Non-pathogenic microbiota accelerate age-related CpG Island methylation in colonic mucosa

被引:2
|
作者
Sun, Ang [1 ]
Park, Pyoung Hwa [1 ,2 ,5 ]
Cole, Lauren [1 ]
Vaidya, Himani [1 ,2 ]
Maegawa, Shinji [1 ,3 ]
Keith, Kelsey [1 ,2 ]
Calendo, Gennaro [2 ]
Madzo, Jozef [1 ,2 ]
Jelinek, Jaroslav [1 ,2 ]
Jobin, Christian [4 ]
Issa, Jean-Pierre J. [1 ,2 ,6 ]
机构
[1] Temple Univ, Fels Canc Inst Personalized Med, Sch Med, Philadelphia, PA USA
[2] Coriell Inst Med Res, Camden, NJ USA
[3] Univ Texas MD Anderson Canc Ctr, Res Dept Pediat, Houston, TX USA
[4] Dept Med, Div Gastroenterol Hepatol & Nutr, Houston, TX USA
[5] Coriell Inst Med Res, Fels Canc Inst Personalized Med, Camden, NJ 08103 USA
[6] Coriell Inst Med Res, 403 Haddon Ave, Camden, NJ 08103 USA
基金
美国国家卫生研究院;
关键词
DNA methylation; Microbiota; Germ-free; Inflammation; Ageing; ABERRANT DNA METHYLATION; HELICOBACTER-PYLORI; EPIGENETIC DRIFT; CANCER; PHENOTYPE; DIET; HYPERMETHYLATION; ASSOCIATION; MUTATIONS; INFECTION;
D O I
10.1080/15592294.2022.2160568
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA methylation is an epigenetic process altered in cancer and ageing. Age-related methylation drift can be used to estimate lifespan and can be influenced by extrinsic factors such as diet. Here, we report that non-pathogenic microbiota accelerate age-related methylation drift in the colon when compared with germ-free mice. DNA methylation analyses showed that microbiota and IL10KO were associated with changes in 5% and 4.1% of CpG sites, while mice with both factors had 18% alterations. Microbiota, IL10KO, and their combination altered 0.4%, 0.4%, and 4% of CpG island methylation, respectively. These are comparable to what is seen in colon cancer. Ageing changes were accelerated in the IL10KO mice with microbiota, and the affected genes were more likely to be altered in colon cancer. Thus, the microbiota affect DNA methylation of the colon in patterns reminiscent of what is observed in ageing and colorectal cancer.
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页数:14
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