Department of Cell and Developmental Biology; Nickerson Lab
Biochemistry, Biophysics, and Structural Biology | Cell Biology
Mechanical integration of the nucleus with the extracellular matrix (ECM) is established by linkage between the cytoskeleton and the nucleus. This integration is hypothesized to mediate sensing of ECM rigidity, but parsing the function of nucleus-cytoskeleton linkage from other mechanisms has remained a central challenge. Here we took advantage of the fact that the LINC (linker of nucleoskeleton and cytoskeleton) complex is a known molecular linker of the nucleus to the cytoskeleton, and asked how it regulates the sensitivity of genome-wide transcription to substratum rigidity. We show that gene mechanosensitivity is preserved after LINC disruption, but reversed in direction. Combined with myosin inhibition studies, we identify genes that depend on nuclear tension for their regulation. We also show that LINC disruption does not attenuate nuclear shape sensitivity to substrate rigidity. Our results show for the first time that the LINC complex facilitates mechano-regulation of expression across the genome.
Biophysics, Gene expression
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Copyright © 2016, The Author(s).
DOI of Published Version
Sci Rep. 2016 Dec 1;6:38063. doi: 10.1038/srep38063. Link to article on publisher's site
Alam SG, Zhang Q, Prasad N, Li Y, Chamala S, Kuchibhotla R, Kc B, Aggarwal V, Shrestha S, Jones AL, Levy SE, Roux KJ, Nickerson JA, Lele TP. (2016). The mammalian LINC complex regulates genome transcriptional responses to substrate rigidity. Open Access Articles. https://doi.org/10.1038/srep38063. Retrieved from https://escholarship.umassmed.edu/oapubs/3030
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