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Non-canonical sequence elements in the promoter structure. Cluster analysis of promoters recognized by Escherichia coli RNA polymerase.

机译:启动子结构中的非规范序列元素。大肠杆菌RNA聚合酶识别的启动子的聚类分析。

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摘要

Nucleotide sequences of 441 promoters recognized by Escherichia coli RNA polymerase were subjected to a site-specific cluster analysis based on the hierarchical method of classification. Five regions permitting promoter subgrouping were identified. They are located at -54 +/- 4, -44 +/- 3, -35 +/- 3 (-35 element), -29 +/- 2 and -11 +/-4 (-10 element). Promoters were independently subgrouped on the basis of their sequence homology in each of these regions and typical sequence elements were determined. The putative functional significance of the revealed elements is discussed on the basis of available biochemical data. Those promoters that have a high degree of homology with the revealed sequence elements were selected as representatives of corresponding promoter groups and the presence of other sequence motifs in their structure was examined. Both positive and negative correlations in the presence of particular sequence motifs were observed; however, the degree of these interdependencies was not high in all cases, probably indicating that different combinations of the signal elements may create a promoter. The list of promoter sequences with the presence of different sequence elements is available on request by Email: ozoline@venus.iteb. serpukhov.su.
机译:基于分类的分级方法,对大肠杆菌RNA聚合酶识别的441个启动子的核苷酸序列进行位点特异性聚类分析。确定了五个允许启动子分组的区域。它们位于-54 +/- 4,-44 +/- 3,-35 +/- 3(-35元素),-29 +/- 2和-11 +/- 4(-10元素)。根据在这些区域中每个区域的序列同源性,将启动子独立地分组,并确定典型的序列元件。在现有的生化数据的基础上讨论了揭示元素的假定功能意义。选择与揭示的序列元件高度同源的那些启动子作为相应启动子基团的代表,并检查其结构中其他序列基序的存在。在存在特定序列基序的情况下,观察到正相关和负相关;然而,在所有情况下这些相互依赖性的程度都不高,这可能表明信号元件的不同组合可能产生启动子。存在不同序列元件的启动子序列列表可通过电子邮件索取:ozoline@venus.iteb。 serpukhov.su。

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