Cloning of the human NADH: Ubiquinone oxidoreductase subunit B13: Localization to Chromosome 7q32 and identification of a pseudogene on 11p15

Mammalian Genome

Volumn 8, Issue 1, 1997, Pages 60-61

  Russell, M W ^a,b   Du Manoir, S ^b   Collins, F S ^b   Brody, L C ^b  

^a UNIVERSITY OF MICHIGAN   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; OXIDOREDUCTASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

AMINO ACID SEQUENCE; ARTICLE; CHROMOSOME 11; CHROMOSOME 7; CHROMOSOME MAP; GENETICS; HUMAN; MOLECULAR CLONING; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PSEUDOGENE; SEQUENCE HOMOLOGY; SEQUENCE TAGGED SITE;

AMINO ACID SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 7; CLONING, MOLECULAR; CONSERVED SEQUENCE; DNA, COMPLEMENTARY; ELECTRON TRANSPORT COMPLEX I; HUMANS; MOLECULAR SEQUENCE DATA; NADH, NADPH OXIDOREDUCTASES; PSEUDOGENES; SEQUENCE HOMOLOGY, AMINO ACID; SEQUENCE TAGGED SITES;

EID: 0030631582     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900350     Document Type: Article

References (14)

1. Adams, M.D., Soares, M.B., Kerlavage, A.R., Fields, C., Venter, J.C. (1993). Rapid cDNA sequencing (expressed sequence tags) from a directionally cloned human infant brain cDNA library. Nature Genet., 4, 373-80.
2. Altschul, S.F., Gish, W., Miller, W., Myers, E.W., Lipman, D.J. (1990). Basic local alignment search tool. J. Mol. Biol. 215, 403-10.
3. Gu, J.Z., Lin, X., Wells, D.E. (1996). The human B22 subunit of the NADH-ubiquinone oxidoreductase maps to the region of chromosome 8 involved in branchio-oto-renal syndrome. Genomics 35, 6-10.
4. Kozak, M. (1987). An analysis of 5′-noncoding sequences from 699 vertebrate messenger RNAs. Nucleic Acids Res. 15, 8125-8148.
5. Moreadith, R.W., Cleeter, M.W.J., Ragan, I.C., Batshaw, M.L., Lehninger, A.L. (1987). Congenital deficiency of two polypeptide subunits of the iron-protein fragment of mitochondrial complex I. J. Clin. Invest. 79, 463-467.
6. Morgan-Hughes, J.A., Schapira, A.H.V., Cooper, J.M., Clark, J.B. (1988). Molecular defects of NADH-ubiquinone oxidoreductase (Complex I) in mitochodrial diseases. J. Bioenerg. Biomembr. 20, 365-382.
7. Neupert, W., Hartl, F.U., Craig, E.A., Pfanner, N. (1990). How do polypeptides cross the mitochondrial membranes? Cell 63, 447-50.
8. Parker, W.D. Jr., Boyson, S.J., Parks, J.K. (1989). Abnormalities of the electron transport chain in idiopathic Parkinson's disease. Ann. Neurol. 26, 719-723.
9. Pata, I., Metspalu, A. (1993). A dinucleotide repeat polymorphism at the ribosomal protein S6 (RP6) gene. Hum. Mol. Genet. 2, 1749.
10. Schapira, A.H.V., Cooper, J.M., Morgan-Hughes, J.A., Patel, S.D., Cleeter, M.J.W., Ragan, C.I., Clark, J.B. (1988). Molecular basis of mitochondrial myopathies: polypeptide analysis in complex-I deficiency. Lancet 8584, 500-503.
11. Schröck, E., Badger, P., Larson, D., Erdos, M., Wynshaw-Boris, A., Ried, T., Brody, L. (1996). The murine homolog of the human breast and ovarian cancer susceptibility gene Brca1 maps to mouse chromosome 11D. Hum. Genet. 97, 256-259.
12. Shepard, N.S., Pfrogner, B.D., Coulby, J.N., Ackerman, S.L., Vaidyanathan, G., Sauer, R.H., Balkenhol, T.C., Sternberg, N. (1994). Preparation and screening of an arrayed human genomic library generated with the P1 cloning system. Proc. Natl. Acad. Sci. USA 91, 2629-2633.
13. Shoffner, J.M., Wallace, D.C. (1995). Oxidative phosphorylation diseases. In The Metabolic and Molecular Bases of Inherited Disease, C.R. Scriver, A.L. Beaudet, W.S. Sly, D. Valle, eds. (New York: McGraw-Hill, Inc.) pp. 1535-1609.
14. Walker, J.E., Arizmendi, J.M., Dupuis, A., Fearnley, I.M., Finel, M., Medd S.M., Pilkington, S.J., Runswick, M.J., Skehel, J.M. (1992). Sequences of 20 subunits of NADH:uniquinone oxidoreductase from bovine heart mitochodria. J. Mol. Biol. 226, 1051-1072.