Persistent nuclear actin filaments inhibit transcription by RNA polymerase II

Author:

Serebryannyy Leonid A.1,Parilla Megan1,Annibale Paolo2ORCID,Cruz Christina M.1,Laster Kyle3,Gratton Enrico2ORCID,Kudryashov Dmitri4,Kosak Steven T.3,Gottardi Cara J.5ORCID,de Lanerolle Primal1ORCID

Affiliation:

1. Department of Physiology and Biophysics, University of Illinois at Chicago, Chicago, IL, USA

2. Laboratory of Fluorescence Dynamics, University of California Irvine, Irvine, CA, USA

3. Department of Cell and Molecular Biology, Northwestern University, Chicago, IL, USA

4. Department of Chemistry and Biochemistry, Ohio State University, Columbus, OH, USA

5. Department of Medicine, Northwestern University, Chicago, IL, USA

Abstract

Actin is abundant in the nucleus and it is clear that nuclear actin has important functions. Yet, 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.

Funder

National Institute of General Medical Sciences

American Heart Association

National Cancer Institute

Chicago Community Trust

University of Illinois at Chicago

Publisher

The Company of Biologists

Subject

Cell Biology

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