SAF-A forms a complex with BRG1 and both components are required for RNA polymerase II mediated transcription

Autor: Rikard Runnberg, Tomas Simonsson, Jessica Ryme, Stina Simonsson, Dzeneta Vizlin-Hodzic
Jazyk: angličtina
Rok vydání: 2011
Předmět:
Transcription
Genetic

DNA transcription
lcsh:Medicine
RNA polymerase II
Heterogeneous-Nuclear Ribonucleoprotein U
Models
Biological

Biochemistry
Cell Line
Molecular Genetics
Mice
Molecular cell biology
RNA interference
Nucleic Acids
RNA polymerase I
Genetics
Animals
Humans
Gene Regulation
RNA
Messenger

lcsh:Science
RNA polymerase II holoenzyme
Biology
Embryonic Stem Cells
Multidisciplinary
Microscopy
Confocal

biology
General transcription factor
Chromosome Biology
fungi
lcsh:R
DNA Helicases
Nuclear Proteins
Cell Differentiation
DNA-Directed RNA Polymerases
Molecular biology
DNA-Binding Proteins
biology.protein
Transcription factor II F
lcsh:Q
Transcription factor II E
RNA Polymerase II
Gene expression
Transcription factor II D
Transcription factor II B
Protein Binding
Transcription Factors
Research Article
Developmental Biology
Zdroj: PLoS ONE, Vol 6, Iss 12, p e28049 (2011)
PLoS ONE
ISSN: 1932-6203
Popis: BACKGROUND: Scaffold attachment factor A (SAF-A) participates in the regulation of gene expression by organizing chromatin into transcriptionally active domains and by interacting directly with RNA polymerase II. METHODOLOGY: Here we use co-localization, co-immunoprecipitation (co-IP) and in situ proximity ligation assay (PLA) to identify Brahma Related Gene 1 (BRG1), the ATP-driven motor of the human SWI-SNF chromatin remodeling complex, as another SAF-A interaction partner in mouse embryonic stem (mES) cells. We also employ RNA interference to investigate functional aspects of the SAF-A/BRG1 interaction. PRINCIPAL FINDINGS: We find that endogenous SAF-A protein interacts with endogenous BRG1 protein in mES cells, and that the interaction does not solely depend on the presence of mRNA. Moreover the interaction remains intact when cells are induced to differentiate. Functional analyses reveal that dual depletion of SAF-A and BRG1 abolishes global transcription by RNA polymerase II, while the nucleolar RNA polymerase I transcription machinery remains unaffected. CONCLUSIONS: We demonstrate that SAF-A interacts with BRG1 and that both components are required for RNA Polymerase II Mediated Transcription.
Databáze: OpenAIRE