| Literature DB >> 31955845 |
Sandra Catania1, Phillip A Dumesic1, Harold Pimentel2, Ammar Nasif3, Caitlin I Stoddard1, Jordan E Burke1, Jolene K Diedrich4, Sophie Cook1, Terrance Shea5, Elizabeth Geinger5, Robert Lintner5, John R Yates4, Petra Hajkova3, Geeta J Narlikar1, Christina A Cuomo5, Jonathan K Pritchard6, Hiten D Madhani7.
Abstract
Cytosine methylation of DNA is a widespread modification of DNA that plays numerous critical roles. In the yeast Cryptococcus neoformans, CG methylation occurs in transposon-rich repeats and requires the DNA methyltransferase Dnmt5. We show that Dnmt5 displays exquisite maintenance-type specificity in vitro and in vivo and utilizes similar in vivo cofactors as the metazoan maintenance methylase Dnmt1. Remarkably, phylogenetic and functional analysis revealed that the ancestral species lost the gene for a de novo methylase, DnmtX, between 50-150 mya. We examined how methylation has persisted since the ancient loss of DnmtX. Experimental and comparative studies reveal efficient replication of methylation patterns in C. neoformans, rare stochastic methylation loss and gain events, and the action of natural selection. We propose that an epigenome has been propagated for >50 million years through a process analogous to Darwinian evolution of the genome.Entities:
Keywords: Cryptocococcus neoformans; DNA methylation; chromatin; epigenetic memory; epigenetics; evolution; transposable elements
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Year: 2020 PMID: 31955845 PMCID: PMC7197499 DOI: 10.1016/j.cell.2019.12.012
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582