{"title":"右开放阅读框激酶1 (RIOK1)的磷酸化调控网络,其功能相关性和癌症治疗前景。","authors":"Amal Fahma, Leona Dcunha, Suhail Subair, Athira Perunelly Gopalakrishnan, Levin John, Samseera Ummar, Prathik Basthikoppa Shivamurthy, Poornima Ramesh, Rajesh Raju, Yashwanth Subbannayya","doi":"10.1177/15578100251378038","DOIUrl":null,"url":null,"abstract":"<p><p>Right open reading frame kinase 1 (RIOK1) is an atypical kinase involved in ribosome biogenesis, cell cycle progression, and chromosome organization. Its overexpression is linked to tumor progression, metastasis, and chemoresistance, while its absence alters protein phosphorylation across various biological processes. Although the oncogenic role of RIOK1 is recognized, its phospho-regulatory network and the functional relevance of its phosphorylation sites remain unknown. Here, we present the first large-scale phosphoproteomic analysis of RIOK1. Through a systematic assembly of 671 mass spectrometry-based datasets and 157 datasets that quantified RIOK1 phosphopeptides in different experimental conditions, we compiled 13 RIOK1 phosphorylation sites. Notably, phosphorylation at S21 and S22 was predominant, observed in 83% of phosphoproteomics datasets, highlighting their functional significance, and these sites may have a role in RIOK1's interaction with the protein arginine methyltransferase 5 complex. We identified co-differentially regulated phosphorylation events in potential upstream kinases and experimentally validated interactors, providing insights into RIOK1's broader signaling context. The phosphorylation sites in five potential upstream kinases (eukaryotic translation initiation factor 2 alpha kinase 4, ataxia telangiectasia mutated protein kinase, B-Raf proto-oncogene, mitogen-activated protein kinase kinase kinase 3, and polo-like kinase 1) co-differentially regulated with RIOK1 were identified, which regulate their activity in concert with RIOK1 in cancers. Together, this study represents the first comprehensive map to date of RIOK1 phosphorylation and its regulatory associations, highlighting its potential as a therapeutic target in cancers.</p>","PeriodicalId":19530,"journal":{"name":"Omics A Journal of Integrative Biology","volume":" ","pages":"515-527"},"PeriodicalIF":1.6000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phospho-Regulatory Network of the Right Open Reading Frame Kinase 1 (RIOK1), Its Functional Relevance, and Cancer Treatment Prospects.\",\"authors\":\"Amal Fahma, Leona Dcunha, Suhail Subair, Athira Perunelly Gopalakrishnan, Levin John, Samseera Ummar, Prathik Basthikoppa Shivamurthy, Poornima Ramesh, Rajesh Raju, Yashwanth Subbannayya\",\"doi\":\"10.1177/15578100251378038\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Right open reading frame kinase 1 (RIOK1) is an atypical kinase involved in ribosome biogenesis, cell cycle progression, and chromosome organization. Its overexpression is linked to tumor progression, metastasis, and chemoresistance, while its absence alters protein phosphorylation across various biological processes. Although the oncogenic role of RIOK1 is recognized, its phospho-regulatory network and the functional relevance of its phosphorylation sites remain unknown. Here, we present the first large-scale phosphoproteomic analysis of RIOK1. Through a systematic assembly of 671 mass spectrometry-based datasets and 157 datasets that quantified RIOK1 phosphopeptides in different experimental conditions, we compiled 13 RIOK1 phosphorylation sites. Notably, phosphorylation at S21 and S22 was predominant, observed in 83% of phosphoproteomics datasets, highlighting their functional significance, and these sites may have a role in RIOK1's interaction with the protein arginine methyltransferase 5 complex. We identified co-differentially regulated phosphorylation events in potential upstream kinases and experimentally validated interactors, providing insights into RIOK1's broader signaling context. The phosphorylation sites in five potential upstream kinases (eukaryotic translation initiation factor 2 alpha kinase 4, ataxia telangiectasia mutated protein kinase, B-Raf proto-oncogene, mitogen-activated protein kinase kinase kinase 3, and polo-like kinase 1) co-differentially regulated with RIOK1 were identified, which regulate their activity in concert with RIOK1 in cancers. Together, this study represents the first comprehensive map to date of RIOK1 phosphorylation and its regulatory associations, highlighting its potential as a therapeutic target in cancers.</p>\",\"PeriodicalId\":19530,\"journal\":{\"name\":\"Omics A Journal of Integrative Biology\",\"volume\":\" \",\"pages\":\"515-527\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Omics A Journal of Integrative Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1177/15578100251378038\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/9/22 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Omics A Journal of Integrative Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1177/15578100251378038","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/9/22 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Phospho-Regulatory Network of the Right Open Reading Frame Kinase 1 (RIOK1), Its Functional Relevance, and Cancer Treatment Prospects.
Right open reading frame kinase 1 (RIOK1) is an atypical kinase involved in ribosome biogenesis, cell cycle progression, and chromosome organization. Its overexpression is linked to tumor progression, metastasis, and chemoresistance, while its absence alters protein phosphorylation across various biological processes. Although the oncogenic role of RIOK1 is recognized, its phospho-regulatory network and the functional relevance of its phosphorylation sites remain unknown. Here, we present the first large-scale phosphoproteomic analysis of RIOK1. Through a systematic assembly of 671 mass spectrometry-based datasets and 157 datasets that quantified RIOK1 phosphopeptides in different experimental conditions, we compiled 13 RIOK1 phosphorylation sites. Notably, phosphorylation at S21 and S22 was predominant, observed in 83% of phosphoproteomics datasets, highlighting their functional significance, and these sites may have a role in RIOK1's interaction with the protein arginine methyltransferase 5 complex. We identified co-differentially regulated phosphorylation events in potential upstream kinases and experimentally validated interactors, providing insights into RIOK1's broader signaling context. The phosphorylation sites in five potential upstream kinases (eukaryotic translation initiation factor 2 alpha kinase 4, ataxia telangiectasia mutated protein kinase, B-Raf proto-oncogene, mitogen-activated protein kinase kinase kinase 3, and polo-like kinase 1) co-differentially regulated with RIOK1 were identified, which regulate their activity in concert with RIOK1 in cancers. Together, this study represents the first comprehensive map to date of RIOK1 phosphorylation and its regulatory associations, highlighting its potential as a therapeutic target in cancers.
期刊介绍:
OMICS: A Journal of Integrative Biology is the only peer-reviewed journal covering all trans-disciplinary OMICs-related areas, including data standards and sharing; applications for personalized medicine and public health practice; and social, legal, and ethics analysis. The Journal integrates global high-throughput and systems approaches to 21st century science from “cell to society” – seen from a post-genomics perspective.