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前病毒插入Tpl-1(一种与Ets-1相关的致癌基因)与莫洛尼鼠白血病病毒诱导的大鼠胸腺淋巴瘤的肿瘤进展相关。

Provirus insertion in Tpl-1, an Ets-1-related oncogene, is associated with tumor progression in Moloney murine leukemia virus-induced rat thymic lymphomas.

作者信息

Bear S E, Bellacosa A, Lazo P A, Jenkins N A, Copeland N G, Hanson C, Levan G, Tsichlis P N

机构信息

Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, PA 19111.

出版信息

Proc Natl Acad Sci U S A. 1989 Oct;86(19):7495-9. doi: 10.1073/pnas.86.19.7495.

Abstract

T-cell lymphomas induced in rats by Moloney murine leukemia virus acquire increasing numbers of proviruses in their genome during tumor progression in vivo and passage of tumor cells in vitro. To determine whether the proviruses progressively acquired during tumor progression play a causal role in this process, we cloned one of them from a cell line derived from the primary tumor 2772. A probe from the cellular DNA flanking the provirus was used to analyze 79 DNA samples from primary tumor tissues of 28 tumor-bearing rats and 80 DNA samples from 30 independent tumor cell lines. This analysis revealed a rearrangement in this region in the primary tumor derived from the thymus of one animal but not in a clone of the same tumor segregating in the spleen. Of the cell line DNA samples, three carried a provirus in this region. Two of these integration events had occurred independently in two clonally related sublines derived from tumor 2772, and they were followed by rapid selection in culture. On the basis of these findings this locus was named Tpl-1 (tumor progression locus 1). The Tpl-1 locus was mapped to rat chromosome 8 and to mouse chromosome 9 at a genetic distance of 1.2 +/- 0.9 centimorgans from the Ets-1 protooncogene. Although the genetic distance between Tpl-1 and Ets-1 indicates that they are different genes, analysis of Tpl-1 cDNA clones revealed that the two are closely related.

摘要

莫洛尼鼠白血病病毒在大鼠体内诱发的T细胞淋巴瘤,在体内肿瘤进展过程以及肿瘤细胞体外传代过程中,其基因组中的前病毒数量不断增加。为了确定肿瘤进展过程中逐渐获得的前病毒是否在此过程中起因果作用,我们从源自原发性肿瘤2772的细胞系中克隆了其中一个。用前病毒侧翼细胞DNA的探针分析了28只荷瘤大鼠原发性肿瘤组织的79个DNA样本,以及30个独立肿瘤细胞系的80个DNA样本。该分析揭示,在一只动物胸腺来源的原发性肿瘤肿瘤中该区域存在重排,但在同一肿瘤在脾脏中分离出的克隆中未发现。在细胞系DNA样本中,有三个在该区域携带前病毒。其中两个整合事件独立发生在源自肿瘤2772的两个克隆相关亚系中,随后在培养中被快速选择。基于这些发现,该基因座被命名为Tpl-1(肿瘤进展基因座1)。Tpl-1基因座被定位到大鼠8号染色体以及小鼠9号染色体上,与Ets-1原癌基因的遗传距离为1.2±0.9厘摩。尽管Tpl-1和Ets-1之间的遗传距离表明它们是不同的基因,但对Tpl-1 cDNA克隆的分析显示二者密切相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/451d/298091/d044109f68ce/pnas00286-0206-a.jpg

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