Evidence map›Paper›PMID 33076839›Full record

ArticleBMC genomics2020

Temporal proteomic profiling reveals insight into critical developmental processes and temperature-influenced physiological response differences in a bivalve mollusc.

Shelly A Wanamaker, Kaitlyn R Mitchell, Rhonda Elliott Thompson, Benoit Eudeline, Brent Vadopalas, Emma B Timmins-Schiffman, Steven B Roberts

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Shelly A WanamakerSchool of Aquatic and Fishery Sciences, University of Washington, Seattle, Washington, 98105, USA. strigg@uw.edu.ORCID http://orcid.org/0000-0001-6904-4149
Kaitlyn R MitchellSchool of Aquatic and Fishery Sciences, University of Washington, Seattle, Washington, 98105, USA.
Rhonda Elliott ThompsonSchool of Aquatic and Fishery Sciences, University of Washington, Seattle, Washington, 98105, USA.
Benoit EudelineTaylor Shellfish Hatchery, Quilcene, Washington, USA.
Brent VadopalasWashington Sea Grant, University of Washington, Seattle, Washington, USA.
Emma B Timmins-SchiffmanDepartment of Genome Sciences, University of Washington, Seattle, Washington, USA.
Steven B RobertsSchool of Aquatic and Fishery Sciences, University of Washington, Seattle, Washington, 98105, USA.
University of Washington · USTaylor Shellfish Farms (United States) · US

Funding

MOLECULAR BASIS OF DARIERS DISEASER01AR041700 · NIAMS · UNIVERSITY OF ROCHESTER · PI EPSTEIN, ERVIN H · 1992 to 1998
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Washington Sea Grant, University of Washington NA140AR4170078
6 · The paper itself

Abstract

backgroundProtein expression patterns underlie physiological processes and phenotypic differences including those occurring during early development. The Pacific oyster (Crassostrea gigas) undergoes a major phenotypic change in early development from free-swimming larval form to sessile benthic dweller while proliferating in environments with broad temperature ranges. Despite the economic and ecological importance of the species, physiological processes occurring throughout metamorphosis and the impact of temperature on these processes have not yet been mapped out.

resultsTowards this, we comprehensively characterized protein abundance patterns for 7978 proteins throughout metamorphosis in the Pacific oyster at different temperature regimes. We used a multi-statistical approach including principal component analysis, ANOVA-simultaneous component analysis, and hierarchical clustering coupled with functional enrichment analysis to characterize these data. We identified distinct sets of proteins with time-dependent abundances generally not affected by temperature. Over 12 days, adhesion and calcification related proteins acutely decreased, organogenesis and extracellular matrix related proteins gradually decreased, proteins related to signaling showed sinusoidal abundance patterns, and proteins related to metabolic and growth processes gradually increased. Contrastingly, different sets of proteins showed temperature-dependent abundance patterns with proteins related to immune response showing lower abundance and catabolic pro-growth processes showing higher abundance in animals reared at 29 °C relative to 23 °C.

conclusionAlthough time was a stronger driver than temperature of metamorphic proteome changes, temperature-induced proteome differences led to pro-growth physiology corresponding to larger oyster size at 29 °C, and to altered specific metamorphic processes and possible pathogen presence at 23 °C. These findings offer high resolution insight into why oysters may experience high mortality rates during this life transition in both field and culture settings. The proteome resource generated by this study provides data-driven guidance for future work on developmental changes in molluscs. Furthermore, the analytical approach taken here provides a foundation for effective shotgun proteomic analyses across a variety of taxa.

Indexed as

CrassostreaProteomicsAnimalsGene Expression ProfilingProteomeTemperatureProteomeDevelopmental physiologyMolluscOysterProteomicsTemperatureTime-series

Identifiers

PMID33076839
PMCPMC7574277
OpenAlexW3093043727

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.