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铜绿假单胞菌中多基因系统转录调控黏液形成的组分algP和algQ的DNA序列及表达分析:algP含有多个正向重复序列。

DNA sequence and expression analysis of algP and algQ, components of the multigene system transcriptionally regulating mucoidy in Pseudomonas aeruginosa: algP contains multiple direct repeats.

作者信息

Konyecsni W M, Deretic V

机构信息

Department of Microbiology, University of Texas Health Science Center, San Antonio 78284-7758.

出版信息

J Bacteriol. 1990 May;172(5):2511-20. doi: 10.1128/jb.172.5.2511-2520.1990.

Abstract

The complete nucleotide sequence of a 3.2-kilobase-pair chromosomal region containing the algP and algQ genes was determined. The algQ gene encodes an acidic 18-kilodalton polypeptide required for transcriptional activation of the algD gene. The algD gene product catalyzes a critical step in alginate biosynthesis, and its overproduction is necessary for the emergence of mucoid Pseudomonas aeruginosa during chronic infections in cystic fibrosis. A novel genetic element, algP, was identified immediately downstream of algQ. This gene appears to act synergistically with algQ. Unlike a biosynthetic gene, algD, and another regulatory gene, algR, which undergo transcriptional activation in mucoid cells, both algP and algQ are equally transcribed in mucoid and nonmucoid isogenic strains of P. aeruginosa. The promoter regions of algP and algQ were mapped by using S1 nuclease protection analysis. The algQ promoter was also analyzed and showed activity in an in vitro transcriptional runoff assay with major RNA polymerase species from P. aeruginosa and Escherichia coli. The putative algQ and algP promoter sequences, unlike algD and algR, resemble sigma 70-utilized promoters from E. coli and appeared constitutively transcribed at a low level in P. aeruginosa. The algP gene has an unusual DNA sequence, with multiple direct repeats organized in six highly conserved, tandemly arranged, 75-base-pair (bp) units. At a lower level, this sequence had 45 degenerate repeats of 12 bp overlapping with the 75-bp repeats and extending beyond the region of 75-bp repeats. The algP repeats appeared important for the function of the algQ-algP regulatory region in maintaining mucoidy.

摘要

测定了包含algP和algQ基因的一个3.2千碱基对染色体区域的完整核苷酸序列。algQ基因编码一种酸性的18千道尔顿多肽,它是algD基因转录激活所必需的。algD基因产物催化藻酸盐生物合成中的关键步骤,其过量产生对于囊性纤维化慢性感染期间黏液型铜绿假单胞菌的出现是必要的。一个新的遗传元件algP在algQ的紧邻下游被鉴定出来。该基因似乎与algQ协同作用。与在黏液型细胞中经历转录激活的生物合成基因algD和另一个调控基因algR不同,algP和algQ在黏液型和非黏液型铜绿假单胞菌同基因菌株中均等量转录。通过S1核酸酶保护分析对algP和algQ的启动子区域进行了定位。还对algQ启动子进行了分析,结果显示在使用来自铜绿假单胞菌和大肠杆菌的主要RNA聚合酶种类进行的体外转录延伸试验中具有活性。推测的algQ和algP启动子序列与algD和algR不同,类似于来自大肠杆菌的利用σ70的启动子,并且在铜绿假单胞菌中以低水平组成型转录。algP基因具有不寻常的DNA序列,有多个直接重复序列,这些重复序列按六个高度保守的、串联排列的75碱基对(bp)单元组织。在较低水平上,该序列有45个12 bp的简并重复序列,与75 bp的重复序列重叠并延伸到75 bp重复序列区域之外。algP重复序列对于algQ - algP调控区域维持黏液性的功能似乎很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d97/208891/c4f832cf783b/jbacter00119-0330-a.jpg

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