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由其自身转基因导致的印记基因U2af1-rs1(SP2)的异常甲基化。

Aberrant methylation of an imprinted gene U2af1-rs1(SP2) caused by its own transgene.

作者信息

Hatada I, Nabetani A, Arai Y, Ohishi S, Suzuki M, Miyabara S, Nishimune Y, Mukai T

机构信息

Department of Bioscience, National Cardiovascular Center Research Institute, 5-7-1, Fujishiro-dai, Suita, Osaka 565, Japan.

出版信息

J Biol Chem. 1997 Apr 4;272(14):9120-2. doi: 10.1074/jbc.272.14.9120.

Abstract

Genomic imprinting refers to the parental allele-specific expression of genes. The precise mechanism underlying this phenomenon, which may involve DNA methylation, is not yet known. U2af1-rs1(SP2) is an imprinted gene expressed from the paternal allele and is methylated on the maternal allele. Here we report an artificial system in which expression and methylation of the endogenous imprinted gene U2af1-rs1 can be affected by interaction with its own transgene in the testis. We suggest that there is a mechanism in male gametogenesis by which the U2af1-rs1 gene is kept unmethylated to be expressed in the offspring in addition to a mechanism in female gametogenesis by which the U2af1-rs1 gene is methylated and is not expressed in the offspring.

摘要

基因组印记是指基因的亲本等位基因特异性表达。这种现象背后的确切机制,可能涉及DNA甲基化,目前尚不清楚。U2af1-rs1(SP2)是一个从父本等位基因表达的印记基因,在母本等位基因上发生甲基化。在此,我们报告了一个人工系统,其中内源性印记基因U2af1-rs1的表达和甲基化可受其在睾丸中自身转基因相互作用的影响。我们认为,在雄性配子发生过程中存在一种机制,通过该机制U2af1-rs1基因保持未甲基化状态以便在后代中表达,此外在雌性配子发生过程中还存在一种机制,通过该机制U2af1-rs1基因发生甲基化且不在后代中表达。

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