Evidence map›Paper›PMID 32066524›Full record

ArticleeLife2020

Synteny-based analyses indicate that sequence divergence is not the main source of orphan genes.

Nikolaos Vakirlis, Anne-Ruxandra Carvunis, Aoife McLysaght

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

90 citing papers in PubMed, 167 citations in OpenAlex.

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  17. Identification of a Highly VirulentPlants (Basel, Switzerland) · 2025
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  18. Unbiased anchors for reliable genome-wide synteny detection.Algorithms for molecular biology : AMB · 2025
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  19. Review
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30 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Nikolaos VakirlisSmurfit Institute of Genetics, Trinity College Dublin, University of Dublin, Dublin, Ireland.ORCID 0000-0001-7606-6987
Anne-Ruxandra CarvunisDepartment of Computational and Systems Biology, Pittsburgh Center for Evolutionary Biology and Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, United States.ORCID 0000-0002-6474-6413
Aoife McLysaghtSmurfit Institute of Genetics, Trinity College Dublin, University of Dublin, Dublin, Ireland.ORCID 0000-0003-2552-6220
Trinity College Dublin · IEUniversity of Pittsburgh · US

Funding

Deciphering the mechanisms and dynamics of proto-gene evolutionR00GM108865 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CARVUNIS, ANNE-RUXANDRA · 2017 to 2019
$747k
NIGMS NIH HHS R00 GM108865Seventh Framework Programme 309834Seventh Framework Programme 771419
6 · The paper itself

Abstract

The origin of 'orphan' genes, species-specific sequences that lack detectable homologues, has remained mysterious since the dawn of the genomic era. There are two dominant explanations for orphan genes: complete sequence divergence from ancestral genes, such that homologues are not readily detectable; and de novo emergence from ancestral non-genic sequences, such that homologues genuinely do not exist. The relative contribution of the two processes remains unknown. Here, we harness the special circumstance of conserved synteny to estimate the contribution of complete divergence to the pool of orphan genes. By separately comparing yeast, fly and human genes to related taxa using conservative criteria, we find that complete divergence accounts, on average, for at most a third of eukaryotic orphan and taxonomically restricted genes. We observe that complete divergence occurs at a stable rate within a phylum but at different rates between phyla, and is frequently associated with gene shortening akin to pseudogenization.

Indexed as

Evolution, MolecularAnimalsConserved SequenceDrosophila melanogasterGenesHumansPhylogenySaccharomyces cerevisiaeSequence HomologySyntenycomputational biologyconserved syntenyde novo gene emergenceD. melanogasterevolutionevolutionary biologygenetic noveltyhumanorphan genesS. cerevisiaesequence divergencesystems biology

Identifiers

PMID32066524
PMCPMC7028367
OpenAlexW3007397157

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.