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多头绒泡菌肌动蛋白基因座ardA的结构:非回文序列导致λ噬菌体无法存活及recA非依赖性缺失。

Structure of Physarum actin gene locus ardA: a nonpalindromic sequence causes inviability of phage lambda and recA-independent deletions.

作者信息

Nader W F, Isenberg G, Sauer H W

出版信息

Gene. 1986;48(1):133-44. doi: 10.1016/0378-1119(86)90359-8.

Abstract

Previously we reported that approx. 80% of the genome from the plasmodial slime mold Physarum polycephalum, including all the actin genes, can be cloned only in recBC- sbcB- Escherichia coli hosts [Nader et al., Proc. Natl. Acad. Sci. USA 82 (1985) 2698-2702]. We have now sequenced the actin gene locus ardA. The nucleotide sequence of its coding region is flanked by the typical putative regulatory sequences for transcription initiation and polyadenylation. The coding region is interrupted by five introns, all located at novel positions with regard to those of previously analysed actin genes. Within the ardA gene we have located a 360-bp fragment which comprises exon V and parts of its flanking introns. This region suppresses plaque formation of recombinant lambda phages and causes recA-independent deletions in phages and plasmids. In contrast to our previous hypothesis, this sequence is not a DNA palindrome, but consists of five (dA) X (dT)- and (dG) X (dC)-homopolymers. Both termination of replication and partial unwinding of duplex DNA under torsional stress were detected within the unstable 360-bp region in vitro.

摘要

此前我们报道过,多头绒泡菌的约80%基因组,包括所有肌动蛋白基因,只能在recBC - sbcB -的大肠杆菌宿主中克隆出来[Nader等人,《美国国家科学院院刊》82 (1985) 2698 - 2702]。我们现已对肌动蛋白基因位点ardA进行了测序。其编码区的核苷酸序列两侧是典型的推测转录起始和聚腺苷酸化调控序列。编码区被五个内含子打断,这些内含子相对于之前分析过的肌动蛋白基因而言,均位于新的位置。在ardA基因内,我们定位到一个360 bp的片段,它包含外显子V及其侧翼内含子的部分序列。该区域会抑制重组λ噬菌体的噬菌斑形成,并导致噬菌体和质粒中出现不依赖recA的缺失。与我们之前的假设相反,该序列不是DNA回文序列,而是由五个(dA)X(dT)和(dG)X(dC)同聚物组成。在体外,在不稳定的360 bp区域内检测到了复制终止和双链DNA在扭转应力下的部分解旋。

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