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Title: Senescence of nickel-transformed cells by an X chromosome: Possible epigenetic control

Journal Article · · Science (Washington, D.C.); (United States)
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  1. New York Univ. Medical Center, NY (United States)
  2. Univ. of North Carolina Medical School, Chapel Hill (United States)
  3. National Inst. of Environmental Health Sciences, Research Triangle Park, NC (United States)

Transfer of a normal Chinese hamster X chromosome (carried in a mouse A9 donor cell line) to a nickel-transformed Chinese hamster cell line with an Xq chromosome deletion resulted in senescense of these previously immortal cells. At early passages of the A9/CX donor cells, the hamster X chromosome was highly active, inducing senescence in 100% of the colonies obtained after its transfer into the nickel-transformed cells. However, senescence was reduced to 50% when Chinese hamster X chromosomes were transferred from later passage A9 cells. Full senescing activity of the intact hamster X chromosome was restored by treatment of the donor mouse cells with 5-azacytidine, which induced demethylation of DMA. These results suggest that a senescence gene or genes, which may be located on the Chinese hamster X chromosome, can be regulated by DNA methylation, and that escape from senescence and possibly loss of tumor suppressor gene activity can occur by epigenetic mechanisms.

OSTI ID:
5596855
Journal Information:
Science (Washington, D.C.); (United States), Vol. 251:4995; ISSN 0036-8075
Country of Publication:
United States
Language:
English