Requirement of <i>CHROMOMETHYLASE3</i> for Maintenance of CpXpG Methylation

Anders M. Lindroth(University of California, Los Angeles), Xiaofeng Cao(University of California, Los Angeles), James P. Jackson(University of California, Los Angeles), Daniel Zilberman(University of California, Los Angeles), Claire M. McCallum(Fred Hutch Cancer Center), Steven Henikoff(Howard Hughes Medical Institute), Steven E. Jacobsen(University of California, Los Angeles)
Science
June 15, 2001
Cited by 946Open Access
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Abstract

Epigenetic silenced alleles of the Arabidopsis SUPERMAN locus (the clark kent alleles) are associated with dense hypermethylation at noncanonical cytosines (CpXpG and asymmetric sites, where X = A, T, C, or G). A genetic screen for suppressors of a hypermethylated clark kent mutant identified nine loss-of-function alleles of CHROMOMETHYLASE3 (CMT3), a novel cytosine methyltransferase homolog. These cmt3 mutants display a wild-type morphology but exhibit decreased CpXpG methylation of the SUP gene and of other sequences throughout the genome. They also show reactivated expression of endogenous retrotransposon sequences. These results show that a non-CpG DNA methyltransferase is responsible for maintaining epigenetic gene silencing.


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