Evidence map›Paper›PMID 26392177›Full record

ArticleGenome biology2015

Comparative genomics of Steinernema reveals deeply conserved gene regulatory networks.

Adler R Dillman, Marissa Macchietto, Camille F Porter, Alicia Rogers, Brian Williams, Igor Antoshechkin, Ming-Min Lee, Zane Goodwin, Xiaojun Lu, Edwin E Lewis and 5 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
11.4field-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

48 citing papers in PubMed, 100 citations in OpenAlex.

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  13. An Intestinal Symbiotic Bacterial Strain ofInternational journal of molecular sciences · 2022
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  14. Review
  15. Article
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  17. Transcriptomic Analysis ofFrontiers in physiology · 2022
    Article
  18. Article
  19. Article
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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

15 authors at 8 institutions in 1 country.

Adler R DillmanDepartment of Nematology, University of California, Riverside, CA, 92521, USA. adler.dillman@ucr.edu.
Marissa MacchiettoDepartment of Developmental and Cell Biology, University of California, Irvine, CA, 92697, USA. mmacchie@uci.edu.
Camille F PorterDepartment of Biology and Evolutionary Ecology Laboratories, Brigham Young University, Provo, UT, 84602, USA. finli6@gmail.com.
Alicia RogersDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, 91125, USA. arogers@caltech.edu.
Brian WilliamsDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, 91125, USA. bawilli@caltech.edu.
Igor AntoshechkinDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, 91125, USA. igor.antoshechkin@caltech.edu.
Ming-Min LeeDepartment of Entomology, University of Arizona, Tucson, AZ, 85721, USA. mingmail@email.arizona.edu.
Zane GoodwinDivision of Biology and Biomedical Sciences, Washington University, St Louis, MO, 63110, USA. gzane01@gmail.com.
Xiaojun LuDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, 53706, USA. Luxiaojun@tsinghua.edu.cn.
Edwin E LewisDepartment of Entomology and Nematology, University of California, Davis, CA, 95616, USA. eelewis@ucdavis.edu.
Heidi Goodrich-BlairDepartment of Bacteriology, University of Wisconsin-Madison, Madison, WI, 53706, USA. hgblair@bact.wisc.edu.
S Patricia StockDepartment of Entomology, University of Arizona, Tucson, AZ, 85721, USA. spstock@email.arizona.edu.
Byron J AdamsDepartment of Biology and Evolutionary Ecology Laboratories, Brigham Young University, Provo, UT, 84602, USA. byron_adams@byu.edu.
Paul W SternbergDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, 91125, USA. pws@caltech.edu.
Ali MortazaviDepartment of Developmental and Cell Biology, University of California, Irvine, CA, 92697, USA. ali.mortazavi@uci.edu.
California Institute of Technology · USBrigham Young University · USUniversity of Arizona · USUniversity of California, Irvine · USUniversity of Wisconsin–Madison · USUniversity of California, Davis · USUniversity of California, Riverside · USWashington University in St. Louis · US

Funding

INSTITUTIONAL TRAINING GRANT IN GENOME SCIENCET32HG000044 · NHGRI · STANFORD UNIVERSITY · PI MICHAEL P. SNYDER · 1995 to 2026
$32.2M
PREDOCTORAL TRAINING IN BIOLOGY AND CHEMISTRYT32GM007616 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI STERNBERG, PAUL WARREN · 1985 to 2019
$22.9M
Comparative analysis of the 4D encoding of regulatory networks in stem cellsDP2GM111100 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI MORTAZAVI, SEYED ALI · 2013 to 2013
$2.3M
Howard Hughes Medical InstituteNCCDPHP CDC HHS DP2 GM111100NHGRI NIH HHS 5T32HG000044NHGRI NIH HHS T32 HG000044NIGMS NIH HHS 5T32GM007616NIGMS NIH HHS DP2 GM111100NIGMS NIH HHS T32 GM007616
6 · The paper itself

Abstract

backgroundParasitism is a major ecological niche for a variety of nematodes. Multiple nematode lineages have specialized as pathogens, including deadly parasites of insects that are used in biological control. We have sequenced and analyzed the draft genomes and transcriptomes of the entomopathogenic nematode Steinernema carpocapsae and four congeners (S. scapterisci, S. monticolum, S. feltiae, and S. glaseri).

resultsWe used these genomes to establish phylogenetic relationships, explore gene conservation across species, and identify genes uniquely expanded in insect parasites. Protein domain analysis in Steinernema revealed a striking expansion of numerous putative parasitism genes, including certain protease and protease inhibitor families, as well as fatty acid- and retinol-binding proteins. Stage-specific gene expression of some of these expanded families further supports the notion that they are involved in insect parasitism by Steinernema. We show that sets of novel conserved non-coding regulatory motifs are associated with orthologous genes in Steinernema and Caenorhabditis.

conclusionsWe have identified a set of expanded gene families that are likely to be involved in parasitism. We have also identified a set of non-coding motifs associated with groups of orthologous genes in Steinernema and Caenorhabditis involved in neurogenesis and embryonic development that are likely part of conserved protein-DNA relationships shared between these two genera.

Indexed as

PhylogenyAnimalsCaenorhabditisConserved SequenceGene Regulatory NetworksGenomePest Control, BiologicalProtein Structure, TertiaryRegulatory Sequences, Nucleic AcidRhabditidaSymbiosis

Identifiers

PMID26392177
PMCPMC4578762
OpenAlexW2101014533

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.