Structural analysis of the rhlE gene of Escherichia coli.

Idengaku zasshi Pub Date : 1994-02-01 DOI:10.1266/jjg.69.1
H Ohmori
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引用次数: 23

Abstract

The E. coli chromosome is known to carry at least five genes, each of which codes for a "D-E-A-D" box protein that is presumed to possess an ATP-dependent RNA helicase activity. Four of such genes (srmB, deaD, dbpA and rhlB) were already mapped on the E. coli chromosome and their DNA sequences determined. We here report the complete nucleotide sequence of the remaining rhlE gene located at about 17.8 min on the E. coli genetic map. RhlE protein possesses all of the motifs (I to VI) conserved among prokaryotic and eukaryotic "D-E-A-D" proteins and has an arginine-rich carboxyl-terminal region. A null mutant of the rhlE gene was constructed by a new method with a ColE1 plasmid mutant that replicates in RNAse HI-deficient bacterial strains, but not in the wild-type strains. The delta rhlE mutant can grow normally, implying that the rhlE gene product is nonessential for bacterial cell growth.

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大肠杆菌rhlE基因的结构分析。
已知大肠杆菌染色体携带至少5个基因,每个基因编码一个“D-E-A-D”盒子蛋白,该蛋白被认为具有依赖atp的RNA解旋酶活性。其中四个基因(srmB、deaD、dbpA和rhlB)已经被定位到大肠杆菌染色体上,并确定了它们的DNA序列。我们在此报告了位于大肠杆菌遗传图谱上约17.8 min的剩余rhlE基因的完整核苷酸序列。RhlE蛋白具有原核和真核“D-E-A-D”蛋白中保守的所有基序(I至VI),并具有一个富含精氨酸的羧基末端区域。用ColE1质粒突变体构建了rhlE基因的零突变体,该突变体在RNAse - hi缺陷菌株中复制,而在野生型菌株中不复制。δ rhlE突变体可以正常生长,这意味着rhlE基因产物对细菌细胞生长不是必需的。
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