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Persistent nuclear actin filaments inhibit transcription by RNA polymerase II
Author(s) -
Leonid Serebryannyy,
Megan Parilla,
Paolo Annibale,
Christina M. Cruz,
Kyle Vaughn Laster,
Enrico Gratton,
Dmitri S. Kudryashov,
Steven T. Kosak,
Cara J. Gottardi,
Primal de Lanerolle
Publication year - 2016
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.195867
Subject(s) - biology , rna polymerase ii , mdia1 , microbiology and biotechnology , transcription (linguistics) , actin , cell nucleus , actin remodeling , actin cytoskeleton , cytoskeleton , gene expression , biochemistry , nucleus , gene , cell , promoter , linguistics , philosophy
Actin is abundant in the nucleus and it is clear that nuclear actin has important functions. However, mystery surrounds the absence of classical actin filaments in the nucleus. To address this question, we investigated how polymerizing nuclear actin into persistent nuclear actin filaments affected transcription by RNA polymerase II. Nuclear filaments impaired nuclear actin dynamics by polymerizing and sequestering nuclear actin. Polymerizing actin into stable nuclear filaments disrupted the interaction of actin with RNA polymerase II and correlated with impaired RNA polymerase II localization, dynamics, gene recruitment, and reduced global transcription and cell proliferation. Polymerizing and crosslinking nuclear actin in vitro similarly disrupted the actin-RNA-polymerase-II interaction and inhibited transcription. These data rationalize the general absence of stable actin filaments in mammalian somatic nuclei. They also suggest a dynamic pool of nuclear actin is required for the proper localization and activity of RNA polymerase II.

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