Evidence map›Paper›PMID 24763277›Full record

ArticlePLoS genetics2014

A novel highly divergent protein family identified from a viviparous insect by RNA-seq analysis: a potential target for tsetse fly-specific abortifacients.

Joshua B Benoit, Geoffrey M Attardo, Veronika Michalkova, Tyler B Krause, Jana Bohova, Qirui Zhang, Aaron A Baumann, Paul O Mireji, Peter Takáč, David L Denlinger and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. 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. Article
  18. Article
  19. 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

12 authors at 6 institutions in 3 countries.

Joshua B BenoitDivision of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.
Geoffrey M AttardoDivision of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.
Veronika MichalkovaDivision of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America; Section of Molecular and Applied Zoology, Institute of Zoology, Slovak Academy of Sciences, Bratislava, Slovakia.
Tyler B KrauseDivision of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.
Jana BohovaSection of Molecular and Applied Zoology, Institute of Zoology, Slovak Academy of Sciences, Bratislava, Slovakia.
Qirui ZhangDepartments of Entomology and Evolution, Ecology and Organismal Biology, The Ohio State University, Columbus, Ohio, United States of America.
Aaron A BaumannJanelia Farm Research Campus, Howard Hughes Medical Institute, Ashburn, Virginia, United States of America.
Paul O MirejiDepartment of Biochemistry and Molecular Biology, Egerton University, Njoro, Kenya.
Peter TakáčSection of Molecular and Applied Zoology, Institute of Zoology, Slovak Academy of Sciences, Bratislava, Slovakia.
David L DenlingerDepartments of Entomology and Evolution, Ecology and Organismal Biology, The Ohio State University, Columbus, Ohio, United States of America.
Jose M RibeiroLaboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, United States of America.
Serap AksoyDivision of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, United States of America.
Yale University · USInstitute of Zoology of the Slovak Academy of Sciences · SKThe Ohio State University · USEgerton University · KEHoward Hughes Medical Institute · USNational Institute of Allergy and Infectious Diseases · US

Funding

Vector-Borne Diseases: Biology Of Vector Host RelationshipZIAAI000810 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI RIBEIRO, JOSE · 2009 to 2025
$20.8M
Tsetse Fecundity Reduction for Trypanosomiasis ControlR01AI081774 · NIAID · YALE UNIVERSITY · PI AKSOY, SERAP · 2009 to 2013
$2.0M
Tsetse Transmitted African TrypanosomiasisD43TW007391 · FIC · YALE UNIVERSITY · PI AKSOY, SERAP · 2008 to 2017
$1.8M
Expanding the toolbox for tsetse reproductive biologyR21AI109263 · NIAID · YALE UNIVERSITY · PI AKSOY, SERAP, ATTARDO, GEOFFREY M · 2014 to 2015
$428k
Molecular regulation of diapause in Culex pipiensR56AI058279 · NIAID · OHIO STATE UNIVERSITY · PI DENLINGER, DAVID L · 2012 to 2012
$273k
Lipid metabolism during tsetse reproductionF32AI093023 · NIAID · YALE UNIVERSITY · PI BENOIT, JOSH B. · 2011 to 2013
$114k
FIC NIH HHS D43 TW007391NIAID NIH HHS 2R56 AI058279NIAID NIH HHS AI081774NIAID NIH HHS F32 AI093023NIAID NIH HHS F32AI093023NIAID NIH HHS R01 AI081774NIAID NIH HHS R21 AI109263NIAID NIH HHS R56 AI058279
6 · The paper itself

Abstract

In tsetse flies, nutrients for intrauterine larval development are synthesized by the modified accessory gland (milk gland) and provided in mother's milk during lactation. Interference with at least two milk proteins has been shown to extend larval development and reduce fecundity. The goal of this study was to perform a comprehensive characterization of tsetse milk proteins using lactation-specific transcriptome/milk proteome analyses and to define functional role(s) for the milk proteins during lactation. Differential analysis of RNA-seq data from lactating and dry (non-lactating) females revealed enrichment of transcripts coding for protein synthesis machinery, lipid metabolism and secretory proteins during lactation. Among the genes induced during lactation were those encoding the previously identified milk proteins (milk gland proteins 1-3, transferrin and acid sphingomyelinase 1) and seven new genes (mgp4-10). The genes encoding mgp2-10 are organized on a 40 kb syntenic block in the tsetse genome, have similar exon-intron arrangements, and share regions of amino acid sequence similarity. Expression of mgp2-10 is female-specific and high during milk secretion. While knockdown of a single mgp failed to reduce fecundity, simultaneous knockdown of multiple variants reduced milk protein levels and lowered fecundity. The genomic localization, gene structure similarities, and functional redundancy of MGP2-10 suggest that they constitute a novel highly divergent protein family. Our data indicates that MGP2-10 function both as the primary amino acid resource for the developing larva and in the maintenance of milk homeostasis, similar to the function of the mammalian casein family of milk proteins. This study underscores the dynamic nature of the lactation cycle and identifies a novel family of lactation-specific proteins, unique to Glossina sp., that are essential to larval development. The specificity of MGP2-10 to tsetse and their critical role during lactation suggests that these proteins may be an excellent target for tsetse-specific population control approaches.

Indexed as

Abortifacient AgentsAmino Acid SequenceAnimalsExonsFemaleFertilityGene Expression ProfilingGene Knockdown TechniquesGenes, InsectInsect ProteinsIntronsLactationLipid MetabolismMaleMilk ProteinsPhylogenyAbortifacient AgentsInsect ProteinsMilk ProteinsProteomeRNA

Identifiers

PMID24763277
PMCPMC3998918
OpenAlexW2113926825

What OpenQuestion holds

Textmetadata
LicenceCC0
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.