Evolution of sodium channel genes
Evolution of sodium channel genes
批准号:
8100484
负责人:
HAROLD H ZAKON
金额:
$29.09万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-07-01 至 2013-06-30
关键词:
Amino Acid SubstitutionAmino AcidsBase SequenceBioinformaticsC-terminalCloningCommunicationData SetDiseaseElectric FishElectric OrganEtiologyEventEvolutionFamilyFishesFrequenciesGenesHeart DiseasesHumanIn Situ HybridizationIon ChannelLearningMeasuresMethodsModificationMuscleMuscle FibersMutationMyopathyNeuronsOrganismPacemakersPatternPolymerase Chain ReactionProcessPropertyProteinsRelative (related person)SamplingSeminalSequence AnalysisSiteSite-Directed MutagenesisSodiumSodium ChannelTestingTimeVertebratesWorkXenopus oocytecopingimprovedinsightinterestnervous system disordernovelpressureteleostvoltage
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Mutations in voltage-dependent sodium channel genes cause neurological, muscular, and cardiac diseases. Although much is known about sodium channel function, there is still much to learn. The sodium channel is a large molecule and understanding which of its many amino acids is important to its function is a daunting task. One method to pinpoint potentially important amino acids in a protein is to align the sequences of the same protein from a number of different organisms to find out which amino acids do NOT change over the course of evolution. Another lesser-used strategy that we employ here is to include sequences from organisms in which that molecule is under strong selection pressure to evolve. In this case, we look for amino acid changes that DO change over the course of evolution. Weakly electric fish generate electric organ discharges (EODs) for communication and sensing objects. EODs are generated by sodium channels and the sodium channels of electric fish have undergone strong selection for species-specific changes in amino acids in critical regions of the channel. Using the approach described above, we have already discovered a novel functional domain of sodium channels. We will continue to study the process of evolution of sodium channel genes in the two independently evolved groups of electric fish in order to discover other functionally important regions of the channel. Using bioinformatics approaches to compare amino acid and nucleotide sequences in the two groups of electric fish, non-electric fish, and other vertebrates, including humans, we will detect amino acids sites that are likely under positive selection in the electric fish's sodium channels. We will then test whether these particular amino acids are truly important to channel function by introducing the amino acid changes that we observe in electric fish sodium channels into a human muscle sodium channel (as well as the converse) and determining whether these alter the biophysical properties of expressed sodium channels. Besides providing insights into the evolutionary processes, this work will aid our basic understanding of the functioning of sodium channels, a clinically important family of ion channels.
Project Narrative: Mutations in sodium channel genes cause neurological, muscular, and cardiac diseases. Using bioinformatics approaches we will identify amino acids that are likely to be important to the function of the sodium channel. We will then test whether these particular amino acids are truly important to channel function by perturbing these amino acid in a human muscle sodium channel gene and observing whether these alter the biophysical properties of the sodium channels. This work will be medically important to understand the function of sodium channels, a clinically important family of ion channels.
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DOI:
10.1126/science.1254432
发表时间:
2014-06-27
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
[Gallant JR, Traeger LL, Volkening JD, Moffett H, Chen PH, Novina CD, Phillips GN Jr, Anand R, Wells GB, Pinch M, Güth R, Unguez GA, Albert JS, Zakon HH, Samanta MP, Sussman MR]
通讯作者:
Sussman MR
Expansion of voltage-dependent Na+ channel gene family in early tetrapods coincided with the emergence of terrestriality and increased brain complexity.
早期四足动物中电压依赖性Na通道基因家族的扩展与陆地性的出现和大脑复杂性的增加同时发生。
DOI:
10.1093/molbev/msq325
发表时间:
2011
期刊:
Molecular biology and evolution
影响因子:
10.7
作者:
[Zakon,HaroldH, Jost,MandaC, Lu,Ying]
通讯作者:
Lu,Ying
Evolution of sodium channels and the new view of early nervous system evolution.
