Редактирование: MCHR1

Melanin-concentrating hormone receptor 1 (MCH receptor 1) (MCH-R1) (MCHR-1) (G-protein coupled receptor 24) (MCH-1R) (MCH1R) (MCHR) (SLC-1) (Somatostatin receptor-like protein) [GPR24] [SLC1]

==Publications==

{{medline-entry
|title=Allele-specific, age-dependent and BMI-associated DNA methylation of human [[MCHR1]].
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/21637341
|abstract=Melanin-concentrating hormone receptor 1 ([[MCHR1]]) plays a significant role in regulation of energy balance, food intake, physical activity and body weight in humans and rodents. Several association studies for human obesity showed contrary results concerning the SNPs rs133072 (G/A) and rs133073 (T/C), which localize to the first exon of [[MCHR1]]. The variations constitute two main haplotypes (GT, AC). Both SNPs affect CpG dinucleotides, whereby each haplotype contains a potential methylation site at one of the two SNP positions. In addition, 15 CpGs in close vicinity of these SNPs constitute a weak CpG island. Here, we studied whether DNA methylation in this sequence context may contribute to population- and age-specific effects of [[MCHR1]] alleles in obesity. We analyzed DNA methylation of a 315 bp region of [[MCHR1]] encompassing rs133072 and rs133073 and the CpG island in blood samples of 49 individuals by bisulfite sequencing. The AC haplotype shows a significantly higher methylation level than the GT haplotype. This allele-specific methylation is age-dependent. In young individuals (20-30 years) the difference in DNA methylation between haplotypes is significant; whereas in individuals older than 60 years it is not detectable. Interestingly, the GT allele shows a decrease in methylation status with increasing BMI, whereas the methylation of the AC allele is not associated with this phenotype. Heterozygous lymphoblastoid cell lines show the same pattern of allele-specific DNA methylation. The cell line, which exhibits the highest difference in methylation levels between both haplotypes, also shows allele-specific transcription of [[MCHR1]], which can be abolished by treatment with the DNA methylase inhibitor 5-aza-2'-deoxycytidine. We show that DNA methylation at [[MCHR1]] is allele-specific, age-dependent, BMI-associated and affects transcription. Conceivably, this epigenetic regulation contributes to the age- and/or population specific effects reported for [[MCHR1]] in several human obesity studies.
|mesh-terms=* Adult
* Aged
* Aging
* Alleles
* Azacitidine
* Body Mass Index
* Cell Line
* CpG Islands
* DNA Methylation
* Gene Expression Regulation
* Genome, Human
* Humans
* Male
* Middle Aged
* RNA, Messenger
* Receptors, Somatostatin
* Young Adult

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102661
}}