TY - JOUR
T1 - Effects of forces on chromatin
AU - Amar, Kshitij
AU - Wei, Fuxiang
AU - Chen, Junwei
AU - Wang, Ning
N1 - Funding Information:
We thank lab members (current and former) and collaborators for our published work cited in this review. Due to space limitation, we are not able to list all relevant publications in this topic. The authors acknowledge support from NIH under Grant No. GM072744 and Hoeft Professorship of University of Illinois at Urbana-Champaign (N.W.); NSFC under Grant No. 11902122 (F.W.); and NSFC under Grant Nos. 11902121 and 32071306 (J.C.).
Publisher Copyright:
© 2021 Author(s).
PY - 2021/12/1
Y1 - 2021/12/1
N2 - Chromatin is a unique structure of DNA and histone proteins in the cell nucleus and the site of dynamic regulation of gene expression. Soluble factors are known to affect the chromatin structure and function via activating or inhibiting specific transcription factors. Forces on chromatin come from exogenous stresses on the cell surface and/or endogenous stresses, which are regulated by substrate mechanics, geometry, and topology. Forces on chromatin involve direct (via adhesion molecules, cytoskeleton, and the linker of nucleoskeleton and cytoskeleton complexes) and indirect (via diffusion and/or translocation processes) signaling pathways to modulate levels of chromatin folding and deformation to regulate transcription, which is controlled by histone modifications and depends on magnitude, direction, rate/frequency, duration, and modes of stresses. The rapid force transmission pathway activates multiple genes simultaneously, and the force may act like a “supertranscription factor.” The indirect mechanotransduction pathways and the rapid force transmission pathway together exert sustained impacts on the chromatin, the nucleus, and cell functions.
AB - Chromatin is a unique structure of DNA and histone proteins in the cell nucleus and the site of dynamic regulation of gene expression. Soluble factors are known to affect the chromatin structure and function via activating or inhibiting specific transcription factors. Forces on chromatin come from exogenous stresses on the cell surface and/or endogenous stresses, which are regulated by substrate mechanics, geometry, and topology. Forces on chromatin involve direct (via adhesion molecules, cytoskeleton, and the linker of nucleoskeleton and cytoskeleton complexes) and indirect (via diffusion and/or translocation processes) signaling pathways to modulate levels of chromatin folding and deformation to regulate transcription, which is controlled by histone modifications and depends on magnitude, direction, rate/frequency, duration, and modes of stresses. The rapid force transmission pathway activates multiple genes simultaneously, and the force may act like a “supertranscription factor.” The indirect mechanotransduction pathways and the rapid force transmission pathway together exert sustained impacts on the chromatin, the nucleus, and cell functions.
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U2 - 10.1063/5.0065302
DO - 10.1063/5.0065302
M3 - Review article
C2 - 34661040
AN - SCOPUS:85117194188
SN - 2473-2877
VL - 5
JO - APL Bioengineering
JF - APL Bioengineering
IS - 4
M1 - 041503
ER -