首页> 外文会议>Annual Meeting of the Japanese Association for Animal Cell Technology >TRANSCRIPTIONAL REGULATION MECHANISMS OF TELOMERASE REVERSE TRANSCRIPTASE GENE RESPONSIBLE FOR UBIQUITOUS EXPRESSION OF TELOMERASE IN MOUSE
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TRANSCRIPTIONAL REGULATION MECHANISMS OF TELOMERASE REVERSE TRANSCRIPTASE GENE RESPONSIBLE FOR UBIQUITOUS EXPRESSION OF TELOMERASE IN MOUSE

机译:端粒酶逆转录酶基因的转录调节机制,其对小鼠端粒酶普遍存在的逆转转录酶基因

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Telomerase is known to maintain the telomcre by avoiding the shortening of the telomere which normally occurs during end replication, thus granting immortality to cancer cells and stem cells. Telomerase activity is thought to be regulated mainly at the transcriptional level. Furthermore, the telomerase regulation mechanism is reported to be markedly different between human and mouse, Particularly, telomerase has been shown not to be expressed in normal human tissues, but abundant expression has beenshown to be expressed in all mouse tissues except in brain and muscle tissue. By using various deletion mutants of mouse telomerase reverse transcriptase (mTERT) promoter in promoter assay, we obtained result thai -200 to -178 bp from the iranslational start site confers a strong transcriptional activity in mTERT promoter, where NF-AT and v-Myb are expected to bind. Although v-Myb could not activate the promoter, NF-AT member proteins, especially NF-AT5 could activate the 5 tandem repeat of -200 to -178fused to luciferase gene (mTERT-EE). Furthermore, dominant negative mutants of NF-AT5 repressed promoter activity of mTERT-EE. These results demonstrate that NF-AT5 activates the mTERT promoter activity via binding to -200 to -178 region, which might confers the ubiquitous expression of mTERT.
机译:端粒酶是已知的,通过避免该端复制期间通常发生的端粒的缩短,从而给予不朽癌细胞维持telomcre和干细胞。端粒酶活性被认为是主要调控在转录水平。此外,端粒酶调节机制被报道为人类和小鼠之间显着不同,特别是,端粒酶已被证明不能在正常人组织中表达,但大量表达已经beenshown在所有的小鼠组织中表达,除了在脑和肌肉组织。在启动子分析通过使用鼠标的各种缺失突变体端粒酶逆转录酶(mTERT)启动子,我们从iranslational起始位点赋予在mTERT启动子,获得的结果泰-200到-178 bp的强烈的转录活性,其中NF-AT和v-Myb的预期结合。虽然V形的Myb不能激活的启动子,NF-AT成员蛋白,尤其是NF-AT5可以激活-200 5串联重复到-178fused到荧光素酶基因(mTERT-EE)。此外,NF-AT5的显性负突变体抑制mTERT-EE的启动子活性。这些结果表明,NF-AT5通过结合至-200到-178区域,这可能赋予mTERT的无处不在的表达激活mTERT启动子活性。

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