SWI/SNF regulates half of its targets without the need of ATP-driven nucleosome remodeling by BrahmaShow others and affiliations
Number of Authors: 62018 (English)In: BMC Genomics, E-ISSN 1471-2164, Vol. 19, article id 367
Article in journal (Refereed) Published
Abstract [en]
Background: Brahma (BRM) is the only catalytic subunit of the SVVI/SNF chromatin-remodeling complex of Drosophila melanogaster. The function of SWI/SNF in transcription has long been attributed to its ability to remodel nucleosomes, which requires the ATPase activity of BRM. However, recent studies have provided evidence for a non-catalytic function of BRM in the transcriptional regulation of a few specific genes.
Results: Here we have used RNA-seq and ChIP-seq to identify the BRM target genes in 52 cells, and we have used a catalytically inactive BRM mutant (K804R) that is unable to hydrolyze ATP to investigate the magnitude of the non-catalytic function of BRM in transcription regulation. We show that 49% of the BRM target genes in 52 cells are regulated through mechanisms that do not require BRM to have an ATPase activity. We also show that the catalytic and non-catalytic mechanisms of SVVI/SNF regulation operate on two subsets of genes that differ in promoter architecture and are linked to different biological processes.
Conclusions: This study shows that the non-catalytic role of SWI/SNF in transcription regulation is far more prevalent than previously anticipated and that the genes that are regulated by SVVI/SNF through ATPase-dependent and ATPase-independent mechanisms have specialized roles in different cellular and developmental processes.
Place, publisher, year, edition, pages
2018. Vol. 19, article id 367
Keywords [en]
SWI/SNF, Gene expression, Transcription regulation, Drosophila melanogaster
National Category
Environmental Biotechnology Biological Sciences
Identifiers
URN: urn:nbn:se:su:diva-157741DOI: 10.1186/s12864-018-4746-2ISI: 000432702400002PubMedID: 29776334OAI: oai:DiVA.org:su-157741DiVA, id: diva2:1236658
2018-08-032018-08-032024-01-17Bibliographically approved