Set2 methyltransferase facilitates cell cycle progression by maintaining transcriptional fidelity

التفاصيل البيبلوغرافية
العنوان: Set2 methyltransferase facilitates cell cycle progression by maintaining transcriptional fidelity
المؤلفون: Raghuvar Dronamraju, Brian D. Strahl, Umut Eser, Deepak Kumar Jha, Rajarshi Choudhury, Michael J. Emanuele, Daniel Dominguez, W. Kimryn Rathmell, Alexander T. Adams, Yun Chen Chiang, L. Stirling Churchman
المصدر: Nucleic Acids Research
سنة النشر: 2017
مصطلحات موضوعية: 0301 basic medicine, Methyltransferase, Saccharomyces cerevisiae Proteins, Transcription, Genetic, Cdc20 Proteins, Saccharomyces cerevisiae, Biology, Methylation, Anaphase-Promoting Complex-Cyclosome, Histones, 03 medical and health sciences, Histone H3, Gene Expression Regulation, Fungal, Genetics, Humans, Gene, Molecular Biology, Regulator gene, Regulation of gene expression, Lysine, Nocodazole, Cell Cycle, Histone-Lysine N-Methyltransferase, Methyltransferases, Cell cycle, Biological Evolution, Tubulin Modulators, Chromatin, Cell biology, 030104 developmental biology, Proteolysis, Protein Processing, Post-Translational
الوصف: Methylation of histone H3 lysine 36 (H3K36me) by yeast Set2 is critical for the maintenance of chromatin structure and transcriptional fidelity. However, we do not know the full range of Set2/H3K36me functions or the scope of mechanisms that regulate Set2-dependent H3K36 methylation. Here, we show that the APC/CCDC20 complex regulates Set2 protein abundance during the cell cycle. Significantly, absence of Set2-mediated H3K36me causes a loss of cell cycle control and pronounced defects in the transcriptional fidelity of cell cycle regulatory genes, a class of genes that are generally long, hence highly dependent on Set2/H3K36me for their transcriptional fidelity. Because APC/C also controls human SETD2, and SETD2 likewise regulates cell cycle progression, our data imply an evolutionarily conserved cell cycle function for Set2/SETD2 that may explain why recurrent mutations of SETD2 contribute to human disease.
تدمد: 1362-4962
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d3aefaee495a6830142c610fa3ce625Test
https://pubmed.ncbi.nlm.nih.gov/29294086Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....8d3aefaee495a6830142c610fa3ce625
قاعدة البيانات: OpenAIRE