Evidence map›Paper›PMID 26680200›Full record

ArticleScience (New York, N.Y.)2015

An essential cell cycle regulation gene causes hybrid inviability in Drosophila.

Nitin Phadnis, EmilyClare P Baker, Jacob C Cooper, Kimberly A Frizzell, Emily Hsieh, Aida Flor A de la Cruz, Jay Shendure, Jacob O Kitzman, Harmit S Malik

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Article
  2. Article
  3. A newborn F-box gene blocks gene flow by selectively degrading phosphoglucomutase in species hybrids.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Do genetic loci that cause reproductive isolation in the lab inhibit gene flow in nature?Evolution; international journal of organic evolution · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Comparative studies on speciation: 30 years since Coyne and Orr.Evolution; international journal of organic evolution · 2021
    Article
  18. Review
  19. Review
  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

9 authors.

Nitin PhadnisDepartment of Biology, University of Utah, Salt Lake City, UT 84112, USA. nitin.phadnis@utah.edu hsmalik@fhcrc.org.
EmilyClare P BakerBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Jacob C CooperDepartment of Biology, University of Utah, Salt Lake City, UT 84112, USA.
Kimberly A FrizzellDepartment of Biology, University of Utah, Salt Lake City, UT 84112, USA.
Emily HsiehBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Aida Flor A de la CruzBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Jay ShendureGenome Sciences, University of Washington, Seattle, WA 98195, USA. Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA.
Jacob O KitzmanGenome Sciences, University of Washington, Seattle, WA 98195, USA. Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA.
Harmit S MalikBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. Howard Hughes Medical Institute, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. nitin.phadnis@utah.edu hsmalik@fhcrc.org.

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Genetic Conflict Shapes Centromeres and HeterochromatinR01GM074108 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MALIK, HARMIT S. · 2005 to 2022
$6.1M
Massively Parallel Contiguity MappingR01HG006283 · NHGRI · UNIVERSITY OF WASHINGTON · PI SHENDURE, JAY ASHOK · 2011 to 2016
$3.4M
The molecular basis of speciation in DrosophilaR01GM115914 · NIGMS · UNIVERSITY OF UTAH · PI PHADNIS, NITIN · 2015 to 2019
$1.5M
FHCRC High-Performance Computing ClusterS10OD020069 · OD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KOOPERBERG, CHARLES L · 2015 to 2015
$600k
Howard Hughes Medical InstituteNCI NIH HHS P30 CA015704NHGRI NIH HHS HG006283NHGRI NIH HHS R01 HG006283NICHD NIH HHS 5T32 HD0741NIGMS NIH HHS R01 GM074108NIGMS NIH HHS R01 GM115914NIH HHS S10 OD020069
6 · The paper itself

Abstract

Speciation, the process by which new biological species arise, involves the evolution of reproductive barriers, such as hybrid sterility or inviability between populations. However, identifying hybrid incompatibility genes remains a key obstacle in understanding the molecular basis of reproductive isolation. We devised a genomic screen, which identified a cell cycle-regulation gene as the cause of male inviability in hybrids resulting from a cross between Drosophila melanogaster and D. simulans. Ablation of the D. simulans allele of this gene is sufficient to rescue the adult viability of hybrid males. This dominantly acting cell cycle regulator causes mitotic arrest and, thereby, inviability of male hybrid larvae. Our genomic method provides a facile means to accelerate the identification of hybrid incompatibility genes in other model and nonmodel systems.

Indexed as

Genetic SpeciationReproductive IsolationAllelesAnimalsCarrier ProteinsCell CycleChimeraCrosses, GeneticDrosophila melanogasterDrosophila simulansGene Expression Regulation, DevelopmentalGenes, EssentialGenes, InsectGenes, LethalMaleMolecular Sequence DataCarrier ProteinsGFZF protein, Drosophila

Identifiers

PMID26680200
PMCPMC4703311

What OpenQuestion holds

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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.