Kordon E C, Smith G H, Callahan R, Gallahan D
Laboratory of Tumor Immunology and Biology, National Cancer Institute, Bethesda, Maryland 20892, USA.
J Virol. 1995 Dec;69(12):8066-9. doi: 10.1128/JVI.69.12.8066-8069.1995.
In a mouse mammary tumor model system in which carcinogenic progression can be investigated, we have found a unique mutation of Int-3 associated with progression from premalignant lobular hyperplasia to tumor. Sequence analysis of the rearranged fragment revealed an insertion of an intracisternal type A particle (IAP) within the Int-3 gene. Int-3 is mutated frequently in mouse mammary tumor virus (MMTV)-induced mammary tumors by insertion of MMTV proviral DNA into this intragenic region. In these mutations, the insertion produces a chimeric Int-3 transcript encoding the cytoplasmic portion of the Int-3 protein driven by the MMTV long terminal repeat promoter. In this case, the IAP DNA was inserted in the opposite transcriptional orientation relative to Int-3; nevertheless, a similar chimeric RNA transcript driven by a cryptic promoter in the oppositely oriented 5' IAP long terminal repeat was generated. This is the first demonstration that an insertional mutation unrelated to MMTV activates an Int gene commonly associated with mammary tumorigenesis.
在一个能够研究致癌进展的小鼠乳腺肿瘤模型系统中,我们发现了Int-3的一种独特突变,该突变与从癌前小叶增生到肿瘤的进展相关。对重排片段的序列分析显示,在Int-3基因内插入了一个A型脑内池样颗粒(IAP)。在小鼠乳腺肿瘤病毒(MMTV)诱导的乳腺肿瘤中,Int-3经常因MMTV前病毒DNA插入该基因区域而发生突变。在这些突变中,插入产生一种嵌合Int-3转录本,其由MMTV长末端重复启动子驱动,编码Int-3蛋白的胞质部分。在这种情况下,IAP DNA以相对于Int-3相反的转录方向插入;然而,由反向定向的5'IAP长末端重复序列中的一个隐蔽启动子驱动,产生了一种类似的嵌合RNA转录本。这是首次证明与MMTV无关的插入突变激活了一个通常与乳腺肿瘤发生相关的Int基因。