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从小细胞通用启动子在小鼠大脑中观察到的长期 AAV 载体基因和蛋白表达与神经细胞启动子相似。

Long-term AAV vector gene and protein expression in mouse brain from a small pan-cellular promoter is similar to neural cell promoters.

机构信息

W F Goodman Center for Comparative Medical Genetics, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Gene Ther. 2009 Jul;16(7):927-32. doi: 10.1038/gt.2009.52. Epub 2009 May 21.

Abstract

The neurogenetic, lysosomal enzyme (LSE) deficiency diseases are characterized by storage lesions throughout the brain; therefore, gene transfer needs to provide widespread distribution of the normal enzyme. Adeno-associated virus (AAV) vectors can be effective in the brain despite limited transduction because LSEs are exported to neighboring cells (cross-correction) to reverse the metabolic deficit. The extent of correction is determined by a combination of the total amount of LSE produced by a vector and the spatial distribution of the vector within the brain. Neuron-specific promoters have been used in the brain because AAV predominantly transduces neurons. However, these promoters are large, using up a substantial amount of the limited cloning capacity of AAV vector genomes. A small promoter that is active in all cells, from the LSE beta-glucuronidase (GUSB), has been used for long-term expression in AAV vectors in the brain but the natural promoter is expressed at very low levels. The amount of LSE exported from a cell is proportional to the level of transcription, thus more active promoters would export more LSE for cross-correction, but direct comparisons have not been reported. In this study, we show that in long-term experiments (>6 months) the GUSB minimal promoter (hGBp) expresses the hGUSB enzyme in brain at similar levels as the neuron-specific enolase promoter or the promoter from the latency-associated transcript of herpes simplex virus. The hGBp minimal promoter thus may be useful for long-term expression in the central nervous system of large cDNAs, bicitronic transcription units, self-complimentary or other designs with size constraints in the AAV vector system.

摘要

神经遗传、溶酶体酶 (LSE) 缺乏症的特征是大脑中存在储存病变;因此,基因转移需要提供正常酶的广泛分布。尽管腺相关病毒 (AAV) 载体的转导有限,但由于 LSE 会被输出到邻近细胞(交叉校正)以逆转代谢缺陷,因此它们在大脑中可以很有效。校正的程度取决于载体产生的 LSE 总量和载体在大脑内的空间分布的组合。神经元特异性启动子已被用于大脑中,因为 AAV 主要转导神经元。然而,这些启动子很大,占用了 AAV 载体基因组有限克隆容量的很大一部分。一个在所有细胞中都活跃的小启动子,即 LSE β-葡糖苷酸酶 (GUSB),已被用于大脑中的 AAV 载体进行长期表达,但天然启动子的表达水平非常低。细胞中输出的 LSE 量与转录水平成正比,因此更活跃的启动子会输出更多的 LSE 进行交叉校正,但尚未报道直接比较。在这项研究中,我们表明,在长期实验 (>6 个月) 中,GUSB 最小启动子 (hGBp) 以与神经元特异性烯醇化酶启动子或单纯疱疹病毒潜伏相关转录物的启动子相似的水平在大脑中表达 hGUSB 酶。因此,hGBp 最小启动子可能可用于 AAV 载体系统中具有大小限制的大 cDNA、双顺反子转录单元、自我互补或其他设计在中枢神经系统中的长期表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac0c/5473363/ae56343c8cd5/nihms-154217-f0001.jpg

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