Transcriptional regulation by the KMT2 histone H3K4 methyltransferases

Cited 10 time in webofscience Cited 7 time in scopus
  • Hit : 487
  • Download : 0
DC FieldValueLanguage
dc.contributor.authorPark, Kihyunko
dc.contributor.authorKim, Jung-Aeko
dc.contributor.authorKim, Jaehoonko
dc.date.accessioned2020-06-22T05:20:12Z-
dc.date.available2020-06-22T05:20:12Z-
dc.date.created2020-06-15-
dc.date.issued2020-07-
dc.identifier.citationBIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, v.1863, no.7, pp.194545-
dc.identifier.issn1874-9399-
dc.identifier.urihttp://hdl.handle.net/10203/274758-
dc.description.abstractHistone lysine methyltransferase 2 (KMT2) proteins form multimeric enzymatic complexes that methylate lysine 4 on histone H3 (H3K4) at transcription regulatory elements in the genome. A strong association of H3K4 methylation with active transcription has led to intense efforts to reveal the functional involvement of KMT2 complexes in transcriptional regulation. A number of biochemical and cellular studies have shown that KMT2 complexes regulate transcription of target genes via H3K4 methylation. However, in many cases, loss of KMT2 complex enzymatic activity fails to fully account for observed transcriptional defects. Accumulating evidence indicates that, in certain contexts, KMT2 complex-mediated transcriptional regulation can occur in an H3K4 methylation-independent manner. Here, we comprehensively review functions of KMT2 complexes in gene expression, focusing on what we currently know about the molecular mechanisms by which the KMT2 complexes regulate transcription. We also discuss how aberrant transcriptional regulation by KMT2 complexes contributes to different human diseases, such as cancer.-
dc.languageEnglish-
dc.publisherELSEVIER-
dc.titleTranscriptional regulation by the KMT2 histone H3K4 methyltransferases-
dc.typeArticle-
dc.identifier.wosid000536293700004-
dc.identifier.scopusid2-s2.0-85083704146-
dc.type.rimsART-
dc.citation.volume1863-
dc.citation.issue7-
dc.citation.beginningpage194545-
dc.citation.publicationnameBIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS-
dc.identifier.doi10.1016/j.bbagrm.2020.194545-
dc.contributor.localauthorKim, Jaehoon-
dc.contributor.nonIdAuthorKim, Jung-Ae-
dc.description.isOpenAccessN-
dc.type.journalArticleReview-
dc.subject.keywordAuthorHistone H3K4 methylation-
dc.subject.keywordAuthorKMT2 family methyltransferases-
dc.subject.keywordAuthorKMT2 complexes-
dc.subject.keywordAuthorGene expression-
dc.subject.keywordAuthorTranscriptional regulation-
dc.subject.keywordPlusCELL-CYCLE PROGRESSION-
dc.subject.keywordPlusEMBRYONIC STEM-CELLS-
dc.subject.keywordPlusSET DOMAIN-
dc.subject.keywordPlusTUMOR-SUPPRESSOR-
dc.subject.keywordPlusCOMPASS FAMILY-
dc.subject.keywordPlusLYSINE 4-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusTARGET GENES-
dc.subject.keywordPlusPHD FINGER-
Appears in Collection
BS-Journal Papers(저널논문)
Files in This Item
There are no files associated with this item.
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 10 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0