Cargando…
H4K20 methylation regulates quiescence and chromatin compaction
The transition between proliferation and quiescence is frequently associated with changes in gene expression, extent of chromatin compaction, and histone modifications, but whether changes in chromatin state actually regulate cell cycle exit with quiescence is unclear. We find that primary human fib...
Autores principales: | Evertts, Adam G., Manning, Amity L., Wang, Xin, Dyson, Nicholas J., Garcia, Benjamin A., Coller, Hilary A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784377/ https://www.ncbi.nlm.nih.gov/pubmed/23924899 http://dx.doi.org/10.1091/mbc.E12-07-0529 |
Ejemplares similares
-
A New Description of Cellular Quiescence
por: Coller, Hilary A, et al.
Publicado: (2006) -
Widespread changes in mRNA stability contribute to quiescence-specific gene expression patterns in a fibroblast model of quiescence
por: Johnson, Elizabeth L., et al.
Publicado: (2017) -
Is There a Histone Code for Cellular Quiescence?
por: Bonitto, Kenya, et al.
Publicado: (2021) -
Histone H4K20 methylation mediated chromatin compaction threshold ensures genome integrity by limiting DNA replication licensing
por: Shoaib, Muhammad, et al.
Publicado: (2018) -
Adenovirus type 5 exerts genome-wide control over cellular programs governing proliferation, quiescence, and survival
por: Miller, Daniel L, et al.
Publicado: (2007)