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Light-dependent expression of a Na+/H+ exchanger 3-like transporter in the ctenidium of the giant clam, Tridacna squamosa, can be related to increased H+ excretion during light-enhanced calcification.

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TLDR
The results signify that shell formation in giant clams requires the collaboration between the ctenidium, which is a respiratory and iono‐regulatory organ, and the inner mantle, and provide new insights into the mechanisms of light‐enhanced calcification in giantClams.
Abstract
Na+/H+ exchangers (NHEs) regulate intracellular pH and ionic balance by mediating H+ efflux in exchange for Na+ uptake in a 1:1 stoichiometry. This study aimed to obtain from the ctenidium of the giant clam Tridacna squamosa ( TS ) the complete cDNA sequence of a NHE3‐like transporter ( TSNHE3 ), and to determine the effect of light exposure on its mRNA expression level and protein abundance therein. The coding sequence of TSNHE3 comprised 2886 bp, encoding 961 amino acids with an estimated molecular mass of 105.7 kDa. Immunofluorescence microscopy revealed that TSNHE3 was localized to the apical membrane of epithelial cells of the ctenidial filaments and the tertiary water channels. Particularly, the apical immunofluorescence of the ctenidial filaments was consistently stronger in the ctenidium of clams exposed to 12 h of light than those of the control kept in darkness. Indeed, light induced significant increases in the transcript level and protein abundance of TSNHE3 /TSNHE3 in the ctenidium, indicating that the transcription and translation of TSNHE3 /TSNHE3 were light‐dependent. As light‐enhanced calcification generates H+, the increased expression of TSNHE3 /TSNHE3 in the ctenidium could be a response to augment H+ excretion in pursuance of whole‐body acid‐base balance during light exposure. These results signify that shell formation in giant clams requires the collaboration between the ctenidium, which is a respiratory and iono‐regulatory organ, and the inner mantle, which is directly involved in the calcification process, and provide new insights into the mechanisms of light‐enhanced calcification in giant clams.

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Citations
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Journal ArticleDOI

The Whitish Inner Mantle of the Giant Clam, Tridacna squamosa, Expresses an Apical Plasma Membrane Ca2+-ATPase (PMCA) Which Displays Light-Dependent Gene and Protein Expressions.

TL;DR: The results support a previous proposition that symbiotic zooxanthellae, particularly those in the colorful and extensible outer mantle, may act as light-sensing elements for the host clam.
Journal ArticleDOI

Carbonic anhydrase 2-like in the giant clam, Tridacna squamosa: characterization, localization, response to light, and possible role in the transport of inorganic carbon from the host to its symbionts.

TL;DR: Cloning a CA2 homolog (CA2‐like) from the fleshy and colorful outer mantle as well as the thin and whitish inner mantle of the fluted giant clam to determine its cellular and subcellular localization, and to examine the effects of light exposure on its gene and protein expression levels.
Journal ArticleDOI

Light-dependent calcification in Red Sea giant clam Tridacna maxima

TL;DR: In this article, the authors examined the dependence of light intensity on the calcification rate of T maxima in the central Red Sea and the patterns of its abundance with depth in the field.
Journal ArticleDOI

Light exposure enhances urea absorption in the fluted giant clam, Tridacna squamosa, and up-regulates the protein abundance of a light-dependent urea active transporter, DUR3-like, in its ctenidium.

TL;DR: Light-enhanced urea absorption in the fluted giant clam, Tridacna squamosa, is demonstrated and a urea active transporter, DUR3-like, in its ctenidium is expressed which may participate in light-enhancing urease absorption.
References
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TL;DR: Using an improved method of gel electrophoresis, many hitherto unknown proteins have been found in bacteriophage T4 and some of these have been identified with specific gene products.
Journal ArticleDOI

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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Journal Article

Cleavage of structural proteins during the assemble of the head of bacterio-phage T4

U. K. Laemmli
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TL;DR: Using an improved method of gel electrophoresis, many hitherto unknown proteins have been found in bacteriophage T4 and some of these have been identified with specific gene products as mentioned in this paper.
Journal ArticleDOI

Amiloride: a molecular probe of sodium transport in tissues and cells

TL;DR: This drug is the most potent and specific inhibitor of Na+ entry found to date and thus affords the opportunity to be used as a label for the isolation of these transport moieties.
Journal ArticleDOI

Detergent binding explains anomalous SDS-PAGE migration of membrane proteins

TL;DR: The observed interdependence between hairpin migration, SDS aggregation number, and conformation suggests that detergent binding may provide a rapid and economical screen for identifying membrane proteins with robust tertiary and/or quaternary structures.
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