| Literature DB >> 23370394 |
Abstract
A new study shows that the expression of two classes of repetitive elements in the mouse genome is controlled through two complementary mechanisms: DNA methylation and p53-mediated transcription suppression.¹ When both lines of defense fail, expression of the repeats yields large quantities of double-stranded RNA, triggering interferon response that leads to caspase-dependent cell death. These notable findings highlight two fundamental trends: tight coupling of defense and cell death mechanisms that appears to be universal in cellular life and the exploitation of the expression of "junk" DNA as a signal triggering "altruistic" cell suicide.Entities:
Keywords: DNA methylation; SINE repeats; interferon response; p53; transposable elements
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Year: 2013 PMID: 23370394 PMCID: PMC3594256 DOI: 10.4161/cc.23717
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534