Hawkins A R
Department of Biochemistry, University of Leicester, UK.
Curr Genet. 1987;11(6-7):491-8. doi: 10.1007/BF00384611.
The physical positions of the DNA sequences encoding the five consecutive enzyme activities required to metabolise 3-deoxy-D-arabino-heptulosonic acid-7-phosphate to 5-enolpyruvyl-shikimate-3phosphate, which are encoded by the A. nidulans Arom polypeptide have been determined. Subfragments of the Arom locus encoding EPSP synthase and 3-dehydroquinase have been expressed in appropriate E. coli aro mutants. The DNA sequence of the A. nidulans Arom locus has been shown to have homology with the corresponding unlinked E. coli aro loci strongly suggesting (I) divergent evolution from common ancestral sequences and (II) that the complex A. nidulans Arom locus arose by multiple gene fusion. The DNA and protein sequence of the two 3-dehydroquinase isoenzymes of A. nidulans share no homology, strongly indicating separate phylogenetic origins and their convergent evolution. The 5' and 3' non-translated DNA sequence of the A. nidulans Arom locus is presented along with the presumed sites for transcription initiation and polyadenylation determined by S1 nuclease protection experiments.
编码将7-磷酸-3-脱氧-D-阿拉伯庚酮糖酸代谢为5-烯醇丙酮酸莽草酸-3-磷酸所需的5种连续酶活性的DNA序列的物理位置已被确定,这些序列由构巢曲霉Arom多肽编码。编码5-烯醇丙酮酸莽草酸-3-磷酸合酶和3-脱氢奎尼酸酶的Arom基因座的亚片段已在合适的大肠杆菌aro突变体中表达。已证明构巢曲霉Arom基因座的DNA序列与相应的不连锁的大肠杆菌aro基因座具有同源性,这强烈表明(I)从共同祖先序列的趋异进化,以及(II)复杂的构巢曲霉Arom基因座是通过多个基因融合产生的。构巢曲霉的两种3-脱氢奎尼酸同工酶的DNA和蛋白质序列没有同源性,这强烈表明它们有独立的系统发育起源和趋同进化。本文给出了构巢曲霉Arom基因座的5'和3'非翻译DNA序列,以及通过S1核酸酶保护实验确定的假定转录起始位点和聚腺苷酸化位点。