CpG island of rat sphingosine kinase-1 gene: tissue-dependent DNA methylation status and multiple alternative first exons

被引:96
作者
Imamura, T [1 ]
Ohgane, J [1 ]
Ito, S [1 ]
Ogawa, T [1 ]
Hattori, N [1 ]
Tanaka, S [1 ]
Shiota, K [1 ]
机构
[1] Univ Tokyo, Lab Cellular Biochem, Bunkyo Ku, Tokyo 1138657, Japan
基金
日本学术振兴会;
关键词
CpG island; DNA methylation; sphingosine kinase; brain; development; tissue specific; alternative splicing;
D O I
10.1006/geno.2001.6607
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
It is generally recognized that CpG islands are not methylated in normal tissues. SPHK1 is a key enzyme catalyzing the production of sphingosine I-phosphate, a novel signaling molecule for the proliferation and differentiation of various cells, including neural cells. Sequencing of genomic DNA and cDNA reveals that rat Sphk1a consists of six exons encoding 383 amino acids. Furthermore, we identified six alternative first exons for mRNA subtypes (Sphk1a, -b, -c, -d, -e, and -f) within a 3.7-kb CpG island. The CpG island contains a tissue-dependent, differentially methylated region (T-DMR; similar to 200 bp), which is located similar to 800 bp upstream of the first exon of Sphk1a. T-DMR is hypomethylated in the adult brain where Sphk1a is expressed, whereas it is hypermethylated in the adult heart where the gene is not expressed. In fetal tissues, hypomethylation of T-DMR is not associated with expression of Sphk1a, which suggests that differential availability of transcription factors is also likely to be involved in the mechanism of its expression. Here, we identify rat Sphk1, using multiple alternative first exons for the subtypes, and demonstrate that there is a CpG island bearing T-DMR.
引用
收藏
页码:117 / 125
页数:9
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