Tocotrienols induce IKBKAP expression:: a possible therapy for familial dysautonomia

被引:54
作者
Anderson, SL [1 ]
Qiu, JS [1 ]
Rubin, BY [1 ]
机构
[1] Fordham Univ, Dept Biol Sci, Lab Familial Dysautonomia Res, Bronx, NY 10458 USA
关键词
familial dysautonomia; IKAP; IKBKAP; tocotrienol; vitamin E;
D O I
10.1016/S0006-291X(03)00971-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Familial dysautonomia (FD), a neurodegenerative genetic disorder primarily affecting individuals of Ashkenazi Jewish descent, is caused by mutations in the IKBKAP gene which encodes the IkappaB kinase complex-associated protein (IKAP). The more common or major mutation causes aberrant splicing, resulting in a truncated form of IKAP. Tissues from individuals homozygous for the major mutation contain both mutant and wild-type IKAP transcripts. The apparent leaky nature of this mutation prompted a search for agents capable of elevating the level of expression of the wild-type IKAP transcript. We report the ability of tocotrienols, members of the vitamin E family, to increase transcription of IKAP mRNA in FD-derived cells, with corresponding increases in the correctly spliced transcript and normal protein. These findings suggest that in vivo supplementation with tocotrienols may elevate IKBKAP gene expression and in turn increase the amount of functional IKAP protein produced in FD patients. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:303 / 309
页数:7
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