Expression of calcification‐related ion transporters during blue mussel larval development

Abstract The physiological processes driving the rapid rates of calcification in larval bivalves are poorly understood. Here, we use a calcification substrate‐limited approach (low dissolved inorganic carbon, CT) and mRNA sequencing to identify proteins involved in bicarbonate acquisition during she...

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Main Authors: Kirti Ramesh, Tejaswi Yarra, Melody S. Clark, Uwe John, Frank Melzner
Format: Article
Language:English
Published: Wiley 2019-06-01
Series:Ecology and Evolution
Subjects:
Online Access:https://doi.org/10.1002/ece3.5287
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author Kirti Ramesh
Tejaswi Yarra
Melody S. Clark
Uwe John
Frank Melzner
author_facet Kirti Ramesh
Tejaswi Yarra
Melody S. Clark
Uwe John
Frank Melzner
author_sort Kirti Ramesh
collection DOAJ
description Abstract The physiological processes driving the rapid rates of calcification in larval bivalves are poorly understood. Here, we use a calcification substrate‐limited approach (low dissolved inorganic carbon, CT) and mRNA sequencing to identify proteins involved in bicarbonate acquisition during shell formation. As a secondary approach, we examined expression of ion transport and shell matrix proteins (SMPs) over the course of larval development and shell formation. We reared four families of Mytilus edulis under ambient (ca. 1865 µmol/kg) and low CT (ca. 941 µmol/kg) conditions and compared expression patterns at six developmental time points. Larvae reared under low CT exhibited a developmental delay, and a small subset of contigs was differentially regulated between ambient and low CT conditions. Of particular note was the identification of one contig encoding an anion transporter (SLC26) which was strongly upregulated (2.3–2.9 fold) under low CT conditions. By analyzing gene expression profiles over the course of larval development, we are able to isolate sequences encoding ion transport and SMPs to enhance our understanding of cellular pathways underlying larval calcification processes. In particular, we observe the differential expression of contigs encoding SLC4 family members (sodium bicarbonate cotransporters, anion exchangers), calcium‐transporting ATPases, sodium/calcium exchangers, and SMPs such as nacrein, tyrosinase, and transcripts related to chitin production. With a range of candidate genes, this work identifies ion transport pathways in bivalve larvae and by applying comparative genomics to investigate temporal expression patterns, provides a foundation for further studies to functionally characterize the proteins involved in larval calcification.
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spelling doaj.art-ba6a9db950c14d9b81ec5487aab8257e2022-12-21T23:53:24ZengWileyEcology and Evolution2045-77582019-06-019127157717210.1002/ece3.5287Expression of calcification‐related ion transporters during blue mussel larval developmentKirti Ramesh0Tejaswi Yarra1Melody S. Clark2Uwe John3Frank Melzner4GEOMAR Helmholtz Centre for Ocean Research Kiel GermanyBritish Antarctic Survey Natural Environment Research Council Cambridge UKBritish Antarctic Survey Natural Environment Research Council Cambridge UKEcological Chemistry Alfred‐Wegener‐Institut Helmholtz‐Zentrum für Polar‐und Meeresforschung Bremerhaven GermanyGEOMAR Helmholtz Centre for Ocean Research Kiel GermanyAbstract The physiological processes driving the rapid rates of calcification in larval bivalves are poorly understood. Here, we use a calcification substrate‐limited approach (low dissolved inorganic carbon, CT) and mRNA sequencing to identify proteins involved in bicarbonate acquisition during shell formation. As a secondary approach, we examined expression of ion transport and shell matrix proteins (SMPs) over the course of larval development and shell formation. We reared four families of Mytilus edulis under ambient (ca. 1865 µmol/kg) and low CT (ca. 941 µmol/kg) conditions and compared expression patterns at six developmental time points. Larvae reared under low CT exhibited a developmental delay, and a small subset of contigs was differentially regulated between ambient and low CT conditions. Of particular note was the identification of one contig encoding an anion transporter (SLC26) which was strongly upregulated (2.3–2.9 fold) under low CT conditions. By analyzing gene expression profiles over the course of larval development, we are able to isolate sequences encoding ion transport and SMPs to enhance our understanding of cellular pathways underlying larval calcification processes. In particular, we observe the differential expression of contigs encoding SLC4 family members (sodium bicarbonate cotransporters, anion exchangers), calcium‐transporting ATPases, sodium/calcium exchangers, and SMPs such as nacrein, tyrosinase, and transcripts related to chitin production. With a range of candidate genes, this work identifies ion transport pathways in bivalve larvae and by applying comparative genomics to investigate temporal expression patterns, provides a foundation for further studies to functionally characterize the proteins involved in larval calcification.https://doi.org/10.1002/ece3.5287biomineralizationbivalvesgene expressionlarvae
spellingShingle Kirti Ramesh
Tejaswi Yarra
Melody S. Clark
Uwe John
Frank Melzner
Expression of calcification‐related ion transporters during blue mussel larval development
Ecology and Evolution
biomineralization
bivalves
gene expression
larvae
title Expression of calcification‐related ion transporters during blue mussel larval development
title_full Expression of calcification‐related ion transporters during blue mussel larval development
title_fullStr Expression of calcification‐related ion transporters during blue mussel larval development
title_full_unstemmed Expression of calcification‐related ion transporters during blue mussel larval development
title_short Expression of calcification‐related ion transporters during blue mussel larval development
title_sort expression of calcification related ion transporters during blue mussel larval development
topic biomineralization
bivalves
gene expression
larvae
url https://doi.org/10.1002/ece3.5287
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