Functional interaction between PML and SATB1 regulates chromatin-loop architecture and transcription of the MHC class I locus.

Article Details

Citation

Kumar PP, Bischof O, Purbey PK, Notani D, Urlaub H, Dejean A, Galande S

Functional interaction between PML and SATB1 regulates chromatin-loop architecture and transcription of the MHC class I locus.

Nat Cell Biol. 2007 Jan;9(1):45-56. Epub 2006 Dec 17.

PubMed ID
17173041 [ View in PubMed
]
Abstract

The function of the subnuclear structure the promyelocytic leukaemia (PML) body is unclear largely because of the functional heterogeneity of its constituents. Here, we provide the evidence for a direct link between PML, higher-order chromatin organization and gene regulation. We show that PML physically and functionally interacts with the matrix attachment region (MAR)-binding protein, special AT-rich sequence binding protein 1 (SATB1) to organize the major histocompatibility complex (MHC) class I locus into distinct higher-order chromatin-loop structures. Interferon gamma (IFNgamma) treatment and silencing of either SATB1 or PML dynamically alter chromatin architecture, thus affecting the expression profile of a subset of MHC class I genes. Our studies identify PML and SATB1 as a regulatory complex that governs transcription by orchestrating dynamic chromatin-loop architecture.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Protein PMLP29590Details