Evidence map›Paper›PMID 29192334›Full record

ArticleJournal of molecular evolution2018

Putative Independent Evolutionary Reversals from Genotypic to Temperature-Dependent Sex Determination are Associated with Accelerated Evolution of Sex-Determining Genes in Turtles.

Robert Literman, Alexandria Burrett, Basanta Bista, Nicole Valenzuela

Abstract read
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In one paragraph

Article in Journal of molecular evolution, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 12% of its field
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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Temperature-Induced Sex Differentiation in River Prawn (International journal of molecular sciences · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. Thermosensitive sex chromosome dosage compensation in ZZ/ZW softshell turtles,Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Article
  8. A brief review of vertebrate sex evolution with a pledge for integrative research: towards 'Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. 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

4 authors at 1 institution in 1 country.

Robert LitermanDepartment of Ecology, Evolution and Organismal Biology, Iowa State University, Ames, IA, 50011, USA. literman@iastate.edu.ORCID 0000-0002-1784-0407
Alexandria BurrettDepartment of Ecology, Evolution and Organismal Biology, Iowa State University, Ames, IA, 50011, USA.
Basanta BistaDepartment of Ecology, Evolution and Organismal Biology, Iowa State University, Ames, IA, 50011, USA.
Nicole ValenzuelaDepartment of Ecology, Evolution and Organismal Biology, Iowa State University, Ames, IA, 50011, USA.
Iowa State University · US

Funding

Division of Environmental Biology 1310793Division of Integrative Organismal Systems 1555999Division of Molecular and Cellular Biosciences 1244355
6 · The paper itself

Abstract

The evolutionary lability of sex-determining mechanisms across the tree of life is well recognized, yet the extent of molecular changes that accompany these repeated transitions remain obscure. Most turtles retain the ancestral temperature-dependent sex determination (TSD) from which multiple transitions to genotypic sex determination (GSD) occurred independently, and two contrasting hypotheses posit the existence or absence of reversals back to TSD. Here we examined the molecular evolution of the coding regions of a set of gene regulators involved in gonadal development in turtles and several other vertebrates. We found slower molecular evolution in turtles and crocodilians compared to other vertebrates, but an acceleration in Trionychia turtles and at some phylogenetic branches demarcating major taxonomic diversification events. Of all gene classes examined, hormone signaling genes, and Srd5a1 in particular, evolve faster in many lineages and especially in turtles. Our data show that sex-linked genes do not follow a ubiquitous nor uniform pattern of molecular evolution. We then evaluated turtle nucleotide and protein evolution under two evolutionary hypotheses with or without GSD-to-TSD reversals, and found that when GSD-to-TSD reversals are considered, all transitional branches irrespective of direction, exhibit accelerated molecular evolution of nucleotide sequences, while GSD-to-TSD transitional branches also show acceleration in protein evolution. Significant changes in predicted secondary structure that may affect protein function were identified in three genes that exhibited hastened evolution in turtles compared to other vertebrates or in transitional versus non-transitional branches within turtles, rendering them candidates for a key role during SDM evolution in turtles.

Indexed as

AnimalsBase SequenceEvolution, MolecularFemaleGene Expression RegulationGenotypeMalePhylogenyReproductionSex ChromosomesSex Determination AnalysisSex Determination ProcessesTemperatureTurtlesGenotypic sex determinationSex determination mechanismsSubstitution rateTemperature-dependent sex determinationTurtles

Identifiers

PMID29192334
OpenAlexW2773011307

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.