Department of Molecular Biology, College of Agriculture, Life Sciences and Natural Resources, University of Wyoming, Laramie, Wyoming, United States of America.
PLoS Genet. 2024 Aug 22;20(8):e1011219. doi: 10.1371/journal.pgen.1011219. eCollection 2024 Aug.
Protein tyrosine phosphatases non-receptor type (PTPNs) have been studied extensively in the context of the adaptive immune system; however, their roles beyond immunoregulation are less well explored. Here we identify novel functions for the conserved C. elegans phosphatase PTPN-22, establishing its role in nematode molting, cell adhesion, and cytoskeletal regulation. Through a non-biased genetic screen, we found that loss of PTPN-22 phosphatase activity suppressed molting defects caused by loss-of-function mutations in the conserved NIMA-related kinases NEKL-2 (human NEK8/NEK9) and NEKL-3 (human NEK6/NEK7), which act at the interface of membrane trafficking and actin regulation. To better understand the functions of PTPN-22, we carried out proximity labeling studies to identify candidate interactors of PTPN-22 during development. Through this approach we identified the CDC42 guanine-nucleotide exchange factor DNBP-1 (human DNMBP) as an in vivo partner of PTPN-22. Consistent with this interaction, loss of DNBP-1 also suppressed nekl-associated molting defects. Genetic analysis, co-localization studies, and proximity labeling revealed roles for PTPN-22 in several epidermal adhesion complexes, including C. elegans hemidesmosomes, suggesting that PTPN-22 plays a broad role in maintaining the structural integrity of tissues. Localization and proximity labeling also implicated PTPN-22 in functions connected to nucleocytoplasmic transport and mRNA regulation, particularly within the germline, as nearly one-third of proteins identified by PTPN-22 proximity labeling are known P granule components. Collectively, these studies highlight the utility of combined genetic and proteomic approaches for identifying novel gene functions.
蛋白酪氨酸磷酸酶非受体型(PTPNs)在适应性免疫系统的背景下得到了广泛研究;然而,它们在免疫调节之外的作用还不太清楚。在这里,我们确定了保守的秀丽隐杆线虫磷酸酶 PTPN-22 的新功能,证明了它在线虫蜕皮、细胞黏附和细胞骨架调节中的作用。通过非偏见的遗传筛选,我们发现 PTPN-22 磷酸酶活性的丧失抑制了保守的 NIMA 相关激酶 NEKL-2(人类 NEK8/NEK9)和 NEKL-3(人类 NEK6/NEK7)功能丧失突变引起的蜕皮缺陷,这些激酶在膜运输和肌动蛋白调节的界面处起作用。为了更好地理解 PTPN-22 的功能,我们进行了接近标记研究,以确定 PTPN-22 在发育过程中的候选相互作用蛋白。通过这种方法,我们鉴定了 CDC42 鸟嘌呤核苷酸交换因子 DNBP-1(人类 DNMBP)作为 PTPN-22 的体内伴侣。与这种相互作用一致,DNBP-1 的缺失也抑制了与 nekl 相关的蜕皮缺陷。遗传分析、共定位研究和接近标记揭示了 PTPN-22 在几个表皮黏附复合物中的作用,包括秀丽隐杆线虫半桥粒,表明 PTPN-22 在维持组织结构完整性方面发挥着广泛的作用。定位和接近标记也暗示了 PTPN-22 在与核质转运和 mRNA 调节相关的功能中的作用,特别是在生殖系中,因为通过 PTPN-22 接近标记鉴定的近三分之一的蛋白质是已知的 P 颗粒成分。总之,这些研究强调了结合遗传和蛋白质组学方法识别新基因功能的效用。