TY - JOUR
T1 - Functional characterisation and genomic analysis of an epithelial calcium channel (ECaC) from pufferfish, Fugu rubripes
AU - Qiu, A D
AU - Hogstrand, C
PY - 2004/11/1
Y1 - 2004/11/1
N2 - An orthologue to the mammalian epithelia] calcium channels, ECaC1 (TRPV5) and ECaC2 (TRPV6), was cloned from gill of pufferfish (Fugu rubripes) and characterised, demonstrating that this gene predates the evolution of land-living vertebrates. The F rubripes ECaC (FrECaC) protein displays all structural features typical for mammalian ECaCs including three ankyrin repeats, six transmembrane domains, and a putative pore region between TM V and TM VI. Functional expression of FrECaC in Madin-Darby canine kidney (MDCK) cells confirmed that the channel mediates Ca2+ influx. FrECaC was also permeable to Zn2+ and, to a small extent, to the Fe2+ ion. Thus, in addition to a role in Ca2+ uptake FrECaC might serve as a pathway for zinc and iron acquisition. FrECaC mRNA was highly abundant in the gill, but sparsely present in the intestine. Calcium absorption via FrECaC in pufferfish may be subject to the regulation of 1,25(OH)(2)D-3, estrogen and progesterone as consensus cis regulatory elements for the respective steroid hormone receptors were found in the upstream regulatory region of the FrECaC gene. FrECaC gene organisation is very conserved when compared with mammalian ECaCs. Only one ECaC gene seems to exist in the F rubripes genome, and the corresponding protein clusters together with ECaC2 from mammals upon phylogenetic analysis. Thus, the two mammalian ECaC genes may,originate from a single ancestral ECaC2 gene in vertebrates appearing early in evolution. (C) 2004 Elsevier B.V. All rights reserved.
AB - An orthologue to the mammalian epithelia] calcium channels, ECaC1 (TRPV5) and ECaC2 (TRPV6), was cloned from gill of pufferfish (Fugu rubripes) and characterised, demonstrating that this gene predates the evolution of land-living vertebrates. The F rubripes ECaC (FrECaC) protein displays all structural features typical for mammalian ECaCs including three ankyrin repeats, six transmembrane domains, and a putative pore region between TM V and TM VI. Functional expression of FrECaC in Madin-Darby canine kidney (MDCK) cells confirmed that the channel mediates Ca2+ influx. FrECaC was also permeable to Zn2+ and, to a small extent, to the Fe2+ ion. Thus, in addition to a role in Ca2+ uptake FrECaC might serve as a pathway for zinc and iron acquisition. FrECaC mRNA was highly abundant in the gill, but sparsely present in the intestine. Calcium absorption via FrECaC in pufferfish may be subject to the regulation of 1,25(OH)(2)D-3, estrogen and progesterone as consensus cis regulatory elements for the respective steroid hormone receptors were found in the upstream regulatory region of the FrECaC gene. FrECaC gene organisation is very conserved when compared with mammalian ECaCs. Only one ECaC gene seems to exist in the F rubripes genome, and the corresponding protein clusters together with ECaC2 from mammals upon phylogenetic analysis. Thus, the two mammalian ECaC genes may,originate from a single ancestral ECaC2 gene in vertebrates appearing early in evolution. (C) 2004 Elsevier B.V. All rights reserved.
UR - http://www.scopus.com/inward/record.url?scp=7644223075&partnerID=8YFLogxK
U2 - 10.1016/j.gene.2004.07.041
DO - 10.1016/j.gene.2004.07.041
M3 - Article
VL - 342
SP - 113
EP - 123
JO - Gene
JF - Gene
IS - 1
ER -