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噬菌体T4晚期基因表达:重叠启动子指导基板基因簇的反向转录。

Bacteriophage T4 late gene expression: overlapping promoters direct divergent transcription of the base plate gene cluster.

作者信息

Scarlato V, Storlazzi A, Gargano S, Cascino A

机构信息

International Institute of Genetics and Biophysics, Naples, Italy.

出版信息

Virology. 1989 Aug;171(2):475-83. doi: 10.1016/0042-6822(89)90617-x.

Abstract

Eight 5' ends of RNA molecules which encompass the bacteriophage T4 base plate late genes 51 to 26 region have been mapped by S1 nuclease protection and reverse transcription within a 246-bp DNA segment. Two of eight 5' ends are initiated at two absolutely conserved late promoter sites, P51 and P26a, that direct RNA synthesis on opposite strands. These two promoters share four of eight promoter sequence base pairs. A third 5' end arises from another promoter, P26b, which shows one base pair mismatch with respect to the absolutely conserved -10 sequence. All the other 5' ends arise from RNA processing and/or degradation. Since no other late transcription promoter sites were found within the base plate cluster sequence, we propose that the two overlapping late promoters, P51 and P26a, direct the expression of the T4 base plate gene cluster, included between map coordinates 114,000 and 121,038: P51 directs the transcription of genes 51, 27, 28, 29, 48, and 54 on the rDNA strand and P26a the transcription of genes 26 and 25 on the /DNA strand. This peculiar promoter configuration might account for the low level of transcription of these late genes.

摘要

通过S1核酸酶保护和逆转录技术,在一段246bp的DNA片段内绘制了8个RNA分子的5'末端图谱,这些RNA分子包含噬菌体T4基板晚期基因51至26区域。8个5'末端中的两个起始于两个绝对保守的晚期启动子位点,P51和P26a,它们在相反的链上指导RNA合成。这两个启动子共享8个启动子序列碱基对中的4个。第三个5'末端来自另一个启动子P26b,它与绝对保守的-10序列有一个碱基对错配。所有其他5'末端都来自RNA加工和/或降解。由于在基板簇序列中未发现其他晚期转录启动子位点,我们提出两个重叠的晚期启动子P51和P26a指导T4基板基因簇的表达,该基因簇位于图谱坐标114,000和121,038之间:P51指导rDNA链上基因51、27、28、29、48和54的转录,P26a指导/DNA链上基因26和25的转录。这种特殊的启动子配置可能解释了这些晚期基因转录水平较低的原因。

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