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A survey of trillions of base pairs of microbial DNA reveals a considerable degree of stop codon reassignment.
May 22, 2014|
RUTH WILLIAMSStop codons are not always genetic stop signs, according to a study published in Science today (May 22). A large proportion of bacteria and viruses have reassigned at least one stop codon—a signal marking the end of protein-coding sequences—to instead encode for an amino acid.
“This is the first real data point that looks at [stop codon reassignment] in an objective way to ask how common is it,” said Laura Landweber, a professor of ecology and evolutionary biology at Princeton University, who was not involved in the study.
Protein-coding DNA is written as a chain of trinucleotide words, or codons. There are 64 codons—the total possible combinations of the four DNA nucleotides, G, C, A, and T—and 61 of them encode amino acids. The remaining three—TGA, TAA, and TAG—are used at the end of protein-coding DNA sequences, and tell the cell’s translation machinery to stop adding amino acids.
This genetic code was believed to be universal to all life on the planet. That is, it was thought that TGA, TAA, and TAG meant “stop” no matter which organism they were in, just as a red octagonal road sign signals a driver to stop, no matter which country he’s in.
Over the past few decades, however, a handful of species have been discovered using stop codons to encode amino acids. To examine how often such codon reassignments occur in nature, Eddy Rubin, director of the US Department of Energy’s Joint Genome Institute in Walnut Creek, California, and his colleagues analyzed 5.6 trillion base pairs of microbial DNA sequence gathered from more than 250 different environments across the globe—including the sea, soil, and human stools.
Within the sequence data, which is stored in the Integrated Microbial Genome database, the team found evidence of stop codon reassignment in a “surprisingly significant fraction,” said Rubin. Indeed, “in some environments, close to 10 percent of the organisms use stop codons to code for amino acids,” he said.
The researchers observed reassignment of all three stop codons in some samples, but these changes varied in their frequency and distribution. In bacteria, for example, only reassignments of TGA were observed. While in eukaryotes, only TAA reassignments were observed. No stop codon reassignments were seen in archaea. And within viral sequences, the researchers found reassignments of both TGA and TAG.
The team also observed that viruses that infect bacteria—bacteriophages—sometimes had different codon reassignments to that of their hosts.
“[There was] the tacit expectation that parasites would match the genetic code usage of their host,” said Landweber. However, “at least with regard to stop codons, this shows that they don’t have to,” she said. In fact, added Rubin, there was evidence that one bacteriophage “uses the codon differences as a way to defeat its host.”
Beyond this case of a virus outsmarting its host, it is not clear what has led some organisms to recode their stop codons. One possibility, suggested Dieter Söll, a professor of molecular biophysics and biochemistry at Yale University, is that it may allow organisms to genetically encode proteins that contain unusual amino acids.
From when the genetic code was first deciphered until very recently, there was thought to be 20 amino acids commonly used to build proteins, said Söll. Within the last few decades, however, two additional genetically encoded amino acids have been discovered—selenocysteine and pyrrolysine—both of which are encoded by stop codons.
“My greatest excitement about this paper is really that we now know that there is a great frequency of stop codon changes,” Söll said. “I would imagine that if the biochemistry would be done on all these examples [of organisms that have reassigned stop codons],” he added, “one would very likely find additional genetically encoded non-standard amino acids.”
N.N. Ivanova et al., “Stop codon reassignments in the wild,” Science, 344: 909–13, 2014.
May 23, 2014
Does the reassigned stop coden always code for the same amino acid or does that differ?
May 23, 2014
If 1) ecological niche construction and 2) social niche construction associated with 3) nutrient stress and 4) social stress caused 5)the recoding to occur, the epigenetic landscape could be linked to the physical landscape of DNA in the organized genomes of species from microbes to man via 6) nutrient-dependent pheromone-controlled ecological adaptations manifested as 7) amino acid substitutions associated with the 8) morphological and behavioral phenotypes of 9) species diversification.
Cause and effect would then be linked from nutrient-dependent changes in the microRNA/messenger RNA balance to DNA methylation, intercellular signaling, and the de novo creation of novel cell types in the context of biophysical constraints associated with pheromone-controlled physiology of reproduction and cell-type differentiation in species from microbes to man. Wouldn't it?
Kudos to wctopp for asking if recoding always is for the same amino acid, which would not enable stress-related ecological adaptations. If recoding is for the same amino acid, you can forget my model of how ecological variation results in substitution of the amino acid glycine, which enables other amino acid substitutions to enable ecological adaptations. My model requires seemingly futile thermodynamic cycles of protein biosynthesis and degradation that facilitate nutrient-dependent amino acid substitutions that stabilize the genome as is required in the presence of changing ecology, in which atoms must be linked to ecosystems (and biodiversity via natural selection for food).