外泌体复合物组分1和2对哺乳动物的早期发育至关重要。

IF 1 4区 生物学 Q4 DEVELOPMENTAL BIOLOGY Gene Expression Patterns Pub Date : 2023-11-07 DOI:10.1016/j.gep.2023.119346
Sanjana Srinivasan, Xinjian He, Sarah Mirza, Jesse Mager
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引用次数: 0

摘要

外泌体复合物组分1和2(EXOSC1和2)是RNA外泌体复合体中的两种蛋白质,其主要功能是5’→ 3'核糖核酸的降解和加工。RNA外泌体复合体由九个亚基组成,形成两个独立的成分:S1/KH帽和PH核心。EXOSC1和2都是S1/KH帽的一部分,并参与结合新生RNA。作为敲除小鼠项目产生的早期致死等位基因的系统表征的一部分,我们检测了Exosc1和Exosc2纯合无效(突变)胚胎,以确定缺乏其功能的胚胎的发育和分子表型。我们的研究表明,Exosc1缺失的胚胎植入并形成卵子圆柱体,但发育迟缓,无法在胚胎第7.5天开始原肠胚形成。相反,Exosc2缺失胚胎在植入期是致命的,虽然它们在E3.5时确实形成了形态正常的胚泡,但在植入后阶段无法恢复。我们发现在Exosc1和Exosc2突变胚胎中都缺乏阶段特异性发育和谱系规范的改变,并得出结论,这些基因对哺乳动物早期发育的成功进展至关重要。
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Exosome complex components 1 and 2 are vital for early mammalian development

Exosome Complex Components 1 and 2 (EXOSC1 and 2) are two proteins in the RNA Exosome complex whose main function is 5’ → 3’ RNA degradation and processing. The RNA exosome complex is comprised of nine subunits that form two separate components: the S1/KH cap and the PH-core. EXOSC1 and 2 are both part of the S1/KH cap and are involved in binding nascent RNA. As part of a systemic characterization of early lethal alleles produced by the Knockout Mouse Project, we have examined Exosc1 and Exosc2 homozygous null (mutant) embryos to determine developmental and molecular phenotypes of embryos lacking their functions. Our studies reveal that Exosc1 null embryos implant and form an egg cylinder but are developmentally delayed and fail to initiate gastrulation by embryonic day 7.5. In contrast, Exosc2 null embryos are lethal during peri-implantation stages, and while they do form a morphologically normal blastocyst at E3.5, they cannot be recovered at post-implantation stages. We show the absence of stage-specific developmental and altered lineage-specification in both Exosc1 and Exosc2 mutant embryos and conclude that these genes are essential for the successful progression through early mammalian development.

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来源期刊
Gene Expression Patterns
Gene Expression Patterns 生物-发育生物学
CiteScore
2.30
自引率
0.00%
发文量
42
审稿时长
35 days
期刊介绍: Gene Expression Patterns is devoted to the rapid publication of high quality studies of gene expression in development. Studies using cell culture are also suitable if clearly relevant to development, e.g., analysis of key regulatory genes or of gene sets in the maintenance or differentiation of stem cells. Key areas of interest include: -In-situ studies such as expression patterns of important or interesting genes at all levels, including transcription and protein expression -Temporal studies of large gene sets during development -Transgenic studies to study cell lineage in tissue formation
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