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人类碳酸酐酶IV基因的基因组组织及其在17号染色体q臂上的定位。

Genomic organization and localization of gene for human carbonic anhydrase IV to chromosome 17q.

作者信息

Okuyama T, Batanian J R, Sly W S

机构信息

Edward A. Doisy Department of Biochemistry and Molecular Biology, St. Louis University School of Medicine, Missouri 63104.

出版信息

Genomics. 1993 Jun;16(3):678-84. doi: 10.1006/geno.1993.1247.

Abstract

Carbonic anhydrase IV (CA IV) is a glycosylphosphatidylinositol-anchored membrane isozyme expressed on the luminal surfaces of pulmonary (and certain other) capillaries and on the luminal surface of proximal renal tubules. It is of interest for its functional importance in CO2 and HCO3- transport, its ancient evolutionary status among CA isozymes, and its possible role in inherited renal abnormalities of HCO3- transport. To determine the localization of the CA IV gene and define its genomic structure, we isolated and characterized a full-length genomic clone. The 9.5-kb gene contains eight exons and seven introns. The first exon (exon 1a) encodes the signal sequence. Exons 1b through 7 encode the remaining coding sequence. Exon 7 encodes the C terminus of the enzyme precursor, the C terminus of the mature protein and also contains the 120-bp sequence corresponding to the 3' untranslated region of the cDNA. The positions of introns 3, 4, 5, and 6 are identical with the corresponding positions of introns in the genes for the soluble CA isozymes (CA I, II, III, and VII). However, intron 1a is not found in these genes, and the positions of introns 1b and 2 in CA IV differ from the positions of the corresponding introns in genes for the soluble isozymes. The 5' upstream region of the gene (-500 to -1) is GC rich and contains 30 CpG dinucleotides. A TATA box sequence and a potential Sp1 binding site are identified upstream of the first exon. By using PCR on DNA from human/rodent somatic cell hybrids, the CA IV gene was assigned to chromosome 17.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

碳酸酐酶IV(CA IV)是一种糖基磷脂酰肌醇锚定的膜同工酶,表达于肺(及某些其他)毛细血管的管腔表面和近端肾小管的管腔表面。它因其在二氧化碳和碳酸氢根转运中的功能重要性、在碳酸酐酶同工酶中的古老进化地位以及在遗传性碳酸氢根转运肾脏异常中的可能作用而备受关注。为了确定CA IV基因的定位并定义其基因组结构,我们分离并鉴定了一个全长基因组克隆。该9.5 kb的基因包含8个外显子和7个内含子。第一个外显子(外显子1a)编码信号序列。外显子1b至7编码其余的编码序列。外显子7编码酶前体的C末端、成熟蛋白的C末端,还包含与cDNA的3'非翻译区相对应的120 bp序列。内含子3、4、5和6的位置与可溶性碳酸酐酶同工酶(CA I、II、III和VII)基因中内含子的相应位置相同。然而,在这些基因中未发现内含子1a,并且CA IV中内含子1b和2的位置与可溶性同工酶基因中相应内含子的位置不同。该基因的5'上游区域(-500至-1)富含GC,包含30个CpG二核苷酸。在第一个外显子上游鉴定出一个TATA盒序列和一个潜在的Sp1结合位点。通过对人/啮齿动物体细胞杂种的DNA进行PCR,将CA IV基因定位于17号染色体。(摘要截短于250字)

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