REHOVOT, Israel (Fri., Feb. 9, 2007) -- Today, researchers from The Weizmann Institute of Science report the discovery of two new properties of the genetic code. Their work, which appears online in Genome Research, shows that the genetic code—used by organisms as diverse as reef coral, termites, and humans—is nearly optimal for encoding signals of any length in parallel to sequences that code for proteins. In addition, they report that the genetic code is organized so efficiently that when the cellular machinery misses a beat during protein synthesis, the process is promptly halted before energy and resources are wasted.
"Our findings open the possibility that genes can carry additional, currently unknown codes," explains Dr. Uri Alon, principal investigator on the project. "These findings point at possible selection forces that may have shaped the universal genetic code."
The genetic code consists of 61 codons—tri-nucleotide sequences of DNA—that encode 20 amino acids, the building blocks of proteins. In addition, three codons signal the cellular machinery to stop protein synthesis after a full-length protein is built.
While the best-known function of genes is to code for proteins, the DNA sequences of genes also harbor signals for folding, organization, regulation, and splicing. These DNA sequences are typically a bit longer: from four to 150 or more nucleotides in length.
Alon and his doctoral student Shalev Itzkovitz compared the real genetic code to alternative, hypothetical genetic codes with equivalent codon-amino acid assignment characteristics. Remarkably, Itzkovitz and Alon showed that the real genetic code was superior to the vast majority of alternative genetic codes in terms of its ability to encode other information in protein-coding genes—such as splice sites, mRNA secondary structure, or regulatory signals.
Itzkovitz and Alon also demonstrated that the real genetic code provides for the quickest incorporation of a stop signal—compared to most of the alternative genetic codes—in cases where protein synthesis has gone amiss (situations that scientists call "frameshift errors"). This helps the cell to conserve its energy and resources.
"We think that the ability to carry parallel codes—or information beyond the amino acid code—may be a side effect of selection for avoiding aberrant protein synthesis," says Itzkovitz. "These parallel codes were probably exploited during evolution to allow genes to support a wide range of signals to regulate and modify biological processes in cells."
The results of this study will be useful for researchers seeking to identify DNA sequences that regulate the expression and function of the genome. Many currently known regulatory sequences reside in non-protein-coding regions, but this may give scientists incentive to delve deeper into the protein-coding genes in order to solve life's mysteries.
About Genome Research: Genome Research (www.genome.org) is an international, continuously published, peer-reviewed journal published by Cold Spring Harbor Laboratory Press. Launched in 1995, it is one of the five most highly cited primary research journals in genetics and genomics.
About Cold Spring Harbor Laboratory Press: Cold Spring Harbor Laboratory Press is an internationally renowned publisher of books, journals, and electronic media, located on Long Island, New York. It is a division of Cold Spring Harbor Laboratory, an innovator in life science research and the education of scientists, students, and the public. For more information, visit www.cshlpress.com.
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