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Promoter methylation and age-related downregulation of Klotho in rhesus monkey
被引:76
|作者:
King, Gwendalyn D.
[1
]
Rosene, Douglas L.
[2
,3
]
Abraham, Carmela R.
[1
]
机构:
[1] Boston Univ, Sch Med, Dept Biochem, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Dept Anat & Neurobiol, Boston, MA 02118 USA
[3] Emory Univ, Yerkes Natl Primate Res Ctr, Atlanta, GA 30322 USA
来源:
关键词:
Oxidation;
Methylation;
Age downregulation;
White matter;
Pyrosequencing;
MYELINATED NERVE-FIBERS;
DNA METHYLATION;
WHITE-MATTER;
FUNCTIONAL VARIANT;
EPIGENETIC REGULATION;
PREFRONTAL CORTEX;
ALPHA-KLOTHO;
MUTANT MOUSE;
LIFE-SPAN;
AREA;
46;
D O I:
10.1007/s11357-011-9315-4
中图分类号:
R592 [老年病学];
C [社会科学总论];
学科分类号:
03 ;
0303 ;
100203 ;
摘要:
While overall DNA methylation decreases with age, CpG-rich areas of the genome can become hypermethylated. Hypermethylation near transcription start sites typically decreases gene expression. Klotho (KL) is important in numerous age-associated pathways including insulin/IGF1 and Wnt signaling and naturally decreases with age in brain, heart, and liver across species. Brain tissues from young and old rhesus monkeys were used to determine whether epigenetic modification of the KL promoter underlies age-related decreases in mRNA and protein levels of KL. The KL promoter in genomic DNA from brain white matter did not show evidence of oxidation in vivo but did exhibit an increase in methylation with age. Further analysis identified individual CpG motifs across the region of interest with increased methylation in old animals. In vitro methyl modification of these individual cytosine residues confirmed that methylation of the promoter can decrease gene transcription. These results provide evidence that changes in KL gene expression with age may, at least in part, be the result of epigenetic changes to the 5' regulatory region.
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页码:1405 / 1419
页数:15
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