Evidence map›Paper›PMID 11087835›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Testing a biosynthetic theory of the genetic code: fact or artifact?

T A Ronneberg, L F Landweber, S J Freeland

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

  1. Fitting the standard genetic code into its triplet table.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  2. Evolution of the Standard Genetic Code.Journal of molecular evolution · 2021
    Article
  3. Optimal Evolution of the Standard Genetic Code.Journal of molecular evolution · 2021
    Article
  4. Genetic code and metabolism: The perpetual waltz.The Journal of biological chemistry · 2018
    Article
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  6. Review
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  10. Article
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  12. Imprints of the genetic code in the ribosome.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. A content-centric organization of the genetic code.Genomics, proteomics & bioinformatics · 2007
    Article
  18. Article
  19. On the structural regularity in nucleobases and amino acids and relationship to the origin and evolution of the genetic code.Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life · 2005
    Article
  20. A new classification scheme of the genetic code.Journal of molecular evolution · 2004
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

T A RonnebergDepartments of Ecology and Evolutionary Biology, and Chemistry, Princeton University, Princeton, NJ 08544, USA.
L F Landweber
S J Freeland

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has long been conjectured that the canonical genetic code evolved from a simpler primordial form that encoded fewer amino acids [e.g., Crick, F. H. C. (1968) J. Mol. Biol. 38, 367-379]. The most influential form of this idea, "code coevolution" [Wong, J. T.-F. (1975) Proc. Natl. Acad. Sci. USA 72, 1909-1912], proposes that the genetic code coevolved with the invention of biosynthetic pathways for new amino acids. It further proposes that a comparison of modern codon assignments with the conserved metabolic pathways of amino acid biosynthesis can inform us about this history of code expansion. Here we re-examine the biochemical basis of this theory to test the validity of its statistical support. We show that the theory's definition of "precursor-product" amino acid pairs is unjustified biochemically because it requires the energetically unfavorable reversal of steps in extant metabolic pathways to achieve desired relationships. In addition, the theory neglects important biochemical constraints when calculating the probability that chance could assign precursor-product amino acids to contiguous codons. A conservative correction for these errors reveals a surprisingly high 23% probability that apparent patterns within the code are caused purely by chance. Finally, even this figure rests on post hoc assumptions about primordial codon assignments, without which the probability rises to 62% that chance alone could explain the precursor-product pairings found within the code. Thus we conclude that coevolution theory cannot adequately explain the structure of the genetic code.

Indexed as

Genetic CodeCodonEvolution, MolecularModels, GeneticCodon

Identifiers

PMID11087835
PMCPMC17637

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.