Developmentally regulated expression of the mouse homologues of the potassium channel encoding genes m-erg1, m-erg2 and m-erg3

被引:23
作者
Polvani, S
Masi, A
Pillozzi, S
Gragnani, L
Crociani, O
Olivotto, M
Becchetti, A
Wanke, E
Arcangeli, A
机构
[1] Univ Florence, Dept Expt Pathol & Oncol, I-50134 Florence, Italy
[2] Univ Milano Bicocca, Dept Biotechol & Biosci, I-20126 Milan, Italy
关键词
neuromuscular excitability; cellular excitability; expression pattern; mouse embryo; embryo development; potassium channels; ERG; m-erg1; m-erg2; m-erg3; whole-mount in situ hybridisation;
D O I
10.1016/S1567-133X(03)00124-8
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Deciphering the expression pattern of K+ channel encoding genes during development can help in the understanding of the establishment of cellular excitability and unravel the molecular mechanisms of neuromuscular diseases. We focused our attention on genes belonging to the erg family, which is deeply involved in the control of neuromuscular excitability in Drosophila flies and possibly other organisms. Both in situ hybridisation and RNase Protection Assay experiments were used to study the expression pattern of mouse (m)erg1, m-erg2 and m-erg3 genes during mouse embryo development, to allow the pattern to be compared with their expression in the adult. M-erg1 is first expressed in the heart and in the central nervous system (CNS) of embryonic day 9.5 (E9.5) embryos; the gene appears in ganglia of the peripheral nervous system (PNS) (dorsal root (DRG) and sympathetic (SCG) ganglia, mioenteric plexus), in the neural layer of retina, skeletal muscles, gonads and gut at E13.5. In the adult m-erg1 is expressed in the heart, various structures of the CNS, DRG and retina. M-erg2 is first expressed at E9.5 in the CNS, thereafter (E13.5) in the neural layer of retina, DRG, SCG, and in the atrium. In the adult the gene is present in some restricted areas of the CNS, retina and DRG. M-erg3 displayed an expression pattern partially overlapping that of m-erg1, with a transitory expression in the developing heart as well. A detailed study of the mouse adult brain showed a peculiar expression pattern of the three genes, sometimes overlapping in different encephalic areas. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:767 / 776
页数:10
相关论文
共 18 条
[1]   HERG- and IRK-like inward rectifier currents are sequentially expressed during neuronal development of neural crest cells and their derivatives [J].
Arcangeli, A ;
Rosati, B ;
Cherubini, A ;
Crociani, O ;
Fontana, L ;
Ziller, C ;
Wanke, E ;
Olivotto, M .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1997, 9 (12) :2596-2604
[2]   A novel inward-rectifying K+ current with a cell-cycle dependence governs the resting potential of mammalian neuroblastoma cells [J].
Arcangeli, A ;
Bianchi, L ;
Becchetti, A ;
Faravelli, L ;
Coronnello, M ;
Mini, E ;
Olivotto, M ;
Wanke, E .
JOURNAL OF PHYSIOLOGY-LONDON, 1995, 489 (02) :455-471
[3]  
Bianchi L, 1998, CANCER RES, V58, P815
[4]  
Braissant O., 1998, BIOCHEMICA, V1, P10
[5]   Cell cycle-dependent expression of HERG1 and HERG1B isoforms in tumor cells [J].
Crociani, O ;
Guasti, L ;
Balzi, M ;
Becchetti, A ;
Wanke, E ;
Olivotto, M ;
Wymore, RS ;
Arcangeli, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (05) :2947-2955
[6]   erg gene(s) expression during development of the nervous and muscular system of quail embryos [J].
Crociani, O ;
Cherubini, A ;
Piccini, E ;
Polvani, S ;
Costa, L ;
Fontana, L ;
Hofmann, G ;
Rosati, B ;
Wanke, E ;
Olivotto, M ;
Arcangeli, A .
MECHANISMS OF DEVELOPMENT, 2000, 95 (1-2) :239-243
[7]   A MOLECULAR-BASIS FOR CARDIAC-ARRHYTHMIA - HERG MUTATIONS CAUSE LONG QT SYNDROME [J].
CURRAN, ME ;
SPLAWSKI, I ;
TIMOTHY, KW ;
VINCENT, GM ;
GREEN, ED ;
KEATING, MT .
CELL, 1995, 80 (05) :795-803
[8]   QUANTITATIVE-ANALYSIS OF POTASSIUM CHANNEL MESSENGER-RNA EXPRESSION IN ATRIAL AND VENTRICULAR MUSCLE OF RATS [J].
DIXON, JE ;
MCKINNON, D .
CIRCULATION RESEARCH, 1994, 75 (02) :252-260
[9]   Divergent expression of delayed rectifier K+ channel subunits during mouse heart development [J].
Franco, D ;
Demolombe, S ;
Kupershmidt, S ;
Dumaine, R ;
Dominguez, JN ;
Roden, D ;
Antzelevitch, C ;
Escande, D ;
Moorman, AFM .
CARDIOVASCULAR RESEARCH, 2001, 52 (01) :65-75
[10]  
London B, 1997, CIRC RES, V81, P870