The chromatin-associated 53BP1 ortholog, HSR-9, regulates recombinational repair and X chromosome segregation in the Caenorhabditis elegans germ line.

IF 3.3 3区 生物学 Q2 GENETICS & HEREDITY Genetics Pub Date : 2024-08-07 DOI:10.1093/genetics/iyae102
Qianyan Li, Sara Hariri, Aashna Calidas, Arshdeep Kaur, Erica Huey, JoAnne Engebrecht
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Abstract

53BP1 plays a crucial role in regulating DNA damage repair pathway choice and checkpoint signaling in somatic cells; however, its role in meiosis has remained enigmatic. In this study, we demonstrate that the Caenorhabditis elegans ortholog of 53BP1, HSR-9, associates with chromatin in both proliferating and meiotic germ cells. Notably, HSR-9 is enriched on the X chromosome pair in pachytene oogenic germ cells. HSR-9 is also present at kinetochores during both mitotic and meiotic divisions but does not appear to be essential for monitoring microtubule-kinetochore attachments or tension. Using cytological markers of different steps in recombinational repair, we found that HSR-9 influences the processing of a subset of meiotic double-stranded breaks into COSA-1-marked crossovers. Additionally, HSR-9 plays a role in meiotic X chromosome segregation under conditions where X chromosomes fail to pair, synapse, and recombine. Together, these results highlight that chromatin-associated HSR-9 has both conserved and unique functions in the regulation of meiotic chromosome behavior.

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染色质相关 53BP1 同源物 HSR-9 在秀丽隐杆线虫种系中调控重组修复和 X 染色体分离。
53BP1 在调节体细胞中 DNA 损伤修复途径选择和检查点信号转导方面起着至关重要的作用;然而,它在减数分裂中的作用却一直是个谜。在这项研究中,我们证明了草履虫 53BP1 的直向同源物 HSR-9 在增殖和减数分裂生殖细胞中都与染色质结合。值得注意的是,HSR-9富集在青春期卵原生殖细胞的X染色体对上。在有丝分裂和减数分裂过程中,HSR-9 也存在于着丝点上,但似乎对监测微管-着丝点的附着或张力并不重要。我们利用重组修复不同步骤的细胞学标记发现,HSR-9 会影响减数分裂双股断裂子集转化为 COSA-1 标记交叉的过程。此外,在 X 染色体不能配对、突触和重组的条件下,HSR-9 在减数分裂 X 染色体分离中发挥作用。这些结果突出表明,染色质相关的 HSR-9 在调控减数分裂染色体行为方面既有保守的功能,也有独特的功能。
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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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