Two members of the human MAGEB gene family located in Xp21.3 are expressed in tumors of various histological origins

被引:124
作者
Lurquin, C
De Smet, C
Brasseur, F
Muscatelli, F
Martelange, V
De Plaen, E
Brasseur, R
Monaco, AP
Boon, T
机构
[1] Univ Catholique Louvain 7459, Ludwig Inst Canc Res, Brussels Branch, B-1200 Brussels, Belgium
[2] Catholic Univ Louvain, Cellular Genet Unit, B-1200 Brussels, Belgium
[3] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[4] Fca Sci Agron Gembloux, Ctr Biophys Mol Numer, B-5030 Gembloux, Belgium
基金
英国惠康基金;
关键词
D O I
10.1006/geno.1997.5052
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
Genes of the MAGE family direct the expression of tumor antigens recognized on a human melanoma by autologous cytolytic T lymphocytes. Twelve closely related MAGE genes are located in the Xq28 region. These genes share 60-98% nucleotide identity in their coding region. The presence of homologous genes in a region of Xp21.3 has been reported previously. We obtained the complete sequence of a 42-kb stretch of this region. It contains four MAGE-related genes, which we propose to name MAGE-B1, B2, B3, and B4 (HGMW-approved symbols MAGEB1, MAGEB2, MAGEB3, and MAGEB4). The coding regions of these genes share 66-81% nucleotide identity and show 45-63% identity with those of the MAGE genes located in Xq28. Like the MAGE genes located in Xq28, the MAGE-B genes are silent in normal tissues with the exception of testis. Like MAGE-1, 2, 3, 4, 6 and 12 (HGMW-approved symbols MAGEA1, 2, 3, 4, 6, and 12), genes MAGE-B1 and MAGE-B2 are expressed in a significant fraction of tumors of various histological types. The transcription of MAGE-B1 and MAGE-B2 can be induced by 5-aza-2'-deoxycytidine, suggesting that the activation of these genes in tumors results from a demethylation process. (C) 1997 Academic Press.
引用
收藏
页码:397 / 408
页数:12
相关论文
共 48 条
[1]   A DOSAGE SENSITIVE LOCUS AT CHROMOSOME XP21 IS INVOLVED IN MALE TO FEMALE SEX REVERSAL [J].
BARDONI, B ;
ZANARIA, E ;
GUIOLI, S ;
FLORIDIA, G ;
WORLEY, KC ;
TONINI, G ;
FERRANTE, E ;
CHIUMELLO, G ;
MCCABE, ERB ;
FRACCARO, M ;
ZUFFARDI, O ;
CAMERINO, G .
NATURE GENETICS, 1994, 7 (04) :497-501
[2]  
BOON T, 1994, ANNU REV IMMUNOL, V12, P337, DOI 10.1146/annurev.iy.12.040194.002005
[3]  
BOON T, 1995, CLIN ONCOLOGY, P90
[4]   EXPRESSION OF MAGE GENES IN PRIMARY AND METASTATIC CUTANEOUS MELANOMA [J].
BRASSEUR, F ;
RIMOLDI, D ;
LIENARD, D ;
LETHE, B ;
CARREL, S ;
ARIENTI, F ;
SUTER, L ;
VANWIJCK, R ;
BOURLOND, A ;
HUMBLET, Y ;
VACCA, A ;
CONESE, M ;
LAHAYE, T ;
DEGIOVANNI, G ;
DERAEMAECKER, R ;
BEAUDUIN, M ;
SASTRE, X ;
SALAMON, E ;
DRENO, B ;
JAGER, E ;
KNUTH, A ;
CHEVREAU, C ;
SUCIU, S ;
LACHAPELLE, JM ;
POUILLART, P ;
PARMIANI, G ;
LEJEUNE, F ;
CEROTTINI, JC ;
BOON, T ;
MARCHAND, M .
INTERNATIONAL JOURNAL OF CANCER, 1995, 63 (03) :375-380
[5]   HUMAN GENE MAGE-1, WHICH CODES FOR A TUMOR-REJECTION ANTIGEN, IS EXPRESSED BY SOME BREAST-TUMORS [J].
BRASSEUR, F ;
MARCHAND, M ;
VANWIJCK, R ;
HERIN, M ;
LETHE, B ;
CHOMEZ, P ;
BOON, T .
INTERNATIONAL JOURNAL OF CANCER, 1992, 52 (05) :839-841
[6]   ALTERATIONS IN DNA METHYLATION MAY PLAY A VARIETY OF ROLES IN CARCINOGENESIS [J].
COUNTS, JL ;
GOODMAN, JI .
CELL, 1995, 83 (01) :13-15
[7]   A FAMILY OF RAPIDLY EVOLVING GENES FROM THE SEX REVERSAL CRITICAL REGION IN XP21 [J].
DABOVIC, B ;
ZANARIA, E ;
BARDONI, B ;
LISA, A ;
BORDIGNON, C ;
RUSSO, V ;
MATESSI, C ;
TRAVERSARI, C ;
CAMERINO, G .
MAMMALIAN GENOME, 1995, 6 (09) :571-580
[8]  
DAVIS LG, 1986, BASIC METHODS MOL BI, P130
[9]   STRUCTURE, CHROMOSOMAL LOCATION, AND EXPRESSION PATTERN OF 3 MOUSE GENES HOMOLOGOUS TO THE HUMAN MAGE GENES [J].
DEBACKER, O ;
VERHEYDEN, AM ;
MARTIN, B ;
GODELAINE, D ;
DEPLAEN, E ;
BRASSEUR, R ;
AVNER, P ;
BOON, T .
GENOMICS, 1995, 28 (01) :74-83
[10]  
DELOOF H, 1986, P NATL ACAD SCI USA, V83, P2295