Senescent cells assemble specialized structures called senescence-associated heterochromatic foci (SAHF). Heterochromatin is considered to be transcriptionally inactive, and SAHF contain genes associated with cell growth that are essentially switched off. "It seems likely that incorporation of proliferation-associated genes into heterochromatin could contribute to the irreversible cell cycle arrest characteristic of senescence. We are interested in defining the molecular events leading to these changes in chromatin structure in senescent cells," explains study leader Dr. Peter D. Adams from the Fox Chase Cancer Center in Philadelphia.
Dr. Adams and colleagues found that the histone macroH2A is specifically enriched in SAHF. Histones are proteins that are associated with chromatin structure. The researchers also demonstrated that HIRA and ASF1a, two known regulators of chromatin structure, play a key role in formation of SAHF. When human cells were genetically manipulated to activate HIRA and ASF1a, the cells assembled SAHF and showed markers for senescence. If ASF1a was reduced, there was a profound decrease in the number of cells with macroH2A-containing SAHF. These data link changes in cell proliferation to alterations in chromatin structure.
"Together, these observations show that ASF1a promotes and is required for efficient senescence-associated cell cycle exit and support the notion that HIRA/ASF1a-mediated formation of SAHF directly contribute
Contact: Heidi Hardman