Harbers K, Kuehn M, Delius H, Jaenisch R
Proc Natl Acad Sci U S A. 1984 Mar;81(5):1504-8. doi: 10.1073/pnas.81.5.1504.
Integration of the Moloney murine leukemia virus (M-MuLV) into the germ line of Mov-13 mice blocked formation of stable alpha 1(I) collagen mRNA and led to an embryonic lethal mutation. A 14-kilobase fragment representing the integration site of the virus was molecularly cloned and identified as the alpha 1(I) collagen gene. Sequence and nuclease S1 mapping analyses were performed to characterize the position of the proviral genome in relation to the transcriptional map of the mutated gene. The results indicated that the virus has inserted into the first intron 19 base pairs downstream of the intron/exon boundary. Sequence comparison showed a striking homology of exon sequences and sequences up to 215 base pairs upstream of the mRNA start between the mouse and the human alpha 1(I) collagen gene. This indicates that the sequences upstream of the mRNA start are highly conserved during evolution, suggesting that this region has an important role in the control of tissue-specific collagen expression.
莫洛尼鼠白血病病毒(M-MuLV)整合到Mov-13小鼠的种系中,阻断了稳定的α1(I)型胶原mRNA的形成,并导致胚胎致死性突变。代表病毒整合位点的一个14千碱基片段被进行分子克隆,并被鉴定为α1(I)型胶原基因。进行了序列分析和核酸酶S1图谱分析,以确定前病毒基因组相对于突变基因转录图谱的位置。结果表明,病毒插入到内含子/外显子边界下游19个碱基对的第一个内含子中。序列比较显示,小鼠和人类α1(I)型胶原基因的外显子序列以及mRNA起始位点上游多达215个碱基对的序列具有显著的同源性。这表明mRNA起始位点上游的序列在进化过程中高度保守,提示该区域在组织特异性胶原表达的调控中具有重要作用。