Goodfellow P J, Mondello C, Darling S M, Pym B, Little P, Goodfellow P N
Human Molecular Genetics Laboratory, Imperial Cancer Research Fund, London, England.
Proc Natl Acad Sci U S A. 1988 Aug;85(15):5605-9. doi: 10.1073/pnas.85.15.5605.
We have identified and characterized a Hpa II tiny fragment (HTF) island associated with the promoter region of the pseudoautosomal gene MIC2. The MIC2 HTF island is unmethylated on both the active and inactive X chromosome and is similarly unmethylated on the Y chromosome. Unlike the majority of genes borne on the X chromosome, MIC2 fails to undergo X chromosome inactivation. HTF islands associated with X chromosome-linked genes that are inactivated are highly methylated on the inactive or transcriptionally silent homologue. The failure of MIC2 to undergo X chromosome inactivation correlates with the lack of methylation of the HTF island at the 5' end of the gene. These results provide further evidence that DNA methylation plays an important role in the phenomenon of X chromosome inactivation.
我们已经鉴定并表征了一个与假常染色体基因MIC2启动子区域相关的Hpa II微小片段(HTF)岛。MIC2 HTF岛在活性和非活性X染色体上均未甲基化,在Y染色体上同样未甲基化。与大多数位于X染色体上的基因不同,MIC2不会发生X染色体失活。与失活的X染色体连锁基因相关的HTF岛在非活性或转录沉默的同源染色体上高度甲基化。MIC2未能发生X染色体失活与该基因5'端HTF岛缺乏甲基化相关。这些结果进一步证明DNA甲基化在X染色体失活现象中起重要作用。