Evolution tunes the excitability of individual neurons

被引:41
作者
Salkoff, L
Butler, A
Fawcett, G
Kunkel, M
McArdle, C
Paz-y-Mino, G
Nonet, M
Walton, N
Wang, ZW
Yuan, A
Wei, A
机构
[1] Washington Univ, Sch Med, Dept Anat & Neurobiol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
potassium channels; genes; TWIK; task; C; elegans; evolution;
D O I
10.1016/S0306-4522(01)00079-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The relationship between the genome and the evolution of the nervous system may differ between an animal like C, elegans with 302 neurons, and mammals with tens of billions of neurons. Here we report that a class of nonconserved potassium channels highly expanded in C, elegans may play a special role in the evolution of its nervous system. The C, elegans genome contains an extended gene family of potassium channels whose members fall into two evolutionary divergent classes. One class constitutes an ancient conserved "set" of K+ channels with orthologues in both humans and Drosophila(1,24) and a second larger class made up of rapidly evolving genes unique to C, elegans.(24) Chief among this second class are novel potassium channels having four transmembrane domains per subunit(6,8,14,20) that function as regulated leak conductances to modulate cell electrical excitability. This inventory of novel potassium channels is far larger in C. elegans than in humans or Drosophila, We found that, unlike conserved channel genes, the majority of these genes are expressed in very few cells. We also identified DNA enhancer elements associated with these genes that direct gene expression to individual neurons. We conclude that C, elegans may maintain an exceptionally large inventory of these channels (as well as ligand-gated channels') as an adaptive mechanism to "fine tune" individual neurons, making the most of its limited circuitry. (C) 2001 IBRO. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:853 / 859
页数:7
相关论文
共 27 条
[1]   Neurobiology of the Caenorhabditis elegans genome [J].
Bargmann, CI .
SCIENCE, 1998, 282 (5396) :2028-2033
[2]   Adaptive regulation of neuronal excitability by a voltage-independent potassium conductance [J].
Brickley, SG ;
Revilla, V ;
Cull-Candy, SG ;
Wisden, W ;
Farrant, M .
NATURE, 2001, 409 (6816) :88-92
[3]   Building a dictionary for genomes: Identification of presumptive regulatory sites by statistical analysis [J].
Bussemaker, HJ ;
Li, H ;
Siggia, ED .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (18) :10096-10100
[4]   MSLO, A COMPLEX MOUSE GENE ENCODING MAXI CALCIUM-ACTIVATED POTASSIUM CHANNELS [J].
BUTLER, A ;
TSUNODA, S ;
MCCOBB, DP ;
WEI, A ;
SALKOFF, L .
SCIENCE, 1993, 261 (5118) :221-224
[5]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[6]   TASK, a human background K+ channel to sense external pH variations near physiological pH [J].
Duprat, F ;
Lesage, F ;
Fink, M ;
Reyes, R ;
Heurteaux, C ;
Lazdunski, M .
EMBO JOURNAL, 1997, 16 (17) :5464-5471
[7]   Functional genomics [J].
Fields, S ;
Kohara, Y ;
Lockhart, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (16) :8825-8826
[8]   Sequence and function of the two P domain potassium channels: Implications of an emerging superfamily [J].
Goldstein, SAN ;
Wang, KW ;
Ilan, N ;
Pausch, MH .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1998, 76 (01) :13-20
[9]   Cloned potassium channels from eukaryotes and prokaryotes [J].
Jan, LY ;
Jan, YN .
ANNUAL REVIEW OF NEUROSCIENCE, 1997, 20 :91-123
[10]   CHARACTERIZATION OF TISSUE-EXPRESSED ALPHA-SUBUNITS OF THE HIGH-CONDUCTANCE CA2+-ACTIVATED K+ CHANNEL [J].
KNAUS, HG ;
EBERHART, A ;
KOCH, ROA ;
MUNUJOS, P ;
SCHMALHOFER, WA ;
WARMKE, JW ;
KACZOROWSKI, GJ ;
GARCIA, ML .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (38) :22434-22439