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Nucleotide Fluctuation of Radiation-Resistant Halobacterium sp. NRC-1 Single-Stranded DNA-Binding Protein (RPA) Genes

机译:耐辐射盐杆菌的核苷酸波动NRC-1单链DNA结合蛋白(RPA)基因

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The Single-Stranded DNA-Binding Protein (RPA) Genes in gamma ray radiation-resistant halophilic archaeon Halobacterium sp. NRC-1 were analyzed in terms of their nucleotide fluctuations. In an ATCG sequence, each base was assigned a number equal to its atomic number. The resulting numerical sequence was the basis of the statistical analysis in this study. Fractal analysis using the Higuchi method gave fractal dimensions of 2.04 and 2.06 for the gene sequences VNG2160 and VNG2162, respectively. The 16S rRNA sequence has a fractal dimension of 1.99. The dinucleotide Shannon entropy values were found to be negatively correlated with the observed fractal dimensions (R~2~ 0.992, N=3). Inclusion of Deinococcus radiodurans Rad-A in the regression analysis decreases the R2 slightly to 0.98 (N=4). A third VNG2163 RPA gene of unknown function but with up-regulation activity under irradiation was found to have a fractal dimension of 2.05 and a Shannon entropy of 3.77 bits. The above results are similar to those found in bacterial Deinococcus radiodurans and suggest that their high radiation resistance property would have favored selection of CpG dinucleotide pairs. The two transcription factors TbpD (VNG7114) and TfbA (VNG 2184) were also studied. Using VNG7114, VNG2184, and VNG2163; the regression analysis of fractal dimension versus Shannon entropy shows that R~2 ~ 0.997 for N =3. The VNG2163 unknown function may be related to the pathways with transcriptions closely regulated to sequences VNG7114 and VNG2184.
机译:耐γ射线辐射的嗜盐古细菌Halobacterium sp。中的单链DNA结合蛋白(RPA)基因。根据其核苷酸波动分析了NRC-1。在ATCG序列中,为每个碱基分配的编号等于其原子序数。所得的数值序列是本研究中统计分析的基础。使用Higuchi方法的分形分析对于基因序列VNG2160和VNG2162分别给出了2.04和2.06的分形维数。 16S rRNA序列的分形维数为1.99。发现二核苷酸香农熵值与观测分形维数呈负相关(R〜2〜0.992,N = 3)。在回归分析中加入放射杜鹃球菌Rad-A可使R2略微降低至0.98(N = 4)。发现功能未知但在辐照下具有上调活性的第三个VNG2163 RPA基因具有2.05的分形维数和3.77位的香农熵。以上结果与在细菌Deinococcus radiodurans中发现的结果相似,表明它们的高抗辐射性将有利于CpG二核苷酸对的选择。还研究了两个转录因子TbpD(VNG7114)和TfbA(VNG 2184)。使用VNG7114,VNG2184和VNG2163;分形维数与香农熵的回归分析表明,N = 3时,R〜2〜0.997。 VNG2163未知功能可能与转录密切相关的途径有关,该转录与序列VNG7114和VNG2184密切相关。

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