| Literature DB >> 30459231 |
Maria Michela Marino1, Camilla Rega1, Rosita Russo1, Mariangela Valletta1, Maria Teresa Gentile1, Sabrina Esposito1, Ilaria Baglivo1, Italia De Feis2, Claudia Angelini2, Tioajiang Xiao3, Gary Felsenfeld3, Angela Chambery4, Paolo Vincenzo Pedone5.
Abstract
The highly conserved zinc finger CCCTC-binding factor (CTCF) regulates genomic imprinting and gene expression by acting as a transcriptional activator or repressor of promoters and insulator of enhancers. The multiple functions of CTCF are accomplished by co-association with other protein partners and are dependent on genomic context and tissue specificity. Despite the critical role of CTCF in the organization of genome structure, to date, only a subset of CTCF interaction partners have been identified. Here we present a large-scale identification of CTCF-binding partners using affinity purification and high-resolution LC-MS/MS analysis. In addition to functional enrichment of specific protein families such as the ribosomal proteins and the DEAD box helicases, we identified novel high-confidence CTCF interactors that provide a still unexplored biochemical context for CTCF's multiple functions. One of the newly validated CTCF interactors is BRG1, the major ATPase subunit of the chromatin remodeling complex SWI/SNF, establishing a relationship between two master regulators of genome organization. This work significantly expands the current knowledge of the human CTCF interactome and represents an important resource to direct future studies aimed at uncovering molecular mechanisms modulating CTCF pleiotropic functions throughout the genome.Entities:
Keywords: BRG1; CTCF; Interactomics; SWI/SNF; chromatin; mass spectrometry (MS); protein–protein interaction; proteomics; transcription factor; transcriptional regulation
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Year: 2018 PMID: 30459231 PMCID: PMC6341399 DOI: 10.1074/jbc.RA118.004882
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157