Zhang L P, Stroud J C, Walter C A, Adrian G S, McCarrey J R
Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, Texas 78245, USA.
Biol Reprod. 1998 Aug;59(2):284-92. doi: 10.1095/biolreprod59.2.284.
Transcription of the autosomal phosphoglycerate kinase gene, Pgk-2, is initiated at the onset of meiosis during spermatogenesis in mammals. However, in the mouse, the 5' portion of the endogenous Pgk-2 coding sequence undergoes a specific demethylation event that precedes transcriptional activation by 10-12 days. Here we show that transgenes consisting of the Pgk-2 core promoter ligated to the CAT reporter gene undergo a similar tissue-, stage-, and cell type-specific demethylation in the 5' portion of the CAT coding sequence, whereas transgenes consisting of the CAT reporter sequence alone, or of the CAT sequence ligated to the CpG island-containing transferrin gene promoter, demonstrate different patterns of demethylation. These results indicate that specific promoter sequences can influence the pattern of tissue-specific demethylation within different genes and that a signal for spermatogenic cell-specific demethylation resides within the core promoter of the mammalian Pgk-2 gene.
常染色体磷酸甘油酸激酶基因Pgk - 2的转录在哺乳动物精子发生过程中减数分裂开始时启动。然而,在小鼠中,内源性Pgk - 2编码序列的5'部分会发生特定的去甲基化事件,该事件比转录激活提前10 - 12天。我们在此表明,由Pgk - 2核心启动子与CAT报告基因连接而成的转基因在CAT编码序列的5'部分经历了类似的组织、阶段和细胞类型特异性去甲基化,而仅由CAT报告序列组成的转基因,或由CAT序列与含CpG岛的转铁蛋白基因启动子连接而成的转基因,则表现出不同的去甲基化模式。这些结果表明,特定的启动子序列可以影响不同基因内组织特异性去甲基化的模式,并且精子发生细胞特异性去甲基化的信号存在于哺乳动物Pgk - 2基因的核心启动子内。