Genome methylation in D. melanogaster is found at specific short motifs and is independent of DNMT2 activity

  1. Dario Boffelli1,3
  1. 1 Children's Hospital Oakland Research Institute;
  2. 2 UC Berkeley
  1. * Corresponding author; email: dboffelli{at}chori.org

Abstract

Cytosine methylation in the genome of Drosophila melanogaster has been elusive and controversial: its location and function have not been established. We have used a novel and highly sensitive genome-wide cytosine methylation assay to detect and map genome methylation in Stage 5 Drosophila embryos. The methylation we observe with this method is highly localized and strand-asymmetrical, limited to regions covering ~1% of the genome, dynamic in early embryogenesis, and concentrated in specific 5-base sequence motifs that are CA- and CT-rich but depleted of guanine. Gene body methylation is associated with lower expression, and many genes containing methylated regions have developmental or transcriptional functions. The only known DNA methyltransferase in Drosophila is DNMT2, but lines deficient for DNMT2 retain genomic methylation, implying the presence of a novel methyltransferase. The association of methylation with lower expression of specific developmental genes at Stage 5 raises the possibility that it participates in controlling gene expression during the maternal-zygotic transition.

  • Received June 21, 2013.
  • Accepted February 18, 2014.

This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported), as described at http://creativecommons.org/licenses/by-nc/3.0/.

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  1. Genome Res. gr.162412.113 Published by Cold Spring Harbor Laboratory Press

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