Cited by 22ATP Synthase and ATPases ResearchMitochondrial Function and PathologyDown syndrome and intellectual disability research

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Cloning of the cDNA for the Human ATP Synthase OSCP Subunit (ATP50) by Exon Trapping and Mapping to Chromosome 21q22.1-q22.2

Abstract

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 ATP5O 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 ATP5O 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).

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Crossref · 10.1006/geno.1995.1176

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Metadata

Authors
Chen, H., Morris, M. A., Rossier, C., Blouin, J.-L., & Antonarakis, S. E.
Affiliations
University of Geneva (CH)
Venue
Genomics
Publisher
Elsevier BV
Published
1995-08
Volume
28
Issue
3
Pages
470-476
ISSN
0888-7543 (ISSN-L)
OpenAlex
W1984793777
Cited by
22
References
0
Citations by year
2025: 1 · 2024: 1 · 2020: 2 · 2019: 1 · 2012: 1
FWCI
1.11
Type
journal article
Language
en
Open access
closed
Locations
  • Genomics (publishedVersion)
  • PubMed (publishedVersion)
  • Archive ouverte UNIGE (University of Geneva) (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › ATP Synthase and ATPases Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Down syndrome and intellectual disability research
Keywords
OSCP, cDNA cloning, exon trapping, mitochondrial respiratory chain, gene dosage, Down syndrome, tissue-specific gene expression, sequence homology
MeSH terms
Adenosine Triphosphatases, Amino Acid Sequence, Animals, Base Sequence, Carrier Proteins, Cattle, Chromosome Mapping, Chromosomes, Human, Pair 21, Cloning, Molecular, Exons, Proton-Translocating ATPases, Humans, Infant, Membrane Proteins, Molecular Sequence Data, Blotting, Southern, Blotting, Northern, Sequence Homology, Amino Acid, DNA, Complementary, Mitochondrial Proton-Translocating ATPases, Rats

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