MSG1 (melanocyte-specific gene 1):: mapping to chromosome Xq13.1, genomic organization, and promoter analysis

被引:25
作者
Fenner, MH
Parrish, JE
Boyd, Y
Reed, V
MacDonald, M
Nelson, DL
Isselbacher, KJ
Shioda, T
机构
[1] Massachusetts Gen Hosp, Ctr Canc, Lab Tumor Biol, Charlestown, MA 02129 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] MRC, Mammalian Genet Unit, Didcot OX11 0RD, Oxon, England
[4] Massachusetts Gen Hosp, Mol Neurogenet Unit, Charlestown, MA 02129 USA
关键词
D O I
10.1006/geno.1998.5383
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
MSG1 (melanocyte-specific gene 1) is a recently isolated gene predominantly expressed in cultured normal melanocytes and pigmented melanoma cells, MSG1 encodes a 27-kDa nuclear protein that has strong intrinsic transcriptional transactivating activity. In this report, the human MSG1 gene was mapped to chromosome Xq13.1 using X chromosome-specific somatic cell hybrids, and the mouse Msg1 gene was mapped 1.9 +/- 1.3 cM proximal to Xist using an interspecific backcross panel. Both the human and the mouse MSG1 genes consist of three exons and two introns within 5 kb of genomic DNA, and their genomic structures are highly conserved. Southern blot analysis suggests the existence of MSG1 homologues in chicken, zebrafish, and Drosophila. A 2.0-kb fragment of the 5'-flanking region of the mouse Msg1 gene contains a TATA box and potential binding sites for several transcription factors including USF, Brn-3, Brn-2, TFE3, Oct-1, AP-2, and Spl. This promoter fragment activates transcription of a reporter gene in pigmented melanoma cells, but not in amelanotic melanoma cells or nonmelanocytic cells, indicating that Msg1 expression is at least partially regulated at the transcriptional level, (C) 1998 Academic Press
引用
收藏
页码:401 / 407
页数:7
相关论文
共 32 条
[1]   GENETICS, DEVELOPMENT, AND MALIGNANCY OF MELANOCYTES [J].
BENNETT, DC .
INTERNATIONAL REVIEW OF CYTOLOGY - A SURVEY OF CELL BIOLOGY, VOL 146, 1993, 146 :191-260
[2]   An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome [J].
Blair, HJ ;
Uwechue, IC ;
Barsh, GS ;
Rowe, PSN ;
Boyd, Y .
GENOMICS, 1998, 48 (01) :128-131
[3]  
BOYD Y, 1997, MAMM GENOME, V7, P313
[4]   LOCALIZATION OF THE X-INACTIVATION CENTER ON THE HUMAN X-CHROMOSOME IN XQ13 [J].
BROWN, CJ ;
LAFRENIERE, RG ;
POWERS, VE ;
SEBASTIO, G ;
BALLABIO, A ;
PETTIGREW, AL ;
LEDBETTER, DH ;
LEVY, E ;
CRAIG, IW ;
WILLARD, HF .
NATURE, 1991, 349 (6304) :82-84
[5]   The mottled mouse as a model for human Menkes disease: Identification of mutations in the Atp7a gene [J].
Cecchi, C ;
Biasotto, M ;
Tosi, M ;
Avner, P .
HUMAN MOLECULAR GENETICS, 1997, 6 (03) :425-433
[6]   Human/mouse homology relationships [J].
DeBry, RW ;
Seldin, MF .
GENOMICS, 1996, 33 (03) :337-351
[7]   The zebrafish: Heritable disorders in transparent embryos [J].
Driever, W ;
Fishman, MC .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (08) :1788-1794
[8]   Msg1 and Mrg1, founding members of a gene family, show distinct patterns of gene expression during mouse embryogenesis [J].
Dunwoodie, SL ;
Rodriguez, TA ;
Beddington, RSP .
MECHANISMS OF DEVELOPMENT, 1998, 72 (1-2) :27-40
[9]  
GANSS R, 1994, J BIOL CHEM, V269, P29808
[10]   Genetics of cutaneous melanoma and nevi [J].
Greene, MH .
MAYO CLINIC PROCEEDINGS, 1997, 72 (05) :467-474