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TSC22D、WNK 和 NRBP 基因家族表现出功能缓冲作用,并与后生动物一起进化以调节细胞体积。

The TSC22D, WNK, and NRBP gene families exhibit functional buffering and evolved with Metazoa for cell volume regulation.

机构信息

Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada.

Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.

出版信息

Cell Rep. 2024 Jul 23;43(7):114417. doi: 10.1016/j.celrep.2024.114417. Epub 2024 Jul 8.

Abstract

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.

摘要

感知和响应渗透波动的能力对于维持细胞完整性至关重要。我们使用基因共必需性分析来鉴定 TSC22D2、WNK1 和 NRBP1 之间在调节细胞体积稳态方面的未被认识到的关系。所有这些基因都有同源基因,并且在渗透压感应和细胞体积控制方面具有功能缓冲作用。在高渗应激后的几秒钟内,TSC22D、WNK 和 NRBP 家族成员物理上结合成生物分子凝聚物,这一过程依赖于内在无序区域 (IDR)。对这些蛋白家族在后生动物中的广泛研究表明,TSC22D 基因与 NRBPs 中的一个特定结合 TSC22D 蛋白的结构域一起进化,我们将其称为 NbrT(与 TSC22D 结合的 NRBP 结构域),这种共同进化伴随着 WNK 家族激酶中快速 IDR 长度的扩张。我们的研究揭示了 TSC22D、WNK 和 NRBP 基因在后生动物中进化,以共同调节细胞对渗透压变化的快速体积变化。

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