Evidence map›Paper›PMID 34242211›Full record

ArticlePLoS genetics2021

Genomic analyses of new genes and their phenotypic effects reveal rapid evolution of essential functions in Drosophila development.

Shengqian Xia, Nicholas W VanKuren, Chunyan Chen, Li Zhang, Clause Kemkemer, Yi Shao, Hangxing Jia, UnJin Lee, Alexander S Advani, Andrea Gschwend and 4 more

Abstract read
In one paragraph

Article in PLoS genetics, 2021. 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. Article
  2. De Novo Genes: Current Status and Future Goals.Genome biology and evolution · 2025
    Article
  3. Gene age shapes functional and evolutionary properties of theProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. De Novo Genes.Annual review of genetics · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. 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
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Nonadaptive molecular evolution of seminal fluid proteins in Drosophila.Evolution; international journal of organic evolution · 2021
    Article
  20. 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

14 authors.

Shengqian XiaDepartment of Ecology and Evolution, The University of Chicago, Chicago, Illinois, United States of America.ORCID 0000-0002-9264-3649
Nicholas W VanKurenDepartment of Ecology and Evolution, The University of Chicago, Chicago, Illinois, United States of America.ORCID 0000-0001-8633-8851
Chunyan ChenState Key Laboratory of Integrated Management of Pest Insects and Rodents & Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Li ZhangDepartment of Ecology and Evolution, The University of Chicago, Chicago, Illinois, United States of America.ORCID 0000-0002-0698-0754
Clause KemkemerDepartment of Ecology and Evolution, The University of Chicago, Chicago, Illinois, United States of America.
Yi ShaoState Key Laboratory of Integrated Management of Pest Insects and Rodents & Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Hangxing JiaState Key Laboratory of Integrated Management of Pest Insects and Rodents & Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
UnJin LeeDepartment of Ecology and Evolution, The University of Chicago, Chicago, Illinois, United States of America.
Alexander S AdvaniDepartment of Ecology and Evolution, The University of Chicago, Chicago, Illinois, United States of America.ORCID 0000-0003-0364-0321
Andrea GschwendDepartment of Horticulture & Crop Science, The Ohio State University, Columbus, Ohio, United States of America.ORCID 0000-0002-6208-2457
Maria D VibranovskiDepartment of Genetics and Evolutionary Biology, University of São Paulo, São Paulo, Brazil.ORCID 0000-0001-8313-9726
Sidi ChenDepartment of Genetics, Yale School of Medicine, West Haven, Connecticut, United States of America.
Yong E ZhangState Key Laboratory of Integrated Management of Pest Insects and Rodents & Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.ORCID 0000-0003-3770-2383
Manyuan LongDepartment of Ecology and Evolution, The University of Chicago, Chicago, Illinois, United States of America.ORCID 0000-0002-6755-197X

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
NIGMS NIH HHS R01 GM116113
6 · The paper itself

Abstract

It is a conventionally held dogma that the genetic basis underlying development is conserved in a long evolutionary time scale. Ample experiments based on mutational, biochemical, functional, and complementary knockdown/knockout approaches have revealed the unexpectedly important role of recently evolved new genes in the development of Drosophila. The recent progress in the genome-wide experimental testing of gene effects and improvements in the computational identification of new genes (< 40 million years ago, Mya) open the door to investigate the evolution of gene essentiality with a phylogenetically high resolution. These advancements also raised interesting issues in techniques and concepts related to phenotypic effect analyses of genes, particularly of those that recently originated. Here we reported our analyses of these issues, including reproducibility and efficiency of knockdown experiment and difference between RNAi libraries in the knockdown efficiency and testing of phenotypic effects. We further analyzed a large data from knockdowns of 11,354 genes (~75% of the Drosophila melanogaster total genes), including 702 new genes (~66% of the species total new genes that aged < 40 Mya), revealing a similarly high proportion (~32.2%) of essential genes that originated in various Sophophora subgenus lineages and distant ancestors beyond the Drosophila genus. The transcriptional compensation effect from CRISPR knockout were detected for highly similar duplicate copies. Knockout of a few young genes detected analogous essentiality in various functions in development. Taken together, our experimental and computational analyses provide valuable data for detection of phenotypic effects of genes in general and further strong evidence for the concept that new genes in Drosophila quickly evolved essential functions in viability during development.

Indexed as

Evolution, MolecularAnimalsBiological EvolutionDrosophila melanogasterDrosophila ProteinsGene DuplicationGene Knockdown TechniquesGenes, EssentialGenomicsGenotypeModels, GeneticMutationPhenotypePhylogenyReproducibility of ResultsDrosophila Proteins

Identifiers

PMID34242211
PMCPMC8270118

What OpenQuestion holds

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LicenceCC BY
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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.