Transcriptional mapping in a 700-kb region around the DXS52 locus in Xq28: Isolation of six novel transcripts and a novel ATPase isoform (hPMCA5)

Genome Research

Volumn 6, Issue 6, 1996, Pages 478-491

  Heiss, Nina S ^a   Rogner, Ute C ^a   Kioschis, Petra ^a   Korn, Bernhard ^a   Poustka, Annemarie ^a  

^a GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE (CALCIUM); BIGLYCAN; CENTRIN; COMPLEMENTARY DNA; ISOENZYME; MELANOMA ANTIGEN; MESSENGER RNA; MELANOMA SPECIFIC ANTIGENS; MELANOMA-SPECIFIC ANTIGENS; PRIMER DNA; PROTEOGLYCAN; SCLEROPROTEIN; TUMOR PROTEIN;

ARTICLE; CHROMOSOME XQ; DNA TRANSCRIPTION; EXON; GENE ISOLATION; GENE MAPPING; HUMAN; HUMAN TISSUE; MARKER GENE; NORTHERN BLOTTING; PRIORITY JOURNAL; SEQUENCE TAGGED SITE; AMINO ACID SEQUENCE; CHROMOSOME MAP; GENE EXPRESSION; GENETIC DISORDER; GENETIC MARKER; GENETIC TRANSCRIPTION; GENETICS; MOLECULAR CLONING; MOLECULAR GENETICS; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; X CHROMOSOME; YEAST ARTIFICIAL CHROMOSOME;

AMINO ACID SEQUENCE; BLOTTING, NORTHERN; CALCIUM-TRANSPORTING ATPASES; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CLONING, MOLECULAR; DNA PRIMERS; DNA, COMPLEMENTARY; EXONS; EXTRACELLULAR MATRIX PROTEINS; GENE EXPRESSION; GENETIC DISEASES, INBORN; GENETIC MARKERS; HUMANS; MOLECULAR SEQUENCE DATA; NEOPLASM PROTEINS; PROTEOGLYCANS; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY, AMINO ACID; TRANSCRIPTION, GENETIC; X CHROMOSOME;

EID: 0029662195     PISSN: 10549803     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (14)

1. Addison, M. and M.S. Rice. 1965. The association of dyskeratosis congenita and Fanconi's anaemia. Med. J. Aust. 1: 797-799.
2. Adès, L.C., A.K. Oedeon, M.J. Wilson, M. Latham, M.W. Partington, J.C. Mulley, J. Nelson, K. Lui, and D.O. Silence. 1993. Barth Syndrome: Clinical features and confirmation of gene localisation to distal Xq28. Am J. Med. Genet. 45: 327-334.
3. Altschul, S.F., W. Gish, W. Miller, E.W. Meyers, and D.J. Lipman. 1990. Basic alignment search tool. J. Mol. Biol. 215: 403-410.
4. Bell, M.V., M.N. Patterson, H.R. Dorkins, and K.E. Davies. 1989. Physical mapping of DXS134 close to the DXS52 locus. Hum. Genet. 82: 27-30.
5. Bernardi, G. 1989. The isochore organization of the human genome. Annu. Rev. Genet. 23: 637-661.
6. Biancalana, V., B. Le Marec, S. Odent, J.A.M.J. van den Hurk, and A. Hanauer. 1991. Oto-palato-digital syndrome type I: Further evidence for assignment of the locus to Xq28. Hum. Genet. 88: 228-230.
7. Bione, S., F. Tamanini, E. Maestrini, C. Tribioli, A. Poustka, G. Torri, S. Rivella, and D. Toniolo. 1993. Transcriptional organisation of a 450-kb region of the human X chromosome in Xq28. Proc. Natl. Acad. Sci. 90: 10977-10981.
8. Brennan, M.B. and U. Hochgeschwender. 1995. Commentary: So many needles, and so much hay. Hum. Mol. Genet. 4: 153-156.
9. Brown, W.T., A. Gross, C. Chan, E.G. Jenkins, J.-L. Mandel, I. Oberlé, B. Arveiler, G. Novelli, S. Thiobodeau, R. Hagerman, K. Summers, G. Turner, B.N. White, L. Mulligan, C. Forster-Gibson, J.J.A. Holden, B. Zoll, M. Krawczak, P. Goonewardena, K.H. Gustavson, U. Pettersson, G. Holmgren, C. Schwartz, P.M. Howard-Peebles, P. Murphy, W.R. Breg, H. Veenema, and N.J. Carpenter. 1988. Multilocus analysis of the fragile X syndrome. Hum. Genet. 78: 201-205.
10. Buckler, A., D. Chang, S. Graw, D. Brook, D. Haber, P. Sharp, and D. Housman. 1991. Exon amplification: A strategy to isolate mammalian genes based on RNA splicing. Proc. Natl. Acad. Sci. 88: 4005-4009.
11. Traversari, C., P. van den Bruggen, I.F. Luescher, C. Lurquin, P. Chomez, A. van Pel, E. De Plaen, A. Amar-Costesec, and T. Boon. 1992. A nonapeptide encoded by human gene MAGE-1 is recognized on HLA-A1 by cytolytic T lymphocytes directed against tumor antigen MZ2-E. J. Exp. Med. 176: 1453-1457.
12. van den Bruggen, P., C. Traversari, P. Chomez, E. Lurquin, B. De Plaen, A. van den Eynde, A. Knuth, and T. Boon. 1991. A gene eoncoding an antigen recognized by cytolytic T lymphocytes on a human melanoma. Science 254: 1643-1647.
13. 2+ ATPases isoforms 2 (ATPB2) and 3 (ATPB3) to human chromosomes 3p26-p25 and Xq28, respectively. Cytogenet. Cell Genet. 67: 41-45.
14. Zuffardi, O. and M. Fraccaro. 1982. Gene mapping and serendipity. The locus for Torticollis, Keloids, Crytorchidism and Renal Dysplasia (31430, McKusick) is at Xq28, distal to the G6PD locus. Hum. Genet. 62: 280-281.