| Literature DB >> 34106828 |
Amy R Strom1, Ronald J Biggs2, Edward J Banigan3, Xiaotao Wang4, Katherine Chiu5, Cameron Herman2, Jimena Collado2, Feng Yue4,6, Joan C Ritland Politz7, Leah J Tait7, David Scalzo7, Agnes Telling7, Mark Groudine7, Clifford P Brangwynne1, John F Marko2,8, Andrew D Stephens5.
Abstract
Chromatin, which consists of DNA and associated proteins, contains genetic information and is a mechanical component of the nucleus. Heterochromatic histone methylation controls nucleus and chromosome stiffness, but the contribution of heterochromatin protein HP1α (CBX5) is unknown. We used a novel HP1α auxin-inducible degron human cell line to rapidly degrade HP1α. Degradation did not alter transcription, local chromatin compaction, or histone methylation, but did decrease chromatin stiffness. Single-nucleus micromanipulation reveals that HP1α is essential to chromatin-based mechanics and maintains nuclear morphology, separate from histone methylation. Further experiments with dimerization-deficient HP1αI165E indicate that chromatin crosslinking via HP1α dimerization is critical, while polymer simulations demonstrate the importance of chromatin-chromatin crosslinkers in mechanics. In mitotic chromosomes, HP1α similarly bolsters stiffness while aiding in mitotic alignment and faithful segregation. HP1α is therefore a critical chromatin-crosslinking protein that provides mechanical strength to chromosomes and the nucleus throughout the cell cycle and supports cellular functions.Entities:
Keywords: HP1a; cell biology; chromosome; chromosomes; gene expression; heterochromatin; human; mechanics; mitosis; nucleus
Mesh:
Substances:
Year: 2021 PMID: 34106828 PMCID: PMC8233041 DOI: 10.7554/eLife.63972
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.713