<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Xiaochun Yu</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0018254000</full_dataset_link><submitter_email>yuxiaochun@westlake.edu.cn</submitter_email><submitter_affiliation>Westlake University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>VRK1 phosphorylates SRRM2 for the regulation of splicing of DNA damage repair factors</name><description>Vaccinia-related kinase 1 (VRK1) is a nuclear serine/threonine kinase that contributes to genome stability through the phosphorylation of diverse substrates. This study investigated whether VRK1 regulates pre-messenger RNA splicing through serine/arginine repetitive matrix protein 2 (SRRM2), a nuclear speckle-associated splicing scaffold. Messenger RNA sequencing was performed in control HEK293T cells, VRK1-knockout HEK293T cells, and SRRM2-depleted HEK293T cells. Alternative splicing events were analyzed using replicate Multivariate Analysis of Transcript Splicing. Most differential alternative splicing events detected following VRK1 knockout or SRRM2 depletion were skipped-exon events. A subset of skipped-exon events was shared between VRK1-knockout and SRRM2-depleted cells, and the corresponding genes were enriched in DNA repair-related pathways. These data support a role for the VRK1-SRRM2 regulatory axis in maintaining the efficient alternative splicing of DNA damage response-related transcripts.</description><dates><publication>Thu Jul 09 00:00:00 GMT+01:00 2026</publication></dates><accession>PXD080922</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>