Naturally Occurring Deletion Mutants of the Pig-Specific, Intestinal Crypt Epithelial Cell Protein CLCA4b without Apparent Phenotype
Stephanie Plog, Nikolai Klymiuk, Stefanie Binder, Matthew J. Van Hook, Wallace B. Thoreson, Achim D. Gruber, Lars Mundhenk

TL;DR
This study explores a pig-specific protein, CLCA4b, and its role in the intestines, finding that a deletion mutation does not cause noticeable effects.
Contribution
The study identifies a naturally occurring deletion mutant of CLCA4b in pigs with no apparent phenotype.
Findings
CLCA4b is a pig-specific gene expressed in intestinal crypt epithelial cells.
A deleterious mutation in CLCA4b is common in pig breeds but does not cause a visible phenotype.
CLCA4b does not produce a calcium-activated anion conductance like other CLCA proteins.
Abstract
The human CLCA4 (chloride channel regulator, calcium-activated) modulates the intestinal phenotype of cystic fibrosis (CF) patients via an as yet unknown pathway. With the generation of new porcine CF models, species-specific differences between human modifiers of CF and their porcine orthologs are considered critical for the translation of experimental data. Specifically, the porcine ortholog to the human CF modulator gene CLCA4 has recently been shown to be duplicated into two separate genes, CLCA4a and CLCA4b. Here, we characterize the duplication product, CLCA4b, in terms of its genomic structure, tissue and cellular expression patterns as well as its in vitro electrophysiological properties. The CLCA4b gene is a pig-specific duplication product of the CLCA4 ancestor and its protein is exclusively expressed in small and large intestinal crypt epithelial cells, a niche specifically…
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Taxonomy
TopicsInflammatory mediators and NSAID effects · Antiplatelet Therapy and Cardiovascular Diseases · Hormonal Regulation and Hypertension
