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Rpd3L HDAC links H3K4me3 to transcriptional repression memory

Transcriptional memory is critical for the faster reactivation of necessary genes upon environmental changes and requires that the genes were previously in an active state. However, whether transcriptional repression also displays ‘memory’ of the prior transcriptionally inactive state remains unknow...

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Detalles Bibliográficos
Autores principales: Lee, Bo Bae, Choi, Ahyoung, Kim, Ji Hyun, Jun, Yukyung, Woo, Hyeonju, Ha, So Dam, Yoon, Chae Young, Hwang, Jin-Taek, Steinmetz, Lars, Buratowski, Stephen, Lee, Sanghyuk, Kim, Hye Young, Kim, TaeSoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144869/
https://www.ncbi.nlm.nih.gov/pubmed/29982589
http://dx.doi.org/10.1093/nar/gky573
Descripción
Sumario:Transcriptional memory is critical for the faster reactivation of necessary genes upon environmental changes and requires that the genes were previously in an active state. However, whether transcriptional repression also displays ‘memory’ of the prior transcriptionally inactive state remains unknown. In this study, we show that transcriptional repression of ∼540 genes in yeast occurs much more rapidly if the genes have been previously repressed during carbon source shifts. This novel transcriptional response has been termed transcriptional repression memory (TREM). Interestingly, Rpd3L histone deacetylase (HDAC), targeted to active promoters induces TREM. Mutants for Rpd3L exhibit increased acetylation at active promoters and delay TREM significantly. Surprisingly, the interaction between H3K4me3 and Rpd3L via the Pho23 PHD finger is critical to promote histone deacetylation and TREM by Rpd3L. Therefore, we propose that an active mark, H3K4me3 enriched at active promoters, instructs Rpd3L HDAC to induce histone deacetylation and TREM.