Genome annotation improvements from cross-phyla proteogenomics and time-of-day differences in malaria mosquito proteins using untargeted quantitative proteomics.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 24 10 2018
accepted: 11 07 2019
entrez: 30 7 2019
pubmed: 30 7 2019
medline: 5 3 2020
Statut: epublish

Résumé

The malaria mosquito, Anopheles stephensi, and other mosquitoes modulate their biology to match the time-of-day. In the present work, we used a non-hypothesis driven approach (untargeted proteomics) to identify proteins in mosquito tissue, and then quantified the relative abundance of the identified proteins from An. stephensi bodies. Using these quantified protein levels, we then analyzed the data for proteins that were only detectable at certain times-of-the day, highlighting the need to consider time-of-day in experimental design. Further, we extended our time-of-day analysis to look for proteins which cycle in a rhythmic 24-hour ("circadian") manner, identifying 31 rhythmic proteins. Finally, to maximize the utility of our data, we performed a proteogenomic analysis to improve the genome annotation of An. stephensi. We compare peptides that were detected using mass spectrometry but are 'missing' from the An. stephensi predicted proteome, to reference proteomes from 38 other primarily human disease vector species. We found 239 such peptide matches and reveal that genome annotation can be improved using proteogenomic analysis from taxonomically diverse reference proteomes. Examination of 'missing' peptides revealed reading frame errors, errors in gene-calling, overlapping gene models, and suspected gaps in the genome assembly.

Identifiants

pubmed: 31356616
doi: 10.1371/journal.pone.0220225
pii: PONE-D-18-29260
pmc: PMC6663012
doi:

Substances chimiques

Insect Proteins 0
Peptides 0

Banques de données

Dryad
['10.5061/dryad.8p20m31']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0220225

Subventions

Organisme : Wellcome Trust
ID : 202769/Z/16/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 095831/Z/11/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 095831
Pays : United Kingdom

Déclaration de conflit d'intérêts

TLB has received salary from Rapid Novor. TLB’s employment at Rapid Novor does not alter our adherence to PLOS ONE policies on sharing data and materials. The other authors have declared that no competing interests exist. The specific roles of all authors are articulated in the ‘author contributions’ section.

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Auteurs

Lisa Imrie (L)

SynthSys-Synthetic and Systems Biology, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom.

Thierry Le Bihan (T)

SynthSys-Synthetic and Systems Biology, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Centre for Immunity, Infection and Evolution, University of Edinburgh, Edinburgh, United Kingdom.
Rapid Novor, Kitchener, Ontario, Canada.

Áine O'Toole (Á)

Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, United Kingdom.

Paul V Hickner (PV)

Eck Institute for Global Health, University of Notre Dame, Notre Dame, Indiana, United States of America.

W Augustine Dunn (WA)

Boston Children's Hospital, Boston, Massachusetts, United States of America.

Benjamin Weise (B)

Centre for Immunity, Infection and Evolution, University of Edinburgh, Edinburgh, United Kingdom.

Samuel S C Rund (SSC)

Centre for Immunity, Infection and Evolution, University of Edinburgh, Edinburgh, United Kingdom.
Eck Institute for Global Health, University of Notre Dame, Notre Dame, Indiana, United States of America.

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Classifications MeSH