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细胞原癌基因myc已通过逆转录病毒插入而被激活的小鼠T淋巴瘤。

Murine T lymphomas in which the cellular myc oncogene has been activated by retroviral insertion.

作者信息

Corcoran L M, Adams J M, Dunn A R, Cory S

出版信息

Cell. 1984 May;37(1):113-22. doi: 10.1016/0092-8674(84)90306-4.

Abstract

The myc oncogene is implicated here in T lymphocyte neoplasia. Cloning revealed a retroviral insert 0.7-1.3 kb 5' to c-myc in two T lymphomas induced by Soule murine leukemia virus and in a spontaneous T lymphoma ( Tikaut ) of an AKR mouse, a strain in which leukemogenesis involves recombinant retroviruses (MCF viruses). The tumor c-myc mRNAs appear normal but their level is approximately 5-fold higher than in most T lymphomas lacking c-myc rearrangement. Since each insert would be transcribed away from c-myc, its activation cannot involve the promoter of the long terminal repeat (LTR) but could reflect an enhancer, like that demonstrated within the Soule LTR. The Tikaut provirus has an MCF-like recombinant env gene and LTR sequence. MCF-like inserts were found near c-myc in seven of 31 other AKR T lymphomas; two lie 3' to c-myc and the five upstream are oriented away from c-myc. We conclude that a quarter of retrovirus-induced T lymphomas involve activation of c-myc, probably via the LTR enhancer.

摘要

原癌基因myc在此与T淋巴细胞肿瘤形成有关。克隆显示,在Soule鼠白血病病毒诱导的两例T淋巴瘤以及AKR小鼠(该品系白血病发生涉及重组逆转录病毒(MCF病毒))的一例自发T淋巴瘤(Tikaut)中,在c-myc 5'端0.7 - 1.3 kb处有一个逆转录病毒插入片段。肿瘤中的c-myc mRNA看似正常,但其水平比大多数缺乏c-myc重排的T淋巴瘤大约高5倍。由于每个插入片段都会从c-myc转录,其激活不可能涉及长末端重复序列(LTR)的启动子,但可能反映了一个增强子,就像在Soule LTR中所证实的那样。Tikaut前病毒具有一个MCF样重组env基因和LTR序列。在31例其他AKR T淋巴瘤中的7例中,在c-myc附近发现了MCF样插入片段;其中两个位于c-myc的3'端,上游的五个则远离c-myc定向排列。我们得出结论,四分之一的逆转录病毒诱导的T淋巴瘤涉及c-myc的激活,可能是通过LTR增强子实现的。

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