Assignment of the PSST subunit gene of human mitochondrial complex I to chromosome 19p13

被引:20
作者
Hyslop, SJ
Duncan, AMV
Pitkanen, S
Robinson, BH
机构
[1] HOSP SICK CHILDREN,RES INST,TORONTO,ON M5G 1X8,CANADA
[2] UNIV TORONTO,DEPT BIOCHEM,TORONTO,ON,CANADA
[3] UNIV TORONTO,DEPT PAEDIAT,TORONTO,ON M5S 1A1,CANADA
[4] QUEENS UNIV,DEPT PATHOL,KINGSTON,ON K7L 3N6,CANADA
[5] KINGSTON GEN HOSP,KINGSTON,ON K7L 2V7,CANADA
基金
英国医学研究理事会;
关键词
D O I
10.1006/geno.1996.0572
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
The cDNA for the PSST subunit of human mitochondrial nicotinamide adenine dinucleotide (NADH): ubiquinone oxidoreductase [complex I; NADH dehydrogenase (ubiquinone), Fe-S (20 kDa); EC 1.6.5.3] was generated by polymerase chain reaction (PCR) amplification of human cDNA. The sequence of the mature protein deduced from the cDNA codes for a protein that is closely related to the bovine protein (93% homology). Nine conservative substitutions are found in the mature protein, mainly in the N and C terminal regions, The mature human protein is missing four amino acids (PAAL) close to the N terminus that are present in the bovine protein. The N terminus of the mature protein is preceded by a presequence of 38 amino acids that, although quite different from its bovine counterpart (52% homology), has properties that are characteristic of a mitochondrial import sequence. Southern hybridization analysis predicts an estimated gene size of 3.8 kb. Northern hybridization analysis of mRNA from fibroblasts of complex I-deficient patients revealed no size or transcript level abnormalities. The cDNA of the PSST protein was used to investigate tissue-specific expression and to localize the gene for this subunit to chromosome 19p13. (C) 1996 Academic Press, Inc.
引用
收藏
页码:375 / 380
页数:6
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