ISWI1复合蛋白促进了鹦鹉螺的发育基因组编辑

IF 6.2 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Genome research Pub Date : 2024-11-14 DOI:10.1101/gr.278402.123
Aditi Singh, Lilia Häußermann, Christiane Emmerich, Emily Nischwitz, Brandon KB Seah, Falk Butter, Mariusz Nowacki, Estienne C. Swart
{"title":"ISWI1复合蛋白促进了鹦鹉螺的发育基因组编辑","authors":"Aditi Singh, Lilia Häußermann, Christiane Emmerich, Emily Nischwitz, Brandon KB Seah, Falk Butter, Mariusz Nowacki, Estienne C. Swart","doi":"10.1101/gr.278402.123","DOIUrl":null,"url":null,"abstract":"One of the most extensive forms of natural genome editing occurs in ciliates, a group of microbial eukaryotes. Ciliate germline and somatic genomes are contained in distinct nuclei within the same cell. During the massive reorganization process of somatic genome development, ciliates eliminate tens of thousands of DNA sequences from a germline genome copy. Recently, we showed that the chromatin remodeler ISWI1 is required for somatic genome development in the ciliate <em>Paramecium tetraurelia</em>. Here, we describe two high similarity paralogous proteins, ICOPa and ICOPb, essential for their genome editing. ICOPa and ICOPb are highly divergent from known proteins; the only domain detected showed distant homology to the WSD (WHIM2+WHIM3) motif. We show that both ICOPa and ICOPb interact with the chromatin remodeler ISWI1. Upon ICOP knockdown, changes in alternative DNA excision boundaries and nucleosome densities are similar to those observed for <em>ISWI1</em> knockdown. We thus propose that a complex comprising ISWI1 and either or both ICOPa and ICOPb are needed for <em>Paramecium's</em> precise genome editing.","PeriodicalId":12678,"journal":{"name":"Genome research","volume":"9 1","pages":""},"PeriodicalIF":6.2000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"ISWI1 complex proteins facilitate developmental genome editing in Paramecium\",\"authors\":\"Aditi Singh, Lilia Häußermann, Christiane Emmerich, Emily Nischwitz, Brandon KB Seah, Falk Butter, Mariusz Nowacki, Estienne C. Swart\",\"doi\":\"10.1101/gr.278402.123\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"One of the most extensive forms of natural genome editing occurs in ciliates, a group of microbial eukaryotes. Ciliate germline and somatic genomes are contained in distinct nuclei within the same cell. During the massive reorganization process of somatic genome development, ciliates eliminate tens of thousands of DNA sequences from a germline genome copy. Recently, we showed that the chromatin remodeler ISWI1 is required for somatic genome development in the ciliate <em>Paramecium tetraurelia</em>. Here, we describe two high similarity paralogous proteins, ICOPa and ICOPb, essential for their genome editing. ICOPa and ICOPb are highly divergent from known proteins; the only domain detected showed distant homology to the WSD (WHIM2+WHIM3) motif. We show that both ICOPa and ICOPb interact with the chromatin remodeler ISWI1. Upon ICOP knockdown, changes in alternative DNA excision boundaries and nucleosome densities are similar to those observed for <em>ISWI1</em> knockdown. We thus propose that a complex comprising ISWI1 and either or both ICOPa and ICOPb are needed for <em>Paramecium's</em> precise genome editing.\",\"PeriodicalId\":12678,\"journal\":{\"name\":\"Genome research\",\"volume\":\"9 1\",\"pages\":\"\"},\"PeriodicalIF\":6.2000,\"publicationDate\":\"2024-11-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Genome research\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1101/gr.278402.123\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genome research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1101/gr.278402.123","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

纤毛虫是一类微生物真核生物,是自然基因组编辑最广泛的形式之一。纤毛虫的生殖基因组和体细胞基因组包含在同一细胞内不同的细胞核中。在体细胞基因组发育的大规模重组过程中,纤毛虫会从生殖基因组拷贝中删除数以万计的 DNA 序列。最近,我们发现染色质重塑器 ISWI1 是纤毛虫四膜虫体细胞基因组发育所必需的。在这里,我们描述了两个高度相似的同源蛋白 ICOPa 和 ICOPb,它们对基因组编辑至关重要。ICOPa 和 ICOPb 与已知的蛋白质有很大差异;检测到的唯一结构域与 WSD(WHIM2+WHIM3)基团有很远的同源性。我们的研究表明,ICOPa 和 ICOPb 都与染色质重塑因子 ISWI1 相互作用。敲除 ICOP 后,替代 DNA 切割边界和核小体密度的变化与敲除 ISWI1 后观察到的变化相似。因此,我们认为副鳞虫的精确基因组编辑需要一个由 ISWI1 和 ICOPa 或 ICOPb 组成的复合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
ISWI1 complex proteins facilitate developmental genome editing in Paramecium
One of the most extensive forms of natural genome editing occurs in ciliates, a group of microbial eukaryotes. Ciliate germline and somatic genomes are contained in distinct nuclei within the same cell. During the massive reorganization process of somatic genome development, ciliates eliminate tens of thousands of DNA sequences from a germline genome copy. Recently, we showed that the chromatin remodeler ISWI1 is required for somatic genome development in the ciliate Paramecium tetraurelia. Here, we describe two high similarity paralogous proteins, ICOPa and ICOPb, essential for their genome editing. ICOPa and ICOPb are highly divergent from known proteins; the only domain detected showed distant homology to the WSD (WHIM2+WHIM3) motif. We show that both ICOPa and ICOPb interact with the chromatin remodeler ISWI1. Upon ICOP knockdown, changes in alternative DNA excision boundaries and nucleosome densities are similar to those observed for ISWI1 knockdown. We thus propose that a complex comprising ISWI1 and either or both ICOPa and ICOPb are needed for Paramecium's precise genome editing.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Genome research
Genome research 生物-生化与分子生物学
CiteScore
12.40
自引率
1.40%
发文量
140
审稿时长
6 months
期刊介绍: Launched in 1995, Genome Research is an international, continuously published, peer-reviewed journal that focuses on research that provides novel insights into the genome biology of all organisms, including advances in genomic medicine. Among the topics considered by the journal are genome structure and function, comparative genomics, molecular evolution, genome-scale quantitative and population genetics, proteomics, epigenomics, and systems biology. The journal also features exciting gene discoveries and reports of cutting-edge computational biology and high-throughput methodologies. New data in these areas are published as research papers, or methods and resource reports that provide novel information on technologies or tools that will be of interest to a broad readership. Complete data sets are presented electronically on the journal''s web site where appropriate. The journal also provides Reviews, Perspectives, and Insight/Outlook articles, which present commentary on the latest advances published both here and elsewhere, placing such progress in its broader biological context.
期刊最新文献
Modeling gene interactions in polygenic prediction via geometric deep learning High-quality sika deer omics data and integrative analysis reveal genic and cellular regulation of antler regeneration ISWI1 complex proteins facilitate developmental genome editing in Paramecium Haplotype-resolved genome and population genomics of the threatened garden dormouse in Europe. Multisample motif discovery and visualization for tandem repeats
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1