Direct evidence for two distinct forms of the flavoprotein subunit of human mitochondrial complex II (succinate-ubiquinone reductase)

被引:25
作者
Tomitsuka, E
Hirawake, H
Goto, Y
Taniwaki, M
Harada, S
Kita, K
机构
[1] Univ Tokyo, Grad Sch Med, Dept Biomed Chem, Bunkyo Ku, Tokyo 1130033, Japan
[2] Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Dept Mental Retardat & Birth Defect Res, Tokyo 1878502, Japan
[3] Kyoto Prefectural Univ Med, Dept Clin Mol Genet & Lab Med, Kamigyo Ku, Kyoto 6020841, Japan
[4] Univ Tokyo, Grad Sch Pharmaceut Sci, Dept Biol Struct, Bunkyo Ku, Tokyo 1130033, Japan
关键词
complex II; flavoprotein subunit; human mitochondria; isoforms; succinate-ubiquinone reductase;
D O I
10.1093/jb/mvg144
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
Succinate-ubiquinone reductase (complex II) is an important enzyme complex in both the tricarboxylic acid cycle and aerobic respiration. A recent study showed that defects in human complex II are associated with cancers as well as mitochondrial diseases. Mutations in the four subunits of human complex II are associated with a wide spectrum of clinical presentations. Such tissue-specific clinical symptoms suggest the presence of multiple isoforms of the subunits, but subunit isoforms have not been previously reported. In the present study, we identified two distinct cDNAs for the human flavoprotein subunit (Fp) from a single individual, and demonstrated expression of these two isoforms in skeletal muscle, liver, brain, heart and kidney. Interestingly, one of the Fp isoforms was encoded as an intronless gene.
引用
收藏
页码:191 / 195
页数:5
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