Evidence map›Paper›PMID 31187122›Full record

ArticleMolecular biology and evolution2019

Rapid Evolution of Gained Essential Developmental Functions of a Young Gene via Interactions with Other Essential Genes.

Yuh Chwen G Lee, Iuri M Ventura, Gavin R Rice, Dong-Yuan Chen, Serafin U Colmenares, Manyuan Long

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Evolutionary innovation through fusion of sequences from across the tree of life.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  7. HP6/Umbrea is dispensable for viability and fertility, suggesting essentiality of newly evolved genes is rare.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

6 authors.

Yuh Chwen G LeeDepartment of Ecology and Evolution, The University of Chicago, Chicago, IL.
Iuri M VenturaDepartment of Ecology and Evolution, The University of Chicago, Chicago, IL.
Gavin R RiceDepartment of Evolution and Ecology, University of California, Davis, Davis, CA.
Dong-Yuan ChenDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA.
Serafin U ColmenaresDivision of Biological Systems and Engineering, Lawrence Berkeley National Laboratory, Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA.
Manyuan LongDepartment of Ecology and Evolution, The University of Chicago, Chicago, IL.

Funding

Reference-quality Drosophila genome assemblies for evolutionary analysis of previously inaccessible genomic regionsR01GM116113 · NIGMS · UNIVERSITY OF ARIZONA · PI CLARK, ANDREW G, LONG, MANYUAN · 2016 to 2019
$2.3M
The evolution of essential biological functions driven by new genes that reshapeF32GM109676 · NIGMS · UNIVERSITY OF CHICAGO · PI LEE, GRACE YUH CHWEN · 2014 to 2015
$106k
NIGMS NIH HHS F32 GM109676NIGMS NIH HHS R01 GM116113
6 · The paper itself

Abstract

New genes are of recent origin and only present in a subset of species in a phylogeny. Accumulated evidence suggests that new genes, like old genes that are conserved across species, can also take on important functions and be essential for the survival and reproductive success of organisms. Although there are detailed analyses of the mechanisms underlying new genes' gaining fertility functions, how new genes rapidly become essential for viability remains unclear. We focused on a young retro-duplicated gene (CG7804, which we named Cocoon) in Drosophila that originated between 4 and 10 Ma. We found that, unlike its evolutionarily conserved parental gene, Cocoon has evolved under positive selection and accumulated many amino acid differences at functional sites from the parental gene. Despite its young age, Cocoon is essential for the survival of Drosophila melanogaster at multiple developmental stages, including the critical embryonic stage, and its expression is essential in different tissues from those of its parental gene. Functional genomic analyses found that Cocoon acquired unique DNA-binding sites and has a contrasting effect on gene expression to that of its parental gene. Importantly, Cocoon binding predominantly locates at genes that have other essential functions and/or have multiple gene-gene interactions, suggesting that Cocoon acquired novel essential function to survival through forming interactions that have large impacts on the gene interaction network. Our study is an important step toward deciphering the evolutionary trajectory by which new genes functionally diverge from parental genes and become essential.

Indexed as

Evolution, MolecularGene DuplicationGenes, EssentialAmino Acid SubstitutionAnimalsDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsGene Expression Regulation, DevelopmentalGene Regulatory NetworksDNA-Binding ProteinsDrosophila ProteinsTBPH protein, DrosophiladevelopmentDrosophilagene networklethalityretrogene evolution

Identifiers

PMID31187122
PMCPMC6759199

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.