replaced
February 20th, 2019 at 3:40am
Note: Replaced Biorxiv
Overview
Abstract
Pathogenic mutations in A-type nuclear lamins cause dilated cardiomyopathy, which is postulated to result from dysregulated gene expression due to changes in chromatin organization into active and inactive compartments. To test this, we performed genome-wide chromosome conformation analyses (Hi-C) in human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) with a haploinsufficient mutation for lamin A/C. Compared to gene-corrected cells, mutant hiPSC-CMs have marked electrophysiological and contractile alterations, with modest gene expression changes. While large-scale changes in chromosomal topology are evident, differences in chromatin compartmentalization are limited to a few hotspots that escape inactivation during cardiogenesis. These regions exhibit upregulation of multiple non-cardiac genes including CACNA1A, encoding for neuronal P/Q-type calcium channels. Pharmacological inhibition of the resulting current partially mitigates the electrical alterations. On the other hand, A/B compartment changes do not explain most gene expression alterations in mutant hiPSC-CMs. We conclude that global errors in chromosomal compartmentation are not the primary pathogenic mechanism in heart failure due to lamin A/C haploinsufficiency.
Authors
Alessandro Bertero • Paul A Fields • Alec ST Smith • Andrea Leonard • Kevin Beussman • Nathan J Sniadecki • Deok-Ho Kim • Hung-Fat Tse • Lil Pabon • Jay Shendure • William S Noble • Charles E Murry
Link
Journal
bioRxiv
doi:10.1101/555250
Published
February 19th, 2019