CLONING AND ANALYSIS OF MAGE-1-RELATED GENES

被引:20
作者
DING, M
BECK, RJ
KELLER, CJ
FENTON, RG
机构
[1] NCI,FREDERICK CANC RES & DEV CTR,CLIN RES BRANCH,BIOL RESPONSE MODIFIERS PROGRAM,FREDERICK,MD 21702
[2] NCI,FREDERICK CANC RES & DEV CTR,DYNCORP,PROGRAM RESOURCES INC,BIOL CARCINOGENESIS & DEV P,FREDERICK,MD 21702
关键词
D O I
10.1006/bbrc.1994.1963
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The spectrum of MAGE gene expression in the human melanoma cell line DM150 was examined using reverse transcription polymerase chain reaction and cDNA cloning. We have examined isolated five full-length cDNAs from DM150 which were identified as MAGE-1, MAGE-3, MAGE-12 and two previously undescribed MAGE, MAGE-3b and MAGE-X2. DNA sequence analysis of the coding regions of the MAGE-3b and MAGE-X2 genes revealed 83% and 88% identity with MAGE-1, while MAGE-3b was 98% homologous with the full length MAGE-3 clone. The predicted amino acid sequences of MAGE-X2 and MAGE-3b contain consensus HLA-A1 peptide binding motifs, suggesting that, like MAGE-1, they may code for tumor- associated antigens. In addition, a nonamer peptide encoded by both the MAGE-3 and MAGE-12 genes was shown by direct binding studies to contain an aggretope for HLA-A2. (C) 1994 Academic Press, Inc.
引用
收藏
页码:549 / 555
页数:7
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