ZFIN ID: ZDB-PUB-130605-5
Tissue-specific expression and in vivo regulation of zebrafish orthologues of mammalian genes related to symptomatic hypomagnesemia
Arjona, F.J., Chen, Y.X., Flik, G., Bindels, R.J., and Hoenderop, J.G.
Date: 2013
Source: Pflugers Archiv : European journal of physiology   465(10): 1409-21 (Journal)
Registered Authors: Arjona, F.J., Flik, Gert
Keywords: magnesium homeostasis, zebrafish, gills, kidney, gut
MeSH Terms:
  • Animals
  • Cyclins/genetics
  • Cyclins/metabolism
  • Gene Expression Regulation
  • Gills/metabolism
  • Intestines/metabolism
  • Kidney/metabolism
  • Kv1.1 Potassium Channel/genetics
  • Kv1.1 Potassium Channel/metabolism
  • Magnesium/metabolism
  • Magnesium Deficiency/genetics*
  • Magnesium Deficiency/metabolism
  • Organ Specificity
  • Potassium Channels, Inwardly Rectifying/genetics
  • Potassium Channels, Inwardly Rectifying/metabolism
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Sodium-Potassium-Exchanging ATPase/genetics
  • Sodium-Potassium-Exchanging ATPase/metabolism
  • Solute Carrier Family 12, Member 3/genetics
  • Solute Carrier Family 12, Member 3/metabolism
  • TRPM Cation Channels/genetics
  • TRPM Cation Channels/metabolism
  • Zebrafish
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
PubMed: 23636770 Full text @ Pflügers Archiv. / Eur. J. Physiol.

Introduction of zebrafish as a model for human diseases with symptomatic hypomagnesemia urges to identify the regulatory transport genes involved in zebrafish Mg2+ physiology. In humans, mutations related to hypomagnesemia are located in the genes TRPM6 and CNNM2, encoding for a Mg2+ channel and transporter, respectively; EGF (epidermal growth factor); SLC12A3, which encodes for the Na+-Cl co-transporter NCC; KCNA1 and KCNJ10, encoding for the K+ channels Kv1.1 and Kir4.1, respectively; and FXYD2, which encodes for the γ-subunit of the Na+,K+-ATPase. Orthologues of these genes were found in the zebrafish genome. For cnnm2, kcna1 and kcnj10, two conserved paralogues were retrieved. Except for fxyd2, kcna1b and kcnj10 duplicates, transcripts of orthologues were detected in ionoregulatory organs such as the gills, kidney and gut. Gene expression analyses in zebrafish acclimated to a Mg2+-deficient (0 mM Mg2+) or a Mg2+-enriched (2 mM Mg2+) water showed that branchial trpm6, gut cnnm2b and renal slc12a3 responded to ambient Mg2+. When changing the Mg2+ composition of the diet (the main source for Mg2+ in fish) to a Mg2+-deficient (0.01 % (w/w) Mg) or a Mg2+-enriched diet (0.7 % (w/w) Mg), mRNA expression of branchial trpm6, gut trpm6 and cnnm2 duplicates, and renal trpm6, egf, cnnm2a and slc12a3 was the highest in fish fed the Mg2+-deficient diet. The gene regulation patterns were in line with compensatory mechanisms to cope with Mg2+-deficiency or surplus. Our findings suggest that trpm6, egf, cnnm2 paralogues and slc12a3 are involved in the in vivo regulation of Mg2+ transport in ionoregulatory organs of the zebrafish model.