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人类转录假基因序列碱基片段的分析研究

Analysis Research on Basic Group Fragment of Human Transcribed Pseudogene Sequences
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摘要 对人类201条转录假基因的2碱基片段、3碱基片段、4碱基片段、5碱基片段和6碱基片段进行了统计。发现所统计的碱基片段在相对频率小于2范围内的模式占总模式数的89%以上;长度较长的碱基片段(5碱基片段、6碱基片段)同三核苷酸碱基片段之间包含和被包含关系较明显;人类转录假基因序列里出现最多的碱基片段大多是由AG核组成的,稀有模式主要是以CG核组成的3碱基片段,这可能是因为转录假基因序列与其同源编码基因mRNA竞争去稳定蛋白所引起的;在人类转录假基因序列中每平均约26个碱基就有一个终止密码子模式(TAG、TAA和TGA),终止密码子的频繁出现可能是原功能基因编码区的一种容错机制。另外,进行了相对频率的统计分析,发现对于2碱基片段、3碱基片段、4碱基片段、5碱基片段和6碱基片段的研究是具有其统计意义的。 It has been carried on the statistics about 2 basic group fragments, 3 basic group fragments, 4 basic group fragments, 5 basic group fragments and 6 basic group fragments from the 201 human transcribed pseudogenes. The author found that the above 89% basic group fragments of the total are in the region of the relative frequency (RF)≤2 . It is quite obvious that the longer basic group fragments (5 basic group fragments, 6 basic group fragments ) are made up of the 3 basic group fragments. In the human transcribed-pseudogenic sequences the longer base elements mostly are composed by AG. And the rare pattern mainly has the 3 basic group fragments which is form of CG. This possibly is for as much as that the transcribed-pseudogenic sequence competes for the non-stable protein with mRNA of its homologous coding gene. Every approximate 26 basic groups have a termination-codon(TAG, TAA and TGA) equally in the human transcribed -pseudogenic sequences. This continual appearance possibly is the original functional genic coding region's fault-tolerant mechanism. In addition, we have carried on statistical analysis of RF, and discovered that the analysis research about 2 basic group fragments, 3 basic group fragments, 4 basic group fragments, 5 basic group fragments and 6 basic group fragments has its statistical significance.
作者 齐磊 刘国庆
出处 《集宁师范学院学报》 2012年第4期105-110,共6页 Journal of Jining Normal University
关键词 转录假基因 碱基片段 相对频率 transcribed pseudogene basic group fragments relative frequency
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  • 1Luo LF, Ji FM. The preferential mode analysis of DNA sequence[J]. J Theor Biol, 1997,188:343-353.
  • 2Sharp PM, Li WH. The codon adaptation index -- a measure of directional synonymous codon usage bias, and its potential applications[J]. Nucleic Acids Resewch, 1987,15:1281-1295.
  • 3Luo LF, Li H. The statistical corelation of nuclcotidcs in protein-coding DNA sequences[J]. Bull Math Biol, 1991,53:345-353.
  • 4Nakamura Y, Tabata S. Codon-anticodon assignment and detection of codon usage trends in seven microbial gonomes[J].Microbiol Comp Genomics, 1997,2:299-312.
  • 5Pan A, Dutta C, Das J. Codon usage in highly expressed genes of Haemophillus influenzae and Mycobaterium tuberculosis: translational selection versus mutational bias[J]. Gene,1998,215:405--413.
  • 6Tiller ER, Collins RA. The contributions of replication orientation, gene direction~ and signal sequences to base-composition asymmetries in bacterial genomes[J]. J Mol Evol, 2000,50:249-257.
  • 7Cupta SIC., Ghosh TC. Gene expressivity is the main factor in dictating the codon usage variation among the genes in Pseudomonas aeruginosa[J]. Gene, 2001,273:63-70.
  • 8Li H, Luo LF. The relation between codon usage, base correlation and gene expression level in escherichia coil and yeast [J]. J Theor Biol, 1996,181:111-124.
  • 9Harrison P M, Gerstein M. Studying genomes through the aeons: protein families, pseudogenes and proteome evolution J Mol Biol, 2002, 318:1155-1174
  • 10Zhang Z L, Gerstein M. The human genome has 49 cytochrome c pseudogenes, including a relic of a primordial gene that still functions in mouse. Gene, 2003, 312:61-72

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