Canonical and noncanonical roles of Hop1 are crucial for meiotic prophase in the fungus Sordaria macrospora.

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences PLoS Biology Pub Date : 2024-07-01 DOI:10.1371/journal.pbio.3002705
Emeline Dubois, Stéphanie Boisnard, Henri-Marc Bourbon, Kenza Yefsah, Karine Budin, Robert Debuchy, Liangran Zhang, Nancy Kleckner, Denise Zickler, Eric Espagne
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Abstract

We show here that in the fungus Sordaria macrospora, the meiosis-specific HORMA-domain protein Hop1 is not essential for the basic early events of chromosome axis development, recombination initiation, or recombination-mediated homolog coalignment/pairing. In striking contrast, Hop1 plays a critical role at the leptotene/zygotene transition which is defined by transition from pairing to synaptonemal complex (SC) formation. During this transition, Hop1 is required for maintenance of normal axis structure, formation of SC from telomere to telomere, and development of recombination foci. These hop1Δ mutant defects are DSB dependent and require Sme4/Zip1-mediated progression of the interhomolog interaction program, potentially via a pre-SC role. The same phenotype occurs not only in hop1Δ but also in absence of the cohesin Rec8 and in spo76-1, a non-null mutant of cohesin-associated Spo76/Pds5. Thus, Hop1 and cohesins collaborate at this crucial step of meiotic prophase. In addition, analysis of 4 non-null mutants that lack this transition defect reveals that Hop1 also plays important roles in modulation of axis length, homolog-axis juxtaposition, interlock resolution, and spreading of the crossover interference signal. Finally, unexpected variations in crossover density point to the existence of effects that both enhance and limit crossover formation. Links to previously described roles of the protein in other organisms are discussed.

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Hop1的规范性和非规范性作用对真菌Sordaria macrospora的减数分裂前期至关重要。
我们在这里发现,在真菌大孢镰刀菌(Sordaria macrospora)中,减数分裂特异性HORMA-domain蛋白Hop1对于染色体轴发育、重组启动或重组介导的同源物联合/配对等基本早期事件并不重要。与此形成鲜明对比的是,Hop1 在从配对到突触复合体(SC)形成的瘦子/紫长子过渡阶段发挥着关键作用。在这一转变过程中,Hop1 需要维持正常的轴结构、形成端粒间的 SC 以及发育重组灶。这些hop1Δ突变体的缺陷依赖于DSB,需要Sme4/Zip1介导的同源体间相互作用程序的进展,可能是通过前SC作用实现的。同样的表型不仅出现在hop1Δ中,也出现在缺乏内聚蛋白Rec8和内聚蛋白相关Spo76/Pds5的非无效突变体spo76-1中。因此,在减数分裂前期的这一关键步骤中,Hop1 和粘合素进行了协作。此外,对缺乏这种过渡缺陷的 4 个非无效突变体的分析表明,Hop1 还在调节轴长度、同源轴并位、连锁分辨率和交叉干扰信号的传播方面发挥着重要作用。最后,交叉密度的意外变化表明,存在着增强和限制交叉形成的效应。研究还讨论了该蛋白在其他生物中的作用。
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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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