Volff J N, Eichenseer C, Viell P, Piendl W, Altenbuchner J
Institut für Industrielle Genetik, Universität Stuttgart, Germany.
Mol Microbiol. 1996 Sep;21(5):1037-47. doi: 10.1046/j.1365-2958.1996.761428.x.
The amplifiable unit of DNA no. 1 (AUD1) of Streptomyces lividans consists of three 1 kb repeats (left direct repeat, LDR; middle direct repeat, MDR; and the slightly different right direct repeat, RDR) and two 4.7 kb repeats alternately arranged in identical orientation to each other. Both 4.7 kb repeats have been sequenced. They are identical and contain one open reading frame (orf4.7). The deduced amino acid sequence has a low similarity to chitinases, and two amino acid repeats present high similarities to fibronectin type III modules. Sequencing had previously shown that the ORF corresponding to each 1 kb repeat encodes a putative DNA-binding protein. Crude extracts of Escherichia coli overexpressing the orfRDR-encoded protein and of S. lividans Jni1, having a high amplification of AUD1 and therefore orfMDR, were used in gel retardation assays. The orfRDR- and probably the orfMDR-encoded proteins can bind to an imperfect palindromic sequence upstream from MDR and RDR and to another sequence downstream from RDR. An extrachromosomal DNA amplification system was constructed containing different combinations of the sequences composing AUD1. In mutants having a deletion of the chromosomal AUD1, the 4.7 kb repeats could be reduced in size, mutated or replaced by E. coli DNA without altering the ability to amplify when RDR was present. Therefore, the only function of the 4.7 kb repeats in amplification is to provide directly repeated DNA sequences. When RDR was lacking or mutated, no amplification was observed. This strongly suggests that the DNA-binding protein encoded by orfRDR is required for AUD1 amplification.
淡紫链霉菌DNA 1号可扩增单元(AUD1)由三个1 kb重复序列(左侧同向重复序列,LDR;中间同向重复序列,MDR;以及略有不同的右侧同向重复序列,RDR)和两个4.7 kb重复序列交替排列而成,彼此方向相同。两个4.7 kb重复序列均已测序。它们完全相同,包含一个开放阅读框(orf4.7)。推导的氨基酸序列与几丁质酶的相似性较低,两个氨基酸重复序列与纤连蛋白III型模块具有高度相似性。此前测序表明,对应于每个1 kb重复序列的开放阅读框编码一种假定的DNA结合蛋白。凝胶阻滞试验使用了过表达orfRDR编码蛋白的大肠杆菌粗提物,以及具有高扩增性AUD1(因而具有orfMDR)的淡紫链霉菌Jni1粗提物。orfRDR编码的蛋白以及可能orfMDR编码的蛋白能够结合到MDR和RDR上游的一个不完全回文序列以及RDR下游的另一个序列上。构建了一个包含构成AUD1的不同序列组合的染色体外DNA扩增系统。在染色体AUD1缺失的突变体中,当存在RDR时,4.7 kb重复序列的大小可以减小、发生突变或被大肠杆菌DNA取代,而不改变扩增能力。因此,4.7 kb重复序列在扩增中的唯一功能是提供直接重复的DNA序列。当RDR缺失或发生突变时,未观察到扩增现象。这有力地表明,orfRDR编码的DNA结合蛋白是AUD1扩增所必需的。