Gene structure and chromosomal localization of mouse S-adenosylmethionine decarboxylase

被引:8
|
作者
Nishimura, K
Kashiwagi, K
Matsuda, Y
Jänne, OA
Igarashi, K
机构
[1] Chiba Univ, Fac Pharmaceut Sci, Inage Ku, Chiba 2638522, Japan
[2] Hokkaido Univ, Grad Sch Environm Earth Sci, Div Biosci, Lab Cytogenet, Sapporo, Hokkaido 0600810, Japan
[3] Hokkaido Univ, Fac Sci, Chromosome Res Unit, Sapporo, Hokkaido 0600810, Japan
[4] Univ Helsinki, Dept Clin Chem, FIN-00014 Helsinki, Finland
[5] Univ Helsinki, Dept Physiol, Inst Biomed, FIN-00014 Helsinki, Finland
关键词
gene organization; polyamines; S-adenosylmethionine decarboxylase; upstream open reading frame;
D O I
10.1016/S0378-1119(99)00355-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The structure of the mouse S-adenosylmethionine decarboxylase (AdoMetDC) gene has been determined. The mouse gene (AMD1) consisted of eight exons and seven introns, similar to the rat AdoMetDC gene, and was mapped to chromosome 10. The characteristics of AMD1 gene were as follows: (1) The region of the promoter necessary for maximal transcriptional activity was located about 400 nucleotides upstream of the transcriptional initiation point, and contained a TATA box and two GC boxes. The transcriptional activity of the promoter was nearly equal to that of the SV40 promoter. (2) Two polyadenylation signals for transcription were observed, and the larger AdoMetDC mRNA, which is the dominant form of mRNA, corresponded to mRNA that is generated using the second polyadenylation signal. (3) Using stable transfectants, we confirmed that the upstream open reading frame (uORF) in the 5'-untranslated region (5'-UTR) of AdoMetDC mRNA functioned as a negative regulatory element. Lower concentrations of polyamines affect both stimulation and inhibition of AdoMetDC synthesis, through the uORF in the mRNA, than affect general protein synthesis. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:343 / 350
页数:8
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