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