CLONING OF THE CDNA FOR THE HUMAN ATP SYNTHASE OSCP SUBUNIT (ATP50) BY EXON TRAPPING AND MAPPING TO CHROMOSOME 21Q22.1-Q22.2

被引:20
作者
CHEN, HM
MORRIS, MA
ROSSIER, C
BLOUIN, JL
ANTONARAKIS, SE
机构
[1] UNIV GENEVA,SCH MED,DEPT GENET & MICROBIOL,HUMAN MOLEC GENET LAB,GENEVA,SWITZERLAND
[2] CANTONAL HOSP,DIV MED GENET,GENEVA,SWITZERLAND
关键词
D O I
10.1006/geno.1995.1176
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
Exon trapping was used to clone portions of potential genes from human chromosome 21. One trapped sequence showed striking homology with the bovine and rat ATP synthase OSCP (oligomycin sensitivity conferring protein) subunit. We subsequently cloned the full-length human ATP synthase OSCP cDNA (GDB/HGMW approved name ATP50) from infant brain and muscle libraries and determined its nucleotide and deduced amino acid sequence (EMBL/GenBank Accession No, X83218). The encoded polypeptide contains 213 amino acids, with more than 80% identity to bovine and murine ATPase OSCP subunits and over 35% identity to Saccharomyces cerevisiae and sweet potato sequences. The human ATP50 gene is located at 21q22.1-q22.2, just proximal to D21S17, in YACs 860G11 and 838C7 of the Chumakov et al. (Nature 359:380, 1992) YAC contig. The gene is expressed in all human tissues examined, most strongly in muscle and heart. This ATP50 subunit is a key structural component of the stalk of the mitochondrial respiratory chain F1F0-ATP synthase and as such may contribute in a gene dosage-dependent manner to the phenotype of Down syndrome (trisomy 21). (C) 1995 Academic Press, Inc.
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页码:470 / 476
页数:7
相关论文
共 39 条
  • [1] STRUCTURE AT 2.8-ANGSTROM RESOLUTION OF F1-ATPASE FROM BOVINE HEART-MITOCHONDRIA
    ABRAHAMS, JP
    LESLIE, AGW
    LUTTER, R
    WALKER, JE
    [J]. NATURE, 1994, 370 (6491) : 621 - 628
  • [2] BASIC LOCAL ALIGNMENT SEARCH TOOL
    ALTSCHUL, SF
    GISH, W
    MILLER, W
    MYERS, EW
    LIPMAN, DJ
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) : 403 - 410
  • [3] HUMAN CHROMOSOME-21 - GENOME MAPPING AND EXPLORATION, CIRCA 1993
    ANTONARAKIS, SE
    [J]. TRENDS IN GENETICS, 1993, 9 (04) : 142 - 148
  • [4] EXON AMPLIFICATION - A STRATEGY TO ISOLATE MAMMALIAN GENES BASED ON RNA SPLICING
    BUCKLER, AJ
    CHANG, DD
    GRAW, SL
    BROOK, JD
    HABER, DA
    SHARP, PA
    HOUSMAN, DE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) : 4005 - 4009
  • [5] CAPALDI RA, 1994, TRENDS BIOCHEM SCI, V60, P284
  • [6] Chen H. M., 1994, American Journal of Human Genetics, V55, pA255
  • [7] ISOLATION AND MAPPING OF HUMAN-CHROMOSOME-21 CDNA - PROGRESS IN CONSTRUCTING A CHROMOSOME-21 EXPRESSION MAP
    CHENG, JF
    BOYARTCHUK, V
    ZHU, YW
    [J]. GENOMICS, 1994, 23 (01) : 75 - 84
  • [8] CONTINUUM OF OVERLAPPING CLONES SPANNING THE ENTIRE HUMAN CHROMOSOME-21Q
    CHUMAKOV, I
    RIGAULT, P
    GUILLOU, S
    OUGEN, P
    BILLAUT, A
    GUASCONI, G
    GERVY, P
    LEGALL, I
    SOULARUE, P
    GRINAS, L
    BOUGUELERET, L
    BELLANNECHANTELOT, C
    LACROIX, B
    BARILLOT, E
    GESNOUIN, P
    POOK, S
    VAYSSEIX, G
    FRELAT, G
    SCHMITZ, A
    SAMBUCY, JL
    BOSCH, A
    ESTIVILL, X
    WEISSENBACH, J
    VIGNAL, A
    RIETHMAN, H
    COX, D
    PATTERSON, D
    GARDINER, K
    HATTORI, M
    SAKAKI, Y
    ICHIKAWA, H
    OHKI, M
    LEPASLIER, D
    HEILIG, R
    ANTONARAKIS, S
    COHEN, D
    [J]. NATURE, 1992, 359 (6394) : 380 - 387
  • [9] ISOLATION OF GENES FROM COMPLEX SOURCES OF MAMMALIAN GENOMIC DNA USING EXON AMPLIFICATION
    CHURCH, DM
    STOTLER, CJ
    RUTTER, JL
    MURRELL, JR
    TROFATTER, JA
    BUCKLER, AJ
    [J]. NATURE GENETICS, 1994, 6 (01) : 98 - 105
  • [10] ENZYME STRUCTURE - OUR PRIMARY SOURCE OF ATP
    CROSS, RL
    [J]. NATURE, 1994, 370 (6491) : 594 - 595