Dnmt3a-Dependent Nonpromoter DNA Methylation Facilitates Transcription of Neurogenic Genes

Author:

Wu Hao1,Coskun Volkan2,Tao Jifang2,Xie Wei3,Ge Weihong1,Yoshikawa Kazuaki4,Li En5,Zhang Yi6,Sun Yi Eve12

Affiliation:

1. Department of Molecular and Medical Pharmacology, University of California Los Angeles (UCLA), Los Angeles, CA 90095, USA.

2. Department of Psychiatry and Biobehavioral Sciences, Intellectual Development and Disabilities Research Center at Semel Institute for Neuroscience, UCLA, Los Angeles, CA 90095, USA.

3. Molecular Biology Institute, UCLA School of Medicine, Los Angeles, CA 90095, USA.

4. Laboratory of Regulation of Neuronal Development, Institute for Protein Research, Osaka University, Suita, Osaka, 565-0871, Japan.

5. Novartis Institutes for Biomedical Research, Cambridge, MA 02139, USA.

6. Howard Hughes Medical Institute, Department of Biochemistry and Biophysics, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Abstract

Location, Location, Location The genome receives epigenetic marks throughout development that regulate the activity of multiple genes. One such mark is methylation, which usually represses gene transcription. Methylation has generally been studied in the promoters of genes, where many regulatory signals coordinate to control the expression of the gene. Studying neural stem cells from mice, Wu et al. (p. 444 ) now show that DNA methylation can be a double-edged sword. Although methylation of DNA sequences in promoters tends to be repressive, methylation of DNA sequences beyond the promoters can actually promote gene expression. Analysis of the methyltransferase Dnmt3a in mouse neural stem cells revealed that methylations around neurogenic genes—but outside their promoters—maintained the activity of these genes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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