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.
Sean P. Cregan, Andre Fortin, Jason G. MacLaurin, Steven M. Callaghan, Francesco Cecconi, Seong-Woon Yu, Ted M. Dawson, Valina L. Dawson, David S. Park, Guido Guido Kroemer, Ruth S. Slack
Discussion(0)
No comments yet. Be the first to comment.