Reddy C D, Reddy E P
Wistar Institute, Philadelphia, PA 19104.
Proc Natl Acad Sci U S A. 1989 Oct;86(19):7326-30. doi: 10.1073/pnas.86.19.7326.
The molecular mechanisms that modulate c-myb mRNA levels in hematopoietic cells appear to involve premature termination of transcription in the first intron of the gene. We have examined the DNA-protein interactions within the first intron of the c-myb gene and identified a 1.0-kilobase region that could be responsible for its transcriptional regulation. Using the mobility-shift assay, we show a direct correlation between the extent of sequence-specific protein binding to intron 1 DNA fragments, and c-myb mRNA levels in different cell types. During dimethyl sulfoxide-induced differentiation of mouse erythroleukemic cells, there was a dramatic decrease in these nuclear factors that correlated with the decrease in the levels of c-myb mRNA. Nucleotide sequence analysis and DNase I footprinting revealed the presence of putative regulatory elements that are implicated in the binding of these nuclear factors. We propose that binding of nuclear factors to the site of transcriptional pause could play an important role in the regulation of c-myb transcription.
调节造血细胞中c-myb mRNA水平的分子机制似乎涉及该基因第一个内含子中提前终止转录。我们已经研究了c-myb基因第一个内含子内的DNA-蛋白质相互作用,并确定了一个1.0千碱基区域,该区域可能负责其转录调控。使用迁移率变动分析,我们显示了序列特异性蛋白质与内含子1 DNA片段结合的程度与不同细胞类型中c-myb mRNA水平之间的直接相关性。在二甲基亚砜诱导的小鼠红白血病细胞分化过程中,这些核因子显著减少,这与c-myb mRNA水平的降低相关。核苷酸序列分析和DNase I足迹分析揭示了与这些核因子结合有关的假定调控元件的存在。我们提出,核因子与转录暂停位点的结合可能在c-myb转录调控中起重要作用。