Genome Research scroll

Home Help [Feedback] [For Subscribers] [Archive] [Search] --
 QUICK SEARCH:   [advanced]


     


Published online before print February 9, 2007
Genome Research, DOI: 10.1101/gr.5987307
OPEN ACCESS ARTICLE
This Article
OPEN ACCESS ARTICLE
Right arrow Full Text (PDF)
Right arrow Supplemental Research Data
Right arrow All Versions of this Article:
gr.5987307v1
17/4/405    most recent
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 Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Itzkovitz, S.
Right arrow Articles by Alon, U.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Itzkovitz, S.
Right arrow Articles by Alon, U.
Right arrowPubmed/NCBI databases
*Substance via MeSH
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Letter

The genetic code is nearly optimal for allowing additional information within protein-coding sequences

Shalev Itzkovitz1,2 and Uri Alon1,2,3

1 Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot 76100, Israel; 2 Department of Physics of Complex Systems, Weizmann Institute of Science, Rehovot 76100, Israel

DNA sequences that code for proteins need to convey, in addition to the protein-coding information, several different signals at the same time. These "parallel codes" include binding sequences for regulatory and structural proteins, signals for splicing, and RNA secondary structure. Here, we show that the universal genetic code can efficiently carry arbitrary parallel codes much better than the vast majority of other possible genetic codes. This property is related to the identity of the stop codons. We find that the ability to support parallel codes is strongly tied to another useful property of the genetic code—minimization of the effects of frame-shift translation errors. Whereas many of the known regulatory codes reside in nontranslated regions of the genome, the present findings suggest that protein-coding regions can readily carry abundant additional information.


3 Corresponding author.

E-mail uri.alon{at}weizmann.ac.il; fax 972-8-934125.

[Supplemental material is available online at www.genome.org.]

Article published online before print. Article and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.5987307


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


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
C. Zhang, W.-H. Li, A. R. Krainer, and M. Q. Zhang
RNA landscape of evolution for optimal exon and intron discrimination
PNAS, April 15, 2008; 105(15): 5797 - 5802.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
M. Pheasant and J. S. Mattick
Raising the estimate of functional human sequences
Genome Res., September 1, 2007; 17(9): 1245 - 1253.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] --
Genes Dev. Learn. Mem.
Protein Science RNA Genome Res.
Copyright © 2007 by Cold Spring Harbor Laboratory Press.