Epigenetic differences between sister chromatids?

Author: Lansdorp PM, Falconer E, Tao J, Brind'amour J, Naumann U.
Affiliation:
Terry Fox Laboratory, BC Cancer Agency, Vancouver, British Columbia, Canada. Division of Hematology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada. European Research Institute for the Biology of Ageing, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Conference/Journal: Ann N Y Acad Sci.
Date published: 2012 Aug
Other: Volume ID: 1266 , Issue ID: 1 , Pages: 1-6 , Special Notes: doi: 10.1111/j.1749-6632.2012.06505.x. , Word Count: 189



Semi-conservative replication ensures that the DNA sequence of sister chromatids is identical except for replication errors and variation in the length of telomere repeats resulting from replicative losses and variable end processing. What happens with the various epigenetic marks during DNA replication is less clear. Many chromatin marks are likely to be copied onto both sister chromatids in conjunction with DNA replication, whereas others could be distributed randomly between sister chromatids. Epigenetic differences between sister chromatids could also emerge in a more predictable manner, for example, following processes that are associated with lagging strand DNA replication. The resulting epigenetic differences between sister chromatids could result in different gene expression patterns in daughter cells. This possibility has been difficult to test because techniques to distinguish between parental sister chromatids require analysis of single cells and are not obvious. Here, we briefly review the topic of sister chromatid epigenetics and discuss how the identification of sister chromatids in cells could change the way we think about asymmetric cell divisions and stochastic variation in gene expression between cells in general and paired daughter cells in particular.
© 2012 New York Academy of Sciences.
PMID: 22901250

BACK