Morris D W, Dutra J C
Department of Medical Pathology, University of California, Davis 95616, USA.
Virology. 1997 Nov 10;238(1):161-5. doi: 10.1006/viro.1997.8794.
The Fgf-3 protooncogene (previously called int-2) is a target of proviral insertion mutations in mammary tumors induced by the mouse mammary tumor virus (MMTV). These insertion mutations result in the transcriptional activation of Fgf-3, which is not normally expressed in the adult mammary gland. Previous mapping studies of numerous Fgf-3 insertion mutations have failed to reveal any provirus integrations within the gene coding region. This finding is consistent with the hypothesis that oncogenesis occurs in this system as a consequence of up-regulation of Fgf-3 transcription, rather than from alterations of the gene product. During an analysis of a new cohort of tumors from the WXG-2 mouse strain, a breast tumor was identified which had a MMTV provirus integrated 24 bp upstream of the Fgf-3 stop codon. This insertion mutation generated a fusion transcript which was readily detectable in tumor RNA by RT-PCR. The predicted protein product of this fusion transcript is missing 8 aa of native sequence and contains an additional 8 aa of cryptic MMTV-encoded sequence. These data document the first exception to the generalization that the Fgf-3 coding region is not disrupted by MMTV insertion mutation.
Fgf-3原癌基因(以前称为int-2)是小鼠乳腺肿瘤病毒(MMTV)诱导的乳腺肿瘤中前病毒插入突变的靶点。这些插入突变导致Fgf-3转录激活,而Fgf-3在成年乳腺中通常不表达。先前对众多Fgf-3插入突变的定位研究未能揭示基因编码区内有任何前病毒整合。这一发现与以下假设一致,即在该系统中肿瘤发生是Fgf-3转录上调的结果,而非基因产物改变所致。在对来自WXG-2小鼠品系的一组新肿瘤进行分析时,鉴定出一个乳腺肿瘤,其MMTV前病毒整合在Fgf-3终止密码子上游24 bp处。这种插入突变产生了一个融合转录本,通过RT-PCR在肿瘤RNA中很容易检测到。该融合转录本的预测蛋白质产物缺失了8个天然序列的氨基酸,并包含另外8个MMTV编码的隐蔽序列的氨基酸。这些数据证明了Fgf-3编码区不会因MMTV插入突变而被破坏这一普遍观点的第一个例外情况。