A cyclophilin gene-like sequence maps to human X-chromosome

Somatic Cell and Molecular Genetics

Volumn 22, Issue 1, 1996, Pages 67-73

  Kandpal, Geeta ^a   Jacob, A N K ^a   Kandpal, Rajendra P ^a  

^a TEMPLE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPHILIN;

ARTICLE; CHROMOSOME XQ; DNA HYBRIDIZATION; GENE DELETION; GENE LOCATION; GENE LOCUS; GENE SEQUENCE; HUMAN; PRIORITY JOURNAL; SEQUENCE ANALYSIS; X CHROMOSOME; YEAST ARTIFICIAL CHROMOSOME;

AMINO ACID ISOMERASES; BASE SEQUENCE; CARRIER PROTEINS; CELL LINE; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CLONING, MOLECULAR; DNA, COMPLEMENTARY; EXONS; HUMANS; MOLECULAR SEQUENCE DATA; PEPTIDYLPROLYL ISOMERASE; SEQUENCE ANALYSIS, DNA; X CHROMOSOME;

EID: 0029893075     PISSN: 07407750     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02374377     Document Type: Article

References (23)

1. Handschumacher, R.E., Harding, M.W., Rice, J., Drugge, R.J., and Speicher, D.W. (1984). Cyclophilin: a specific cytosolic binding protein for cyclosporin A. Science 226:544-547.
2. Harding, M.W., Handschumacher, R.E., and Speicher, D.W. (1986). Isolation and amino acid sequence of cyclophilin. J. Biol. Chem. 261:8547-8555.
3. Haendler, B., Hofer-Warbinek, R., and Hofer, E. (1987). Complementary DNA for human T-cell cyclophilin. EMBO J. 6:947-950.
4. Haendler, B., and Hofer, E. (1990). Characterization of the human cyclophilin gene and of related processed pseudogenes. European J. Biochem. 190:477-482.
5. Liu, J., Albers, M.W., Chih-Ming, C., Schreiber, S.L., and Walsh, C.T. (1990). Cloning, expression, and purification of human cyclophilin in E. coli and assessment of the catalytic role of cysteines by site-directed mutagenesis. Proc. Natl. Acad. Sci. U.S.A. 87:2304-2308.
6. Price, E.R., Zydowsky, L.D., Jin, M., Baker, C.H., McKeon, F.D., and Walsh, C.T. (1991). Human cyclophilin-B: A second cyclophilin gene encodes a peptidyl-prolyl isomerase with a signal sequence. Proc. Natl. Acad. Sci. U.S.A. 88:1903-1907.
7. Danielson, P.E., Forss-Petter, S., Brow, M.A., Calavetta, L., Douglass, J., Milner, R.J. and Sutcliffe, J.G. (1988). p1B15: a cDNA clone of the rat mRNA encoding cyclophilin. DNA 7:261-267.
8. Tropschug, M., Nicholson, D.W., Hartl, F.U., Kohler, H., Pfanner, N., Wachter, E., and Neupert, W. (1988). Cyclosporin A-binding protein (cyclophilin) of Neurospora crassa. One gene codes for both the cytosolic and mitochondrial forms. J. Biol. Chem. 263:14433-14440.
9. Haendler, B., Keller, R., Hiestand, P.C., Kocher, H.P., Wegmann, G., and Movva, N.R. (1989). Yeast cyclophilin: Isolation and characterization of the protein, cDNA and gene. Gene 83:39-46.
10. Takahashi, N., Hayano, T., and Suzuki, M. (1989). Peptidyl-prolyl cis-trans isomerase is the cyclosporin A binding protein cyclophilin. Nature (London) 337:473-475.
11. Peddada, L.B., McPherson, J.D., Law, R., Wasmuth, J.J., Youderian, P., and Deans, R.J. (1992). Somatic cell mapping of the human cyclophilin B gene (PP1B) to chromosome 15. Cytogenet. Cell Genet. 60:219-221.
12. Nance, W.E., Setleff, R., McLedd, A., Sweeney, A., Cooper, C., and McConnell, F. (1971). X-linked deafness with congenital fixation of the stapedial footplate and perilymphatic gusher. Birth Defects 7:64-69.
13. DeKok, Y.J.M., van der Maarel, S.M., Bitner-Glindzicz, M., Huber, I., Monaco, A.P., Malcolm, S., Pembrey, M.E., Ropers, H.H., Cremers, F.P.M. (1995). Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4. Science 267:685-688.
14. Sambrook, J., Fritsch, E.F. and Maniatis, T. (1989). Molecular Cloning. A Laboratory Manual, 2nd Ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York.
15. Merry, D.E., Lesko, J.G., Sosnoski, D.M., Lewis, R.A., Lubinsky, M., Trask, B., van den Engh, G., Collins, F.S., and Nussbaum, R.L. (1989). Choroideremia and deafness with stapes fixation: A contiguous gene deletion syndrome in Xq21.Am. J. Hum. Genet. 45:530-540.
16. Feinberg, A.P. and Vogelstgein, B. (1983). A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem. 133:6-13.
17. Parimoo, S., Patanjali, S.R., Shukla, H., Chaplain, D., and Weissman, S.M. (1991).cDNA selection: Efficient PCR approach for the selection of cDNAs encoded in large chromosomal fragments. Proc. Natl. Acad. Sci. U.S.A. 88:9623-9627.
18. Lovett, M., Kere, J., and Hinton, L.M. (1991). Direct selection: a method for the isolation of cDNAs encoded by large genomic regions. Proc. Natl. Acad. Sci. U.S.A. 88:9628-9632.
19. Cremers, C.W.R.J. (1985). Audiologic features of the X-linked progressive mixed deafness syndrome with perilymphatic gusher during stapes surgery. Am. J. Otolaryngol. 6:243-246.
20. Phelps, P.D., Reardon, W., Pembrey, M.E., Bellman, S., Luxom, L. (1991). X-linked deafness, stapes gusher, and a distinctive defect of the inner ear. Neuroradiology 33:326-330.
21. Nussbaum, R.L., Lesko, J.G., Lewis, R.A., Ledbetter, S.A., and Ledbetter, D.H. (1987). Isolation of anonymous DNA sequences from within a submicroscopic deletion in a patient with choroideremia, deafness and mental retardation. Proc. Natl. Acad. Sci. U.S.A. 84:6521-6525.
22. Rosenberg, T., Niebuhr, E., Yang, H.M., Parvey, A., and Schwartz, M. (1987). Choroideremia, congenital deafness, and mental retardation in a family with an X-chromosome deletion. Opthalmic Pediatric Genet. 3:139-143.
23. Wells, S., Mould, S., Robins, D., Robinson, D., and Jacobs, P. (1991). Molecular and cytogenetic analysis of a familial microdeletion of Xq. J. Med. Genet. 28:163-166.