Cloning, expression, and chromosomal assignment of the human mitochondrial intermediate peptidase gene (MIPEP)

Genomics

Volumn 40, Issue 3, 1997, Pages 493-496

  Chew, Anne ^a   Buck, Elizabeth A ^a   Peretz, Shani ^a   Sirugo, Giorgio ^a   Rinaldo, Piero ^a   Isaya, Grazia ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PEPTIDASE;

ARTICLE; CHROMOSOME MAP; DNA PROBE; ENZYME ACTIVITY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE ASSIGNMENT; GENE EXPRESSION; MOLECULAR CLONING; NORTHERN BLOTTING; OXIDATIVE PHOSPHORYLATION; PATHOPHYSIOLOGY; PRIORITY JOURNAL; SCREENING; SEQUENCE HOMOLOGY;

EID: 0031569417     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.4586     Document Type: Article

References (20)

1. 1. Attardi, G., and Schatz, G. (1988). Biogenesis of mitochondria. Annu. Rev. Cell. Biol. 4: 289-333.
2. 2. Bourgeron, T., Rustin, P., Chretien, D., Birch-Machin, M., Bourgeois, M., Viegas-Pequignot, E., Munnich, A., and Rotig, A. (1995). Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. Nature Genet. 11: 144149.
3. 3. Branda, S. S., and Isaya, G. (1995). Prediction and identification of new natural substrates of the yeast mitochondrial intermediate peptidase. J. Biol. Chem. 270: 27366-27373.
4. 4. Chew, A., Rollins, R. A., Sakati, W. A., and Isaya, G. (1996). Mutations in a putative zinc-binding site inactivate the mitochondrial intermediate peptidase. Biochem. Biophys. Res. Commun. 226: 822-829.
5. 5. Dougherty, K. M., Swanson, D. A., Brody, L. C., and Valle, D. (1993). Expression and processing of human ornithine-aminotransferase in Saccharomyces cerevisiae. Hum. Mol. Genet. 2: 1835-1840.
6. 6. Guilford, P., Ben Arab, S., Blanchard, S., Levilliers, J., Weissenbach, J., Drira, M., and Petit, C. (1994). A non-syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q. Nature Genet. 6: 24-28.
7. 7. Hendrick, J. P., Hodges, P. E., and Rosenberg, L. E. (1989). Survey of amino-terminal proteolytic cleavage sites in mitochondrial precursor proteins: Leader peptides cleaved by two matrix proteases share a three amino acid motif. Proc. Natl. Acad. Sci. USA 86: 4056-4060.
8. 8. Heng, H. H. Q., Squire, J., and Tsui, L.-C. (1992). High resolution mapping of mammalian genes by in situ hybridization to free chromatin. Proc. Natl. Acad. Sci. USA 89: 9509-9513.
9. 9. Hwang, D. M., Fung, Y. W., Wang, R. X., Laurenssen, C. M., Ng, S. H., Lam, M. Y., Tsui, K. W., Fung, K. P., Waye, M., Lee, C. Y., and Liew, C. C. (1995). Analysis of expressed sequence tags from a fetal human heart cDNA library. Genomics 30: 293-298.
10. 10. Isaya, G., and Kalousek, F. (1995). Mitochondrial intermediate peptidase. Methods Enzymol. 248: 556-567.
11. 11. Isaya, G., Miklos, D., and Rollins, R. A. (1994). MIP1, a new yeast gene homologous to rat mitochondrial intermediate peptidase, is required for oxidative metabolism in Saccharomyces cerevisiae. Mol. Cell. Biol. 14: 5603-5616.
12. 12. Isaya, G., Sakati, W. R., Rollins, R. A., Shen, G. P., Hanson, L. E., Ullrich, R. C., and Novotny, C. P. (1995). Mammalian mitochondrial intermediate peptidase: Structure/function analysis of a new homologue from Schizophyllum commune and relationship to Thimet oligopeptidases. Genomics 28: 450-461.
13. 13. Johns, D. R. (1995). Mitochondrial DNA and disease. N. Engl. J. Med. 333: 638-644.
14. 14. Ma, L., and Spremulli, L. L. (1995). Cloning and sequence analysis of the human mitochondrial translational initiation factor 2 cDNA. J. Biol. Chem. 270: 1859-1865.
15. 15. Noguchi, S., McNally, E. M., Ben Othmane, K., Hagiwara, Y., Mizuno, Y., Yoshida, M., Yamamoto, H., Bonnemann, C. G., Gussoni, E., Denton, P. H., Kyriakides, T., Middleton, L., Hentati, F., Ben Hamada, M., Nonaka, I., Vance, J. M., Kunkel, L. M., and Ozawa, E. (1995). Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy. Science 270: 819-821.
16. 16. Schon, E. A., Hirano, M., and DiMauro, S. (1994). Mitochondrial encephalomyopathies: Clinical and molecular analysis. J. Bioeng. Biomembr. 26: 291-299.
17. 17. Schutte, M., daCosta, L. T., Hahn, S. A., Moskaluk, C., Hoque, A. T. M., Rozenblum, E., Weinstein, C. L., Bittner, M., Meltzer, P. S., Trent, J. M., Yeo, C. J., Hruban, R. H., and Kern, S. E. (1995). Identification by representational difference analysis of a homozygous deletion in pancreatic carcinoma that lies with the BRC2 region. Proc. Natl. Acad. Sci. USA 92: 5950-5954.
18. 18. Shoffner, J. M., and Wallace, D. C. Oxidative phosphorylation diseases. (1995). In "The Metabolic and Molecular Basis of Inherited Disease" (C. R. Scriver, A. L. Beaudet, W. S. Sly, and D. Valle, Eds.), 7th ed., pp. 1535-1548, McGraw-Hill, New York.
19. 19. Suomalainen, A., Kaukonen, J., Amati, P., Timonen, R., Haltia, M., Weissenbach, J., Zeviani, M., Somer, H., and Peltonen, L. (1995). An autosomal locus predisposing to deletions of mitochondrial DNA. Nature Genet. 9: 146-151.
20. 20. Tiranti, V., Rossi, E., Ruiz-Carrillo, A., Rossi, G., Rocchi, M., DiDonato, S., Zuffardi, O., and Zeviani, M. (1995). Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis. Genomics 25: 559-564.