Evidence map›Paper›PMID 38659899›Full record

ArticlebioRxiv : the preprint server for biology2024

Order of amino acid recruitment into the genetic code resolved by Last Universal Common Ancestor's protein domains.

Sawsan Wehbi, Andrew Wheeler, Benoit Morel, Nandini Manepalli, Bui Quang Minh, Dante S Lauretta, Joanna Masel

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 3 countries.

Sawsan WehbiGenetics Graduate Interdisciplinary Program, University of Arizona, Tucson, Arizona, 85721, USA.ORCID 0000-0001-9498-9582
Andrew WheelerGenetics Graduate Interdisciplinary Program, University of Arizona, Tucson, Arizona, 85721, USA.ORCID 0000-0002-5347-5419
Benoit MorelComputational Molecular Evolution Group, Heidelberg Institute for Theoretical Studies, Heidelberg, Germany.ORCID 0000-0001-6286-4419
Nandini ManepalliDepartment of Molecular and Cellular Biology, University of Arizona, Tucson, AZ, 85721, USA.
Bui Quang MinhSchool of Computing, Australian National University, Canberra, ACT, Australia.ORCID 0000-0002-5535-6560
Dante S LaurettaLunar and Planetary Laboratory, University of Arizona, Tucson, AZ 85721, USA.ORCID 0000-0002-2597-5950
Joanna MaselDepartment of Ecology and Evolutionary Biology, University of Arizona, Tucson, AZ, 85721, USA.ORCID 0000-0002-7398-2127
University of Arizona · USAustralian National University · AUHeidelberg Institute for Theoretical Studies · DE

Funding

Computational and Mathematical Modeling of Biomedical SystemsT32GM132008 · NIGMS · UNIVERSITY OF ARIZONA · PI Ryan Gutenkunst, JOANNA MASEL · 2019 to 2026
$2.3M
NIGMS NIH HHS T32 GM132008
6 · The paper itself

Abstract

The current "consensus" order in which amino acids were added to the genetic code is based on potentially biased criteria, such as absence of sulfur-containing amino acids from the Urey-Miller experiment which lacked sulfur. More broadly, abiotic abundance might not reflect biotic abundance in the organisms in which the genetic code evolved. Here, we instead identify which protein domains date to the last universal common ancestor (LUCA), then infer the order of recruitment from deviations of their ancestrally reconstructed amino acid frequencies from the still-ancient post-LUCA controls. We find that smaller amino acids were added to the code earlier, with no additional predictive power in the previous "consensus" order. Metal-binding (cysteine and histidine) and sulfur-containing (cysteine and methionine) amino acids were added to the genetic code much earlier than previously thought. Methionine and histidine were added to the code earlier than expected from their molecular weights, and glutamine later. Early methionine availability is compatible with inferred early use of S-adenosylmethionine, and early histidine with its purine-like structure and the demand for metal-binding. Even more ancient protein sequences - those that had already diversified into multiple distinct copies prior to LUCA - have significantly higher frequencies of aromatic amino acids (tryptophan, tyrosine, phenylalanine and histidine), and lower frequencies of valine and glutamic acid than single copy LUCA sequences. If at least some of these sequences predate the current code, then their distinct enrichment patterns provide hints about earlier, alternative genetic codes.

Indexed as

antioxidantsastrobiologyBiological Sciencesearly lifeEvolutionmetalloproteinsOrigins of lifephylostratigraphy

Identifiers

PMID38659899
PMCPMC11042313
OpenAlexW4394890352

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.