Skip Navigation



MBE Advance Access published online on July 28, 2003

Molecular Biology and Evolution, doi:10.1093/molbev/msg203
Molecular Biology and Evolution © Society for Molecular Biology and Evolution 2003; all rights reserved
This Article
Right arrow Advance Access manuscript (PDF) Freely available
Right arrow All Versions of this Article:
20/12/1978    most recent
msg203v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Zhuang, Y.
Right arrow Articles by Li, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zhuang, Y.
Right arrow Articles by Li, Y.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Accepted June 18, 2003
© 2003 Society for Molecular Biology and Evolution

Original Articles

Comparative Analysis of Amino Acid Usage and Protein Length Distribution between Alternatively and Non-Alternatively Spliced Genes across Six Eukaryotic Genomes

Yonglong Zhuang 1, Fei Ma 1*, Jesse Li-Ling 2, Xiaofeng Xu 3, and Yanda Li 1

1 Institute of Bioinformatics, Tsinghua University, Beijing, 100084 China
2 Department of Medical Genetics, China Medical University, Shenyang, 110001 China
3 Life Science College, Nanjing Normal University, Nanjing, 210097 China

* To whom correspondence should be addressed. E-mail: bphma{at}mail.tsinghua.edu.cn.


   Abstract

Alternative splicing has been discovered in nearly all metazoan organisms as a mechanism to increase the diversity of gene products. However, the origin and evolution of alternatively spliced genes are yet poorly understood. To understand the mechanisms for the evolution of alternatively spliced genes, it may be important to study the differences between alternatively and non-alternatively spliced genes. The aim of this research was to compare amino acid usage and protein length distribution between alternatively and non-alternatively spliced genes across six nearly complete eukaryotic genomes including those of human (Homo sapiens), mouse (Mus musculus), rat (Rattus norvegicus), fruit fly (Drosophila melanogaster), C. elegans, and bovine (Bos taurus). Our results have suggested that (1) Across the six species, alternatively and non-alternatively spliced genes have very similar tendency for amino acids usage for not only the overall scale but also those highly expressed genes, with all of the highly expressed genes having preferred amino acids including A, E, G, K, L, P, S, V, R, T and D. (2) For not only the overall genes but also those highly expressed ones, the average length of the protein products of alternatively spliced genes is significantly greater than that of non-alternatively spliced ones. On the other hand, distributions of protein lengths for the two groups of genes are very similar among all six species. Based on above results, we propose that alternatively spliced genes may have originated from non-alternatively spliced ones through events such as DNA mutations or gene fusion.

Key Words: amino acid usage, alternatively spliced genes, protein length distribution, eukaryotes, evolution


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
BioinformaticsHome page
Y. Lian and H. R. Garner
Evidence for the regulation of alternative splicing via complementary DNA sequence repeats
Bioinformatics, April 15, 2005; 21(8): 1358 - 1364.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.