Stegalkina S S, Guerrero A, Walton K D, Liu X, Robinson G W, Hennighausen L
Laboratory of Genetics and Physiology, National Institute of Diabetes, and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
J Virol. 1999 Oct;73(10):8669-76. doi: 10.1128/JVI.73.10.8669-8676.1999.
The enhancer within the long terminal repeats (LTRs) of acquired somatic mouse mammary tumor viruses (MMTV) can activate juxtaposed genes and induce mammary tumors. In contrast, germ line proviral MMTV genomes are integrated in the host genome and considered to be genetically confined transcription units. Here we demonstrate that transcription initiated in an MMTV provirus proceeds into flanking host sequences. We discovered multiple polyadenylated transcripts which are induced in Stat5a null mice. These range from 1.5 kb to more than 8 kb and are specifically expressed in mammary tissue from pregnant and lactating mice from the 129 but not C57BL/6 strain. The RNAs emanate from both LTRs of the endogenous MTV-3 provirus on chromosome 11 and proceed at least 10 kb into the juxtaposed genomic territory. Transcripts originating in the 5' LTR splice from the native splice site within the MMTV envelope gene into at least six exons, three of which contain functional internal splice sites. The combination of alternative splicing and the use of several polyadenylation sites ensure the generation of multiple transcripts. To date no significant open reading frame has been discovered. Furthermore, we demonstrate that transcription from the MMTV 5' LTR is highly active in the absence of Stat5a, a transcription factor that had been shown previously to be required for transcription from the MMTV LTR.
获得性体细胞小鼠乳腺肿瘤病毒(MMTV)长末端重复序列(LTR)中的增强子可激活相邻基因并诱发乳腺肿瘤。相比之下,种系前病毒MMTV基因组整合于宿主基因组中,被认为是基因受限的转录单位。在此我们证明,MMTV前病毒启动的转录会延伸至侧翼宿主序列。我们发现了多种在Stat5a基因敲除小鼠中被诱导产生的多聚腺苷酸化转录本。这些转录本长度从1.5 kb到超过8 kb不等,且在来自129品系而非C57BL/6品系的怀孕和哺乳期小鼠的乳腺组织中特异性表达。这些RNA源自11号染色体上内源性MTV - 3前病毒的两个LTR,并至少延伸10 kb进入相邻的基因组区域。源自5' LTR的转录本从MMTV包膜基因内的天然剪接位点剪接成至少六个外显子,其中三个含有功能性内部剪接位点。可变剪接与多个聚腺苷酸化位点的使用相结合确保了多种转录本的产生。迄今为止尚未发现明显的开放阅读框。此外,我们证明在缺乏Stat5a的情况下,MMTV 5' LTR的转录高度活跃,Stat5a是一种先前已证明MMTV LTR转录所必需的转录因子。