Transcription inhibition suppresses nuclear blebbing and rupture independently of nuclear rigidity

Author:

Berg Isabel K.12,Currey Marilena L.1,Gupta Sarthak3,Berrada Yasmin1,Nguyen Bao V.2,Pho Mai1,Patteson Alison E.3ORCID,Schwarz J. M.34,Banigan Edward J.56ORCID,Stephens Andrew D.12ORCID

Affiliation:

1. University of Massachusetts Amherst 1 Biology Department , , Amherst, MA 01003 , USA

2. University of Massachusetts Amherst 2 Molecular and Cellular Biology , , Amherst, MA 01003 , USA

3. Syracuse University 3 Department of Physics and BioInspired Syracuse , , Syracuse, NY 13244 , USA

4. Indian Creek Farm 4 , Ithaca, NY 14850 , USA

5. Institute of Medical Engineering & Science 5 and Department of Physics , , Cambridge, MA 02139 , USA

6. Massachusetts Institute of Technology 5 and Department of Physics , , Cambridge, MA 02139 , USA

Abstract

ABSTRACT Chromatin plays an essential role in the nuclear mechanical response and determining nuclear shape, which maintain nuclear compartmentalization and function. However, major genomic functions, such as transcription activity, might also impact cell nuclear shape via blebbing and rupture through their effects on chromatin structure and dynamics. To test this idea, we inhibited transcription with several RNA polymerase II inhibitors in wild-type cells and perturbed cells that presented increased nuclear blebbing. Transcription inhibition suppressed nuclear blebbing for several cell types, nuclear perturbations and transcription inhibitors. Furthermore, transcription inhibition suppressed nuclear bleb formation, bleb stabilization and bleb-based nuclear ruptures. Interestingly, transcription inhibition did not alter the histone H3 lysine 9 (H3K9) modification state, nuclear rigidity, and actin compression and contraction, which typically control nuclear blebbing. Polymer simulations suggested that RNA polymerase II motor activity within chromatin could drive chromatin motions that deform the nuclear periphery. Our data provide evidence that transcription inhibition suppresses nuclear blebbing and rupture, in a manner separate and distinct from chromatin rigidity.

Funder

National Institutes of Health

National Science Foundation

Syracuse University

Publisher

The Company of Biologists

Subject

Cell Biology

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