Regulation of gene expression in adeno-associated virus vectors in the brain

被引:19
作者
Haberman, RP [1 ]
McGown, TJ
机构
[1] Univ N Carolina, Gene Therapy Ctr, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Psychiat, Chapel Hill, NC 27599 USA
关键词
inducible; gene therapy; central nervous system; tetracycline; tropism; promoter;
D O I
10.1016/S1046-2023(02)00226-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Regulated adeno-associated virus (AAV) vectors have broad utility in both experimental and applied gene therapy. and to date, several regulation systems have exhibited a capability to control gene expression from viral vectors over two orders of magnitude. The tetracycline responsive system has been the most used in AAV, although other regulation systems such as RU486- and rapamycin-responsive systems are reasonable options. AAV vectors influence how regulation systems function by several mechanisms, leading to increased background gene expression and restricted induction. Methods to reduce background expression continue to be explored and systems not yet tried in AAV may prove quite functional. Although regulated promoters are often assumed to exhibit ubiquitous expression. the tropism of different neuronal subtypes can be altered dramatically by changing promoters in recombinant AAV vectors. Differences in promoter-directed tropism have significant consequences for proper expression of gene products as well as the utility of dual vector regulation. Thus regulated vector systems must be carefully optimized for each application. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:219 / 226
页数:8
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