基因家族
生物
基因
渗透浓度
渗透性休克
细胞生物学
激酶
蛋白质家族
基因复制
蛋白质结构域
遗传学
基因表达
生物化学
作者
Yu-Xi Xiao,Seon Yong Lee,Magali Aguilera-Uribe,Reuben Samson,Aaron Au,Yukti Khanna,Zetao Liu,Ran Cheng,Kamaldeep Aulakh,Jiarun Wei,Adrian Granda Farias,Taylor Reilly,Saba Birkadze,Andrea Habsid,Kevin R. Brown,Katherine Chan,Patricia Mero,Jie Huang,Maximilian Billmann,Mahfuzur Rahman
出处
期刊:Cell Reports
[Cell Press]
日期:2024-07-01
卷期号:43 (7): 114417-114417
被引量:7
标识
DOI:10.1016/j.celrep.2024.114417
摘要
The ability to sense and respond to osmotic fluctuations is critical for the maintenance of cellular integrity. We used gene co-essentiality analysis to identify an unappreciated relationship between TSC22D2, WNK1, and NRBP1 in regulating cell volume homeostasis. All of these genes have paralogs and are functionally buffered for osmo-sensing and cell volume control. Within seconds of hyperosmotic stress, TSC22D, WNK, and NRBP family members physically associate into biomolecular condensates, a process that is dependent on intrinsically disordered regions (IDRs). A close examination of these protein families across metazoans revealed that TSC22D genes evolved alongside a domain in NRBPs that specifically binds to TSC22D proteins, which we have termed NbrT (NRBP binding region with TSC22D), and this co-evolution is accompanied by rapid IDR length expansion in WNK-family kinases. Our study reveals that TSC22D, WNK, and NRBP genes evolved in metazoans to co-regulate rapid cell volume changes in response to osmolarity.
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