Journal
JOURNAL OF NEUROSCIENCE
Volume 33, Issue 50, Pages 19704-19714Publisher
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.2355-13.2013
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Funding
- project Highly Creative Animal Model Development for Brain Sciences by the Ministry of Education, Culture, Sports, Science, and Technology of Japan
- Ministry of Education, Culture, Sports, Science, and Technology, of Japan
- Grants-in-Aid for Scientific Research [25640016, 22123009] Funding Source: KAKEN
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Distinct anatomical regions of the neocortex subserve different sensory modalities and neuronal integration functions, but mechanisms for these regional specializations remain elusive. Involvement of epigenetic mechanisms for such specialization through the spatiotemporal regulation of gene expression is an intriguing possibility. Here we examined whether epigenetic mechanisms might play a role in the selective gene expression in the association areas (AAs) and the primary visual cortex (V1) in macaque neocortex. By analyzing the two types of area-selective gene promoters that we previously identified, we found a striking difference of DNA methylation between these promoters, i.e., hypermethylation in AA-selective gene promoters and hypomethylation in V1-selective ones. Methylation levels of promoters of each area-selective gene showed no areal difference, but a specific methyl-binding protein (MBD4) was enriched in the AAs, in correspondence with expression patterns of AA-selective genes. MBD4 expression was mainly observed in neurons. MBD4 specifically bound to and activated the AA-selective genes both in vitro and in vivo. Our results demonstrate that methylation in the promoters and specific methyl-binding proteins play an important role in the area-selective gene expression profiles in the primate neocortex.
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