University of Delhi.
National Institute of Immunology, Delhi.
Epigenetics. 2010 Apr;5(3):241-8. doi: 10.4161/epi.5.3.11417. Epub 2010 Apr 1.
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.
CGG 三核苷酸重复序列中及周围的 CpG 序列的甲基化与脆性 X 综合征在人类患者中的表现有很强的相关性。相比之下,我们在三个不同的携带不稳定 CGG 重复序列的转基因小鼠模型中观察到重复不稳定与 DNA 甲基化之间缺乏相关性。此外,我们还证明了雄性和雌性小鼠的内源性 Fmr1 基因仍然没有被甲基化。这些结果表明甲基化和重复不稳定是独立的事件,并提出了在没有重复扩展的情况下,甲基化也可能导致 FMR1 转录抑制的可能性。