Nagao Y, Platero J S, Waheed A, Sly W S
Edward A. Doisy Department of Biochemistry and Molecular Biology, St. Louis University School of Medicine, MO 63104.
Proc Natl Acad Sci U S A. 1993 Aug 15;90(16):7623-7. doi: 10.1073/pnas.90.16.7623.
A full-length cDNA clone encoding human mitochondrial carbonic anhydrase (CA), CA V, was isolated from a human liver cDNA library. The 1123-bp cDNA includes a 55-bp 5' untranslated region, a 915-bp open reading frame, and a 153-bp 3' untranslated region. Expression of the cDNA in COS cells produced active enzyme. The 34-kDa precursor and 30-kDa mature form of CA V were identified on Western blots of COS-cell homogenates by a CA V-specific antibody raised to a synthetic peptide corresponding to the C-terminal 17 aa of CA V. Both 34-kDa and 30-kDa bands were also present in mitochondria isolated from transfected COS cells, whereas only the 30-kDa band was present in mitochondria isolated from normal human liver. The N-terminal sequence determined directly on the 30-kDa soluble CA purified from transfected COS cells indicated that processing of the precursor to mature human CA V involves removal of a 38-aa mitochondrial leader sequence. The 267-aa sequence deduced for mature human CA V shows 30-49% similarity to amino acid sequences of previously characterized human CAs (CA I-CA VII) and 76% similarity to the corresponding amino acid sequence deduced from the mouse cDNA. PCR analysis of DNAs from human-rodent somatic cell hybrids localized the gene for CA V to human chromosome 16, the same chromosome to which CA VII has previously been mapped.
从人肝脏cDNA文库中分离出一个编码人线粒体碳酸酐酶(CA)即CA V的全长cDNA克隆。这个1123bp的cDNA包含一个55bp的5'非翻译区、一个915bp的开放阅读框和一个153bp的3'非翻译区。该cDNA在COS细胞中的表达产生了活性酶。通过针对与CA V C末端17个氨基酸对应的合成肽产生的CA V特异性抗体对COS细胞匀浆进行蛋白质免疫印迹分析,鉴定出了34kDa的前体形式和30kDa成熟形式的CA V。在从转染的COS细胞中分离出的线粒体中也存在34kDa和30kDa条带,而在从正常人肝脏中分离出的线粒体中仅存在30kDa条带。直接对从转染COS细胞中纯化的30kDa可溶性CA测定的N末端序列表明前体加工成成熟人CA V涉及去除一个38个氨基酸的线粒体前导序列。推导的成熟人CA V的267个氨基酸序列与先前鉴定的人CA(CA I - CA VII)的氨基酸序列显示出30 - 49%的相似性,与从小鼠cDNA推导的相应氨基酸序列显示出76%的相似性。对人 - 啮齿动物体细胞杂种DNA进行的PCR分析将CA V基因定位到人类16号染色体,CA VII先前也被定位到该染色体上。