid, Hansong Ma
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Abstract

Maternal inheritance of mitochondrial DNA (mtDNA) is highly conserved in metazoans. While many species eliminate paternal mtDNA during late sperm development to foster maternal inheritance, the regulatory mechanisms governing this process remain elusive. Through a forward genetic screen in Drosophila, we identified 47 mutant lines exhibiting substantial retention of mtDNA in mature sperm. We mapped one line to poldip2, a gene predominantly expressed in the testis. Disruption of poldip2 led to substantial mtDNA retention in mature sperm and subsequent paternal transmission to progeny. Further investigation via imaging, biochemical analyses and ChIP assays revealed that Poldip2 is a mitochondrial matrix protein capable of binding mtDNA. Moreover, we showed that ClpX, the key component of a major mitochondrial protease, interacts with Poldip2 to co-regulate mtDNA elimination in Drosophila spermatids. This study sheds light on the mechanisms underlying mtDNA removal during spermatogenesis and underscores the pivotal role of this process in safeguarding maternal inheritance.

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在果蝇精子发生过程中,Poldip2促进mtDNA的消除,以确保母体遗传。
线粒体DNA (mtDNA)的母系遗传在后生动物中高度保守。虽然许多物种在精子发育后期消除父系mtDNA以促进母系遗传,但控制这一过程的调节机制仍然难以捉摸。通过对果蝇的前向遗传筛选,我们发现47个突变系在成熟精子中表现出mtDNA的大量保留。我们将其中一条线定位到poldip2,这是一种在睾丸中主要表达的基因。poldip2的破坏导致成熟精子中大量的mtDNA保留和随后的父系遗传给后代。通过成像、生化分析和ChIP分析进一步研究表明,Poldip2是一种能够结合mtDNA的线粒体基质蛋白。此外,我们发现ClpX是一种主要线粒体蛋白酶的关键成分,它与Poldip2相互作用,共同调节果蝇精子中mtDNA的消除。这项研究揭示了精子发生过程中mtDNA去除的机制,并强调了这一过程在保护母体遗传中的关键作用。
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来源期刊
EMBO Journal
EMBO Journal 生物-生化与分子生物学
CiteScore
18.90
自引率
0.90%
发文量
246
审稿时长
1.5 months
期刊介绍: The EMBO Journal has stood as EMBO's flagship publication since its inception in 1982. Renowned for its international reputation in quality and originality, the journal spans all facets of molecular biology. It serves as a platform for papers elucidating original research of broad general interest in molecular and cell biology, with a distinct focus on molecular mechanisms and physiological relevance. With a commitment to promoting articles reporting novel findings of broad biological significance, The EMBO Journal stands as a key contributor to advancing the field of molecular biology.
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