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首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >Transcriptional regulation of pWW0 transfer genes in Pseudomonas putida KT2440.
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Transcriptional regulation of pWW0 transfer genes in Pseudomonas putida KT2440.

机译:恶臭假单胞菌KT2440中pWW0转移基因的转录调控。

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The conjugative IncP-9 plasmid pWW0 (TOL) carries transfer genes, many of whose functions can be predicted from sequence similarities to the well-studied IncW and IncP-1 plasmids, and that are clustered with the replication and maintenance genes of the plasmid core. In this study we show that the IncP-9 transfer genes are transcribed from at least three promoter regions. The promoters for traA and traD act divergently from the region found to encode the origin of transfer, oriT. These promoters regulate expression of traA, B, and perhaps traC in one direction and traD in the other, all of whose gene products are predicted to be involved in relaxasome formation and DNA processing during transfer, and they are repressed by TraA. The third promoter region, upstream of mpfR, is responsible for transcription of mpfR and mpfA to mpfJ, encoding proteins involved in mating pair formation. Transcription from this region is negatively autoregulated by MpfR. Thus the pWW0 transfer genes, like those of the IncP-1 plasmids, are expressed at all times, but kept in control by a negative feed back loop to limit the metabolic burden on the host. Although many of the related mating pair formation systems are, as in pWW0, transcribed divergently from an operon for replication and/or stable inheritance functions, MpfR is not related to the known regulatory proteins of these other transfer systems outside those of the IncP-9 family and indeed the regulators tend to be specific for each plasmid family. This suggests that the general pattern of genetic organisation exhibited by these systems has arisen a number of times independently and must therefore be highly favourable to plasmid survival and spread.
机译:结合型IncP-9质粒pWW0(TOL)带有转移基因,其许多功能可以从与研究得很好的IncW和IncP-1质粒的序列相似性预测出来,并与质粒核心的复制和维持基因聚集在一起。在这项研究中,我们显示了从至少三个启动子区域转录的IncP-9转移基因。 traA和traD的启动子从发现的编码转移起点oriT的区域起着不同的作用。这些启动子在一个方向上调节traA,B也许在traC的表达,在另一个方向上调节traD的表达,据预测,所有这些基因的基因产物都在转移过程中参与了弛豫体的形成和DNA加工,并且被TraA抑制。 mpfR上游的第三个启动子区域负责将mpfR和mpfA转录为mpfJ,编码参与配对对形成的蛋白质。 MpfR负向调节该区域的转录。因此,pWW0转移基因(如IncP-1质粒的基因)始终表达,但通过负反馈回路保持控制,以限制宿主的代谢负担。尽管许多相关的配对对形成系统(如pWW0)从操纵子发散地转录,以实现复制和/或稳定的遗传功能,但MpfR与IncP-9以外的其他转移系统的已知调节蛋白无关家族,实际上调节子往往对每个质粒家族具有特异性。这表明这些系统展示的遗传组织的一般模式已经独立出现了许多次,因此必须对质粒的存活和传播高度有利。

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