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正常细胞和莫洛尼鼠白血病病毒诱导的大鼠T细胞淋巴瘤中Tpl-2的基因组组织与表达:前病毒插入激活

Genomic organization and expression of Tpl-2 in normal cells and Moloney murine leukemia virus-induced rat T-cell lymphomas: activation by provirus insertion.

作者信息

Makris A, Patriotis C, Bear S E, Tsichlis P N

机构信息

Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.

出版信息

J Virol. 1993 Jul;67(7):4283-9. doi: 10.1128/JVI.67.7.4283-4289.1993.

Abstract

Tpl-2 is a gene encoding a protein kinase which is primarily expressed in normal spleen, thymus, and lung tissue and is activated by provirus insertion in Moloney murine leukemia virus-induced T-cell lymphomas during the late stages of oncogenesis. Tpl-2 is composed of eight exons and spans a 35-kb genomic DNA region. The provirus integrates reproducibly in the last intron and in the same transcriptional orientation as the Tpl-2 gene. This genetic change leads to the expression of enhanced steady-state levels of a truncated Tpl-2 RNA transcript which is predicted to encode a protein with an altered C-terminal domain. Tpl-2 is transcribed from two alternating promoters, P1 and P2. The RNA transcripts originating in the two promoters harbor different 5' untranslated regions derived from the alternate noncoding exons IA and IB. Utilization of the P2 promoter, which gives rise to exon IB containing Tpl-2 RNA transcripts, was detected primarily in tumor cells. The Tpl-2 protein was expressed in COS-1 cells as an N-terminal fusion with a 12-amino-acid hemagglutinin tag. Immunoprecipitation of transfected COS-1 cell lysates with antihemagglutinin or anti-Tpl-2 antibodies, followed by incubation with [gamma-32P]ATP, confirmed that Tpl-2 possesses protein kinase activity.

摘要

Tpl-2是一种编码蛋白激酶的基因,主要在正常脾脏、胸腺和肺组织中表达,在莫洛尼鼠白血病病毒诱导的T细胞淋巴瘤发生的晚期,通过前病毒插入而被激活。Tpl-2由八个外显子组成,跨越35kb的基因组DNA区域。前病毒可重复性地整合到最后一个内含子中,且转录方向与Tpl-2基因相同。这种基因变化导致截短的Tpl-2 RNA转录本的稳态水平增强,预计该转录本编码一种C末端结构域改变的蛋白质。Tpl-2从两个交替的启动子P1和P2转录。源自这两个启动子的RNA转录本具有不同的5'非翻译区,这些区域来自交替的非编码外显子IA和IB。主要在肿瘤细胞中检测到使用P2启动子产生含有外显子IB的Tpl-2 RNA转录本。Tpl-2蛋白在COS-1细胞中作为与12个氨基酸的血凝素标签的N末端融合蛋白表达。用抗血凝素或抗Tpl-2抗体对转染的COS-1细胞裂解物进行免疫沉淀,然后与[γ-32P]ATP孵育,证实Tpl-2具有蛋白激酶活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebf0/237798/bd7a38f00aca/jvirol00028-0600-a.jpg

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