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位于Xp21.3的人类MAGEB基因家族的两个成员在各种组织学起源的肿瘤中表达。

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

作者信息

Lurquin C, De Smet C, Brasseur F, Muscatelli F, Martelange V, De Plaen E, Brasseur R, Monaco A P, Boon T

机构信息

Ludwig Institute for Cancer Research, Brussels Branch, Belgium.

出版信息

Genomics. 1997 Dec 15;46(3):397-408. doi: 10.1006/geno.1997.5052.

Abstract

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.

摘要

MAGE家族基因指导自体溶细胞性T淋巴细胞识别的人类黑色素瘤肿瘤抗原的表达。12个密切相关的MAGE基因位于Xq28区域。这些基因在其编码区域具有60 - 98%的核苷酸同一性。先前已报道在Xp21.3区域存在同源基因。我们获得了该区域一段42kb片段的完整序列。它包含四个与MAGE相关的基因,我们提议将其命名为MAGE - B1、B2、B3和B4(HGMW批准的符号为MAGEB1、MAGEB2、MAGEB3和MAGEB4)。这些基因的编码区域具有66 - 81%的核苷酸同一性,与位于Xq28的MAGE基因的编码区域具有45 - 63%的同一性。与位于Xq28的MAGE基因一样,除睾丸外,MAGE - B基因在正常组织中是沉默的。与MAGE - 1、2、3、4、6和12(HGMW批准的符号为MAGEA1、2、3、4、6和12)一样,MAGE - B1和MAGE - B2基因在各种组织学类型的大部分肿瘤中表达。MAGE - B1和MAGE - B2的转录可被5 - 氮杂 - 2'-脱氧胞苷诱导,这表明这些基因在肿瘤中的激活是由去甲基化过程导致的。

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