Genomic structure of a novel LIM domain gene (ZNF185) in Xq28 and comparisons with the orthologous murine transcript

被引:31
作者
Heiss, NS
Gloeckner, G
Bachner, D
Kioschis, P
Klauck, SM
Hinzmann, B
Rosenthal, A
Herman, GE
Poustka, A
机构
[1] DEUTSCH KREBSFORSCHUNGSZENTRUM,DEPT MOL GENOME ANAL,D-69120 HEIDELBERG,GERMANY
[2] INST MOL BIOTECHNOL,DEPT MOL GENOME ANAL,D-07745 JENA,GERMANY
[3] GESELL BIOTECHNOL FORSCH MBH,DEPT GENE REGULAT & DIFFERENTIAT,D-38124 BRAUNSCHWEIG,GERMANY
[4] BAYLOR COLL MED,DEPT MOL & HUMAN GENET & PEDIAT,HOUSTON,TX 77030
[5] CHILDRENS HOSP RES FDN,DEPT PEDIAT,COLUMBUS,OH 43210
关键词
D O I
10.1006/geno.1997.4810
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Construction of a transcript map in the DXS52 region in Xq28 had previously led to the isolation of a cDNA with a LIM zinc finger domain in the carboxyl terminus. In parallel, the orthologous murine transcript was isolated from the syntenic region. The human and mouse cDNAs have been designated ZNF185 and Zfp185, respectively. By integrating the cDNA sequence with the cosmid derived genomic sequence the exon-intron structure of the 3' end of the ZNF185 gene was resolved. Comparative sequence analyses of the human genomic sequence with the full-length murine cDNA facilitated prediction of the 5' end of the gene. The selective expression of three transcripts corresponding to the ZNF185 gene and a related gene was shown by Northern and Southern blots. In situ hybridizations revealed a nonubiquitous and stage-specific expression of Zfp185, especially in differentiating connective tissue. Since LIM proteins regulate cellular proliferation and/or differentiation by diverse mechanisms, and some have directly been associated with disease, conceivably ZNF185 may represent a candidate for a disease-causing gene linked to Xq28. Knowledge of the genomic structure will permit detailed mutation analyses. (C) 1997 Academic Press.
引用
收藏
页码:329 / 338
页数:10
相关论文
共 52 条
[31]   THE PROLINE-RICH TRANSCRIPTIONAL ACTIVATOR OF CTF/NF-I IS DISTINCT FROM THE REPLICATION AND DNA-BINDING DOMAIN [J].
MERMOD, N ;
ONEILL, EA ;
KELLY, TJ ;
TJIAN, R .
CELL, 1989, 58 (04) :741-753
[32]  
MIZUNO K, 1994, ONCOGENE, V9, P1605
[33]   LINKAGE TO XQ28 IN A FAMILY WITH NONSPECIFIC X-LINKED MENTAL-RETARDATION [J].
NORDSTROM, AM ;
PENTTINEN, M ;
VONKOSKULL, H .
HUMAN GENETICS, 1992, 90 (03) :263-266
[34]   THE TELOMERIC REGION OF THE HUMAN X-CHROMOSOME LONG ARM - PRESENCE OF A HIGHLY POLYMORPHIC DNA MARKER AND ANALYSIS OF RECOMBINATION FREQUENCY [J].
OBERLE, I ;
DRAYNA, D ;
CAMERINO, G ;
WHITE, R ;
MANDEL, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (09) :2824-2828
[35]  
PEREZALVARADO GC, 1994, STRUCT BIOL, V1, P388
[36]  
PETIT NMR, 1996, GENOMICS, V36, P118
[37]   HOW EUKARYOTIC TRANSCRIPTIONAL ACTIVATORS WORK [J].
PTASHNE, M .
NATURE, 1988, 335 (6192) :683-689
[38]   A DYE-BUOYANT-DENSITY METHOD FOR DETECTION AND ISOLATION OF CLOSED CIRCULAR DUPLEX DNA - CLOSED CIRCULAR DNA IN HELA CELLS [J].
RADLOFF, R ;
BAUER, W ;
VINOGRAD, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1967, 57 (05) :1514-&
[39]   A COMPARATIVE TRANSCRIPTIONAL MAP OF A REGION OF 250 KB ON THE HUMAN AND MOUSE X-CHROMOSOME BETWEEN THE G6PD AND THE FLN1 GENES [J].
RIVELLA, S ;
TAMANINI, F ;
BIONE, S ;
MANCINI, M ;
HERMAN, G ;
CHATTERJEE, A ;
MAESTRINI, E ;
TONIOLO, D .
GENOMICS, 1995, 28 (03) :377-382
[40]   Transcriptional analysis of the candidate region for incontinentia pigmenti (IP2) in Xq28 [J].
Rogner, UC ;
Heiss, NS ;
Kioschis, P ;
Wiemann, S ;
Korn, B ;
Poustka, A .
GENOME RESEARCH, 1996, 6 (10) :922-934