<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Muller GA</submitter><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Institute of General Medical Sciences</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>2909-2919</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9201786</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>41(21)</volume><pubmed_abstract>Proper progression through the cell-division cycle is critical to normal development and homeostasis and is necessarily misregulated in cancer. The key to cell-cycle regulation is the control of two waves of transcription that occur at the onset of DNA replication (S phase) and mitosis (M phase). MuvB complexes play a central role in the regulation of these genes. When cells are not actively dividing, the MuvB complex DREAM represses G1/S and G2/M genes. Remarkably, MuvB also forms activator complexes together with the oncogenic transcription factors B-MYB and FOXM1 that are required for the expression of the mitotic genes in G2/M. Despite this essential role in the control of cell division and the relationship to cancer, it has been unclear how MuvB complexes inhibit and stimulate gene ex</pubmed_abstract><journal>Oncogene</journal><pubmed_title>Structure and function of MuvB complexes.</pubmed_title><pmcid>PMC9201786</pmcid><funding_grant_id>R01 GM124148</funding_grant_id><funding_grant_id>R01 GM127707</funding_grant_id><funding_grant_id>R01GM127707</funding_grant_id><funding_grant_id>T32 CA009302</funding_grant_id><funding_grant_id>R01 CA228413</funding_grant_id><pubmed_authors>Asthana A</pubmed_authors><pubmed_authors>Rubin SM</pubmed_authors><pubmed_authors>Muller GA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Structure and function of MuvB complexes.</name><description>Proper progression through the cell-division cycle is critical to normal development and homeostasis and is necessarily misregulated in cancer. The key to cell-cycle regulation is the control of two waves of transcription that occur at the onset of DNA replication (S phase) and mitosis (M phase). MuvB complexes play a central role in the regulation of these genes. When cells are not actively dividing, the MuvB complex DREAM represses G1/S and G2/M genes. Remarkably, MuvB also forms activator complexes together with the oncogenic transcription factors B-MYB and FOXM1 that are required for the expression of the mitotic genes in G2/M. Despite this essential role in the control of cell division and the relationship to cancer, it has been unclear how MuvB complexes inhibit and stimulate gene ex</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-04-04T22:33:37.14Z</modification><creation>2025-02-19T03:23:50.391Z</creation></dates><accession>S-EPMC9201786</accession><cross_references><pubmed>35468940</pubmed><doi>10.1038/s41388-022-02321-x</doi></cross_references></HashMap>