Characterization of 5' untranslated regions of the voltage-gated sodium channels SCN1A, SCN2A, and SCN3A and identification of cis-conserved noncoding sequences

被引:35
作者
Martin, Melinda S. [1 ]
Tang, Bin [1 ]
Ta, Nga [1 ]
Escayg, Andrew [1 ]
机构
[1] Emory Univ, Dept Human Genet, Atlanta, GA 30322 USA
关键词
epilepsy; sodium channel; SCN1A; SCN2A; SCN3A; 5' untranslated region; sequence alignment; conserved sequence; gene expression regulation;
D O I
10.1016/j.ygeno.2007.04.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
The human voltage-gated sodium channel gene cluster on chromosome 2q24 contains three paralogs, SCN1A, SCN2A, and SCN3A, which are expressed in the central nervous system. Mutations in SCN1A and SCN2A cause several subtypes of idiopathic epilepsy. Furthermore, many SCN1A mutations are predicted to reduce protein levels, emphasizing the importance of precise sodium channel gene regulation. To investigate the genetic factors that regulate the expression of SCN1A, SCN2A, and SCN3A, we characterized the 5' untranslated region of each gene. We identified multiple noncoding exons and observed brain region differences in the expression levels of noncoding exons. Comparative sequence analysis revealed 33 conserved noncoding sequences (CNSs) between the orthologous mammalian genes and 6 CNSs between the three human paralogs. Seven CNSs corresponded to noncoding exons. Twelve CNSs were evaluated for their ability to alter the transcription of a luciferase reporter gene, and 3 resulted in a modest, but statistically significant change. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:225 / 235
页数:11
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