Tolias P P, DuBow M S
EMBO J. 1985 Nov;4(11):3031-7. doi: 10.1002/j.1460-2075.1985.tb04040.x.
From the transposable Mu-like bacteriophage D108 we have cloned the ner gene under the control of the lac UV5 promoter in the expression vector pOP95-15. The recombinant plasmid, pPT011, overproduced the 8-kd D108 ner protein (visualized by in vitro-coupled transcription-translation) and served as a substrate for DNA sequencing of the D108 ner gene. The ner protein of D108 was found to be 48% homologous to the Mu ner protein, though the DNA sequences that encode these proteins are quite divergent. We used the retardation of migration of 32P-labelled DNA restriction fragments by ner-containing crude protein extracts in polyacrylamide gels (band competition assay) to determine which DNA restriction fragment(s) contained the ner-binding sites. DNA footprinting using crude extracts physically identified the 47-bp DNA sequence that the ner protein was interacting with in the D108 early gene regulatory region. This sequence is located 10 bp downstream from the presumed D108 early gene transcription initiation site. Therefore, by binding strongly to this 47-bp DNA sequence, the D108 ner protein can regulate D108 early gene transcription.
我们从类转座Mu噬菌体D108中,在表达载体pOP95 - 15的lac UV5启动子控制下克隆了ner基因。重组质粒pPT011过量表达8kd的D108 ner蛋白(通过体外偶联转录-翻译观察到),并作为D108 ner基因DNA测序的底物。尽管编码这些蛋白的DNA序列差异很大,但发现D108的ner蛋白与Mu ner蛋白有48%的同源性。我们利用含ner的粗蛋白提取物在聚丙烯酰胺凝胶中对32P标记的DNA限制片段迁移的阻滞作用(条带竞争试验)来确定哪些DNA限制片段含有ner结合位点。使用粗提取物进行的DNA足迹分析从物理上确定了在D108早期基因调控区域中ner蛋白与之相互作用的47bp DNA序列。该序列位于推测的D108早期基因转录起始位点下游10bp处。因此,通过与这47bp DNA序列强烈结合,D108 ner蛋白可以调控D108早期基因转录。