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Transcription inhibition suppresses nuclear blebbing and rupture independent of nuclear rigidity.

Isabel K BergMarilena L CurreySarthak GuptaYasmin BerradaBao V NguyenMai PhoAlison E PattesonJ M SchwarzEdward J BaniganAndrew D Stephens
Published in: Journal of cell science (2023)
Chromatin is an essential component of nuclear mechanical response and shape that maintains 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 present increased nuclear blebbing. Transcription inhibition suppresses nuclear blebbing for several cell types, nuclear perturbations, and transcription inhibitors. Furthermore, transcription inhibition suppresses nuclear bleb formation, bleb stabilization, and bleb-based nuclear ruptures. Interestingly, transcription inhibition does not alter either H3K9 histone modification state, nuclear rigidity, or actin compression and contraction, which typically control nuclear blebbing. Polymer simulations suggest that RNA pol 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, separate and distinct from chromatin rigidity.
Keyphrases
  • transcription factor
  • dna damage
  • signaling pathway
  • induced apoptosis
  • genome wide
  • single cell
  • dna methylation
  • cell therapy
  • mesenchymal stem cells
  • copy number
  • cell death
  • smooth muscle
  • pi k akt