Heritable gene silencing in lymphocytes delays chromatid resolution without affecting the timing of DNA replication View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2003-06-29

AUTHORS

Véronique Azuara, Karen E. Brown, Ruth R. E. Williams, Natasha Webb, Niall Dillon, Richard Festenstein, Veronica Buckle, Matthias Merkenschlager, Amanda G. Fisher

ABSTRACT

Temporal control of DNA replication has been implicated in epigenetic regulation of gene expression on the basis of observations that certain tissue-specific genes replicate earlier in expressing than non-expressing cells. Here, we show evidence that several leukocyte-specific genes replicate early in lymphocytes regardless of their transcription and also in fibroblasts, where these genes are never normally expressed. Instead, the heritable silencing of some genes (Rag-1, TdT, CD8α and λ5) and their spatial recruitment to heterochromatin domains within the nucleus of lymphocytes resulted in a markedly delayed resolution of sister chromatids into doublet signals discernable by 3D fluorescence in situ hybridization (FISH). Integration of transgenes within heterochromatin (in cis) did, however, confer late replication and this was reversed after variegated transgene expression. These findings emphasise that chromosomal location is important for defining the replication timing of genes and show that retarded sister-chromatid resolution is a novel feature of inactive chromatin. More... »

PAGES

668-674

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/ncb1006

DOI

http://dx.doi.org/10.1038/ncb1006

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1050069262

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/12833066


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