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基因的小胶质细胞特异性启动子活性

Microglia-Specific Promoter Activities of Gene.

作者信息

Shah Sahil, Wong Lilly M, Ellis Kendra, Bodnar Brittany, Saribas Sami, Ting Julia, Wei Zhengyu, Tang Yuyang, Wang Xianwei, Wang Hong, Ling Binhua, Margolis David M, Garcia J Victor, Hu Wenhui, Jiