Miyazaki Kazumi, Mapendano Christophe K, Fuchigami Tomokazu, Kondo Shinji, Ohta Tohru, Kinoshita Akira, Tsukamoto Kazuhiro, Yoshiura Ko-ichiro, Niikawa Norio, Kishino Tatsuya
Division of Functional Genomics, Center for Frontier Life Sciences, Nagasaki University, Sakamoto 1-12-4, Nagasaki 852-8523, Japan.
Gene. 2009 Mar 1;432(1-2):97-101. doi: 10.1016/j.gene.2008.11.019. Epub 2008 Nov 27.
The mouse Snurf/Snrpn gene has two differentially methylated regions (DMRs), the maternally methylated region at the 5' end (DMR1) and the paternally methylated region at the 3' end (DMR2). DMR1, a region that includes the Snrpn promoter and the entire intron 1, has been thought to be a germline DMR, which inherits the parental-specific methylation profile from the gametes. DMR1 is not only associated with imprinted Snrpn expression, but implicated in imprinting control of other genes in the region. We have now characterized the highly conserved activator sequence (CAS) in the Snrpn intron 1 among human and rodents and demonstrate that the mouse CAS is not a germline DMR but shows developmentally dynamic changes of DNA methylation and has methylation-sensitive enhancer activity. The tissue-specific methylation of the mouse CAS and its methylation-sensitive enhancer activity may control tissue-specific expression of IC transcripts, resulting in the establishment and/or maintenance of imprinting in the Snrpn locus.
小鼠的Snurf/Snrpn基因有两个差异甲基化区域(DMR),即5'端的母源甲基化区域(DMR1)和3'端的父源甲基化区域(DMR2)。DMR1区域包含Snrpn启动子和整个内含子1,一直被认为是种系DMR,它从配子中继承亲本特异性甲基化模式。DMR1不仅与印记基因Snrpn的表达相关,还参与该区域其他基因的印记控制。我们现已对人和啮齿动物Snrpn内含子1中高度保守的激活序列(CAS)进行了表征,并证明小鼠的CAS不是种系DMR,而是呈现出DNA甲基化的发育动态变化且具有甲基化敏感增强子活性。小鼠CAS的组织特异性甲基化及其甲基化敏感增强子活性可能控制IC转录本的组织特异性表达,从而导致Snrpn基因座印记的建立和/或维持。