KAP1 targets actively transcribed genomic loci to exert pleomorphic effects on RNA polymerase II activity
Author(s) -
Annamaria Kauzlaric,
Suk Min Jang,
Mehdi Morchikh,
Marco Cassano,
Evarist Planet,
Monsef Benkirane,
Didier Trono
Publication year - 2020
Publication title -
philosophical transactions of the royal society b biological sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.753
H-Index - 272
eISSN - 1471-2970
pISSN - 0962-8436
DOI - 10.1098/rstb.2019.0334
Subject(s) - biology , chromatin , rna polymerase ii , transposable element , genetics , transcription (linguistics) , repressor , heterochromatin , promoter , gene , polymerase , microbiology and biotechnology , gene expression , genome , linguistics , philosophy
KAP1 (KRAB-associated protein 1) is best known as a co-repressor responsible for inducing heterochromatin formation, notably at transposable elements. However, it has also been observed to bind the transcription start site of actively expressed genes. To address this paradox, we characterized the protein interactome of KAP1 in the human K562 erythro-leukaemia cell line. We found that the regulator can associate with a wide range of nucleic acid binding proteins, nucleosome remodellers, chromatin modifiers and other transcription modulators. We further determined that KAP1 is recruited at actively transcribed polymerase II promoters, where its depletion resulted in pleomorphic effects, whether expression of these genes was normally constitutive or inducible, consistent with the breadth of possible KAP1 interactors. This article is part of a discussion meeting issue ‘Crossroads between transposons and gene regulation’.
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