钠通道的进化和早期神经系统进化的新观点。
DOI:
10.4161/cib.17069
发表时间:
2011
期刊:
Communicative & integrative biology
影响因子:
--
作者:
[Liebeskind,BenjaminJ]
通讯作者:
Liebeskind,BenjaminJ
DOI:
10.1186/s12864-015-1288-8
发表时间:
2015-03-26
期刊:
BMC genomics
影响因子:
4.4
作者:
[Traeger LL, Volkening JD, Moffett H, Gallant JR, Chen PH, Novina CD, Phillips GN Jr, Anand R, Wells GB, Pinch M, Güth R, Unguez GA, Albert JS, Zakon H, Sussman MR, Samanta MP]
通讯作者:
Samanta MP
Evolution of sodium channel genes
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批准号:7868838
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项目类别:
-
资助金额:$27.14万
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财政年份:2009
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负责人:HAROLD H ZAKON
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依托单位:
Evolution of sodium channel genes
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批准号:7635770
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项目类别:
-
资助金额:$29.68万
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财政年份:2008
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负责人:HAROLD H ZAKON
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依托单位:
Evolution of sodium channel genes
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批准号:7526885
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项目类别:
-
资助金额:$29.68万
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财政年份:2008
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负责人:HAROLD H ZAKON
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依托单位:
Evolution of sodium channel genes
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批准号:7884118
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项目类别:
-
资助金额:$29.38万
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财政年份:2008
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负责人:HAROLD H ZAKON
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依托单位:
Gordon Research Conference on Neuroethology
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批准号:6458669
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项目类别:
-
资助金额:$2.8万
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财政年份:2002
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负责人:HAROLD H ZAKON
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依托单位:
SENSORY RECALIBRATION OF MOTOR OUTPUT
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批准号:6477052
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项目类别:
-
资助金额:$22.5万
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财政年份:1996
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负责人:HAROLD H ZAKON
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依托单位:
NEURAL BASIS OF PLASTICITY
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批准号:2839197
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项目类别:
-
资助金额:$10.33万
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财政年份:1996
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负责人:HAROLD H ZAKON
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依托单位:
SENSORY RECALIBRATION OF MOTOR OUTPUT
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批准号:6625393
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项目类别:
-
资助金额:$22.5万
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财政年份:1996
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负责人:HAROLD H ZAKON
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依托单位:
NEURAL BASIS OF PLASTICITY
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批准号:2035192
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项目类别:
-
资助金额:$11.53万
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财政年份:1996
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负责人:HAROLD H ZAKON
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依托单位:
SENSORY RECALIBRATION OF MOTOR OUTPUT
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批准号:6683639
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项目类别:
-
资助金额:$22.5万
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财政年份:1996
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负责人:HAROLD H ZAKON
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依托单位:
NEURAL BASIS OF PLASTICITY
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批准号:2609482
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项目类别:
-
资助金额:$10.03万
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财政年份:1996
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负责人:HAROLD H ZAKON
-
依托单位:
SENSORY RECALIBRATION OF MOTOR OUTPUT
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批准号:6292405
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项目类别:
-
资助金额:$31.25万
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财政年份:1996
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负责人:HAROLD H ZAKON
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依托单位:
INNERVATION AND ELECTRORECEPTOR REGENERATION
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批准号:2126549
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项目类别:
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资助金额:$7.65万
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财政年份:1992
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负责人:HAROLD H ZAKON
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依托单位:
ROLE OF INNERVATION IN ELECTRORECEPTOR REGENERATION
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批准号:3218142
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项目类别:
-
资助金额:$7.31万
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财政年份:1992
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负责人:HAROLD H ZAKON
-
依托单位:
ROLE OF INNERVATION IN ELECTRORECEPTOR REGENERATION
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批准号:3218141
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项目类别:
-
资助金额:$8.78万
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财政年份:1992
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负责人:HAROLD H ZAKON
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依托单位:
HORMONAL MODULATION OF A COMMUNICATION SIGNAL
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批准号:6343827
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项目类别:
-
资助金额:$28.3万
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财政年份:1989
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负责人:HAROLD H ZAKON
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依托单位:
HORMONAL MODULATION OF A COMMUNICATION SIGNAL
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批准号:6322606
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项目类别:
-
资助金额:$2.5万
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财政年份:1989
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负责人:HAROLD H ZAKON
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依托单位:
HORMONAL MODULATION OF A COMMUNICATION SIGNAL
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批准号:2265559
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项目类别:
-
资助金额:$12.58万
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财政年份:1989
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负责人:HAROLD H ZAKON
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依托单位:
Hormonal modulation of a communication signal
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批准号:6893407
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项目类别:
-
资助金额:$34.69万
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财政年份:1989
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负责人:HAROLD H ZAKON
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依托单位:
Hormonal modulation of a communication signal
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批准号:7067166
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项目类别:
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资助金额:$33.87万
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财政年份:1989
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负责人:HAROLD H ZAKON
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依托单位:
海外基金