Comparative analysis of DNA methylation in transgenic mice with unstable CGG repeats from FMR1 gene

被引:5
|
作者
Alam, Mohammad Parwez [1 ]
Datta, Sonal [1 ]
Majumdar, Subeer [2 ]
Mehta, Abhishek K. [1 ]
Baskaran, Sujatha [1 ]
Gulati, Neerja [2 ]
Brahmachari, Vani [1 ]
机构
[1] Univ Delhi, Dr BR Ambedkar Ctr Biomed Res, Delhi 110007, India
[2] Natl Inst Immunol, Delhi, India
关键词
DNA methylation; CGG repeat instability; transgenic mice; mouse Fmr1 methylation; McrBC-HpaII; bisulfite sequencing; unclassified MR patients; FRAGILE-X-SYNDROME; FULL MUTATION; ABNORMAL METHYLATION; PROTEIN EXPRESSION; I LOCUS; INSTABILITY; MALES; PREMUTATION; PHENOTYPE; POSTMORTEM;
D O I
10.4161/epi.5.3.11417
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
Methylation of CpG sequences in and around CGG triplet repeats in FMR1 gene has strong correlation with manifestation of the fragile X syndrome in human patients. In contrast, we have observed a lack of correlation between repeat instability and DNA methylation in three different transgenic mouse models harboring unstable CGG repeats. Further we have demonstrated that the endogenous copy of mouse Fmr1 gene remains unmethylated both in males and females. These results imply that methylation and repeat instability are independent events and raise the possibility that methylation could also result in repression of FMR1 transcription in the absence of repeat expansion.
引用
收藏
页码:241 / 248
页数:8
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