Subunits of the PBAP Chromatin Remodeler Are Capable of Mediating Enhancer-Driven Transcription in .

TitleSubunits of the PBAP Chromatin Remodeler Are Capable of Mediating Enhancer-Driven Transcription in .
Publication TypeJournal Article
Year of Publication2021
AuthorsShidlovskii, YV, Bylino, OV, Shaposhnikov, AV, Kachaev, ZM, Lebedeva, LA, Kolesnik, VV, Amendola, D, De Simone, G, Formicola, N, Schedl, P, Digilio, FAnna, Giordano, E
JournalInt J Mol Sci
Volume22
Issue6
Date Published2021 Mar 11
ISSN1422-0067
KeywordsAnimals, Animals, Genetically Modified, Chromatin Assembly and Disassembly, Drosophila melanogaster, Drosophila Proteins, Enhancer Elements, Genetic, Fluorescent Antibody Technique, Indirect, Humans, In Situ Hybridization, Models, Genetic, Promoter Regions, Genetic, Protein Subunits, Transcription Factors, Transcription, Genetic, Transcriptional Activation
Abstract

<p>The chromatin remodeler SWI/SNF is an important participant in gene activation, functioning predominantly by opening the chromatin structure on promoters and enhancers. Here, we describe its novel mode of action in which SWI/SNF factors mediate the targeted action of an enhancer. We studied the functions of two signature subunits of PBAP subfamily, BAP170 and SAYP, in . These subunits were stably tethered to a transgene reporter carrying the core promoter. The tethered subunits mediate transcription of the reporter in a pattern that is generated by enhancers close to the insertion site in multiple loci throughout the genome. Both tethered SAYP and BAP170 recruit the whole PBAP complex to the reporter promoter. However, we found that BAP170-dependent transcription is more resistant to the depletion of other PBAP subunits, suggesting that BAP170 may play a more critical role in establishing enhancer-dependent transcription.</p>

DOI10.3390/ijms22062856
Alternate JournalInt J Mol Sci
PubMed ID33799739
PubMed Central IDPMC7999800
Grant List19-34-51003 / / Russian Foundation for Basic Research /
"BioIndustrial Processess" (BIP) / / Italian POR /