Isolation and sequence of the human cytochrome c oxidase subunit VIIaL gene

被引:12
作者
Hüttemann, M
Mühlenbein, N
Schmidt, TR
Grossman, LI
Kadenbach, B [1 ]
机构
[1] Univ Marburg, Fachbereich Chem, D-35032 Marburg, Germany
[2] Wayne State Univ, Sch Med, Ctr Mol Med & Genet, Detroit, MI 48201 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2000年 / 1492卷 / 01期
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
cytochrome c oxidase; human COX subunit IV; human COX subunit VIIaL; human COX subunit VIIaL gene structure;
D O I
10.1016/S0167-4781(00)00087-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gene for human cytochrome c oxidase subunit VIIa liver isoform (COX7AL) was isolated and its sequence determined and analyzed. The three introns of the gene are considerably larger than those of the heart isoform of subunit VIIa (COX7AH), but the position of the introns relative to the cDNA sequences is homologous between the two genes. Comparison with other isolated COX7AL genes suggests that the promoter region binding motifs for transcription factors have evolved along with the coding region. In fibroblasts cultured originally from a Leigh's disease patient, a shortened COX7AL cDNA was identified by RT-PCR, consisting of exon I joined to exon IV, omitting exons II and III. No mutation could be identified in COX7AL of the patient, suggesting that the shortened cDNA is due to an alteration of the genome during cell culture. A surprising transcription of COX7AH was observed in cultured fibroblasts, suggesting a potential utility of these cells for study of its gene expression. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:252 / 258
页数:7
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