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首页|期刊导航|安徽农业大学学报|人类1号染色体可变剪接与普通剪接基因同义密码子的使用分析I.同义密码子偏爱使用分析

人类1号染色体可变剪接与普通剪接基因同义密码子的使用分析I.同义密码子偏爱使用分析

陈学平 武耀廷 郭家明 张成 马飞

安徽农业大学学报2004,Vol.31Issue(1):1-5,5.
安徽农业大学学报2004,Vol.31Issue(1):1-5,5.

人类1号染色体可变剪接与普通剪接基因同义密码子的使用分析I.同义密码子偏爱使用分析

Synonymous Codon Usage of Both Alternatively and Commonly Spliced Genes in Human Chromosome 1 I:Synonymous Codon Usage Bias Analysis

陈学平 1武耀廷 2郭家明 1张成 3马飞4

作者信息

  • 1. 中国科学技术大学经济技术学院,合肥,230052
  • 2. 中国热带农业科学院热带作物生物技术国家重点实验室,海口,571101
  • 3. 合肥市植保站,合肥,230031
  • 4. 厦门大学生命科学学院,厦门,361005
  • 折叠

摘要

Abstract

It is already clear that alternative splicing has an extremely important role in expanding the protein diversity. Comparative study of the codon usage patterns of alternatively and commonly spliced genes may thereby be necessary. In this paper, the patterns of codon usage bias of two kinds of human genes, alternatively spliced genes and commonly spliced genes, were formulated through analyzing 344 non-redundant protein coding sequences from alternatively spliced genes (188183 codons) and 386 from commonly spliced genes (223116 codons) in human chromosome 1. Overall codon usage data analysis indicated that the alternatively spliced genes showed a stronger codon usage bias than commonly spliced genes. Very extensive heterogeneity of G+C content in silent third codon position (GC3s) was evident among these genes, and GC3s content of alternatively spliced genes was higher than that of commonly spliced genes. G- or C-ending codons were more abundant in alternatively spliced genes than commonly spliced genes in human chromosome 1. The causation of differences created could be explained by pre-mRNA structural characteristics of alternatively spliced genes influencing their codon usage bias.

关键词

可变剪接/普通剪接/密码子使用/人类

Key words

alternative splicing/common splicing/codon usage/human

分类

生物科学

引用本文复制引用

陈学平,武耀廷,郭家明,张成,马飞..人类1号染色体可变剪接与普通剪接基因同义密码子的使用分析I.同义密码子偏爱使用分析[J].安徽农业大学学报,2004,31(1):1-5,5.

基金项目

China postdoctoral programs foundation(200211). (200211)

安徽农业大学学报

OA北大核心CSCDCSTPCD

1672-352X

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