Skip Navigation


Bioinformatics Advance Access originally published online on January 22, 2004
This Article
Right arrow FREE Full Text (Print PDF) Freely available
Right arrow FREE Full Text (Screen PDF)
Right arrow All Versions of this Article:
20/4/445    most recent
btg443v1
Right arrow Comments: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Comments are posted
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 ISI Web of Science
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 arrow Search for citing articles in:
ISI Web of Science (10)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Kochetov, A. V.
Right arrow Articles by Sarai, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kochetov, A. V.
Right arrow Articles by Sarai, A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Bioinformatics 20(4) © Oxford University Press 2004; all rights reserved.

Discovery Note

Translational polymorphism as a potential source of plant proteins variety in Arabidopsis thaliana

Alex V. Kochetov 1,* and Akinori Sarai 2,3

1 Institute of Cytology and Genetics, Pr. Lavrentieva 10, Novosibirsk 630090, Russia and 2 Tsukuba Institute, The Institute of Physical and Chemical Research (RIKEN), Tsukuba, Japan

Received on August 22, 2003 ; accepted on September 9, 2003
Advance Access Publication January 22, 2004

Motivation: According to scanning model, 40S ribosomal subunits can either initiate translation at start AUG codon in suboptimal context or miss it and initiate translation at downstream AUG(s), thereby producing several proteins. Functional significance of such a protein translational polymorphism is still unknown.

Results: We compared predicted subcellular localizations of annotated Arabidopsis thaliana proteins and their potential N-terminally truncated forms started from the nearest downstream in-frame AUG codons. It was found that localizations of full and N-truncated proteins differ in many cases: 12.2% of N-truncated proteins acquired sorting signals de novo and 5.7% changed their predicted subcellular locations (mitochodria, chloroplast or secretory pathway). It is likely that the in-frame downstream AUGs may be frequently utilized to synthesize proteins possessing new functional properties and such a translational polymorphism may serve as an important source of cellular and organelle proteomes.

Availability: Detailed description of arabidopsis mRNAs potentially producing novel functional protein forms is available by request.

Contact: Alex Kochetov, ak{at}bionet.nsc.ru

* To whom correspondence should be addressed.

3 Present address: Kyushu Institute of Technology, Department of Biochemical Engineering and Science, Iizuka 820-8502, Japan.


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
J. Cai, J. Zhang, Y. Huang, and Y. Li
ATID: a web-oriented database for collection of publicly available alternative translational initiation events
Bioinformatics, December 1, 2005; 21(23): 4312 - 4314.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
A. V. Kochetov
AUG codons at the beginning of protein coding sequences are frequent in eukaryotic mRNAs with a suboptimal start codon context
Bioinformatics, April 1, 2005; 21(7): 837 - 840.
[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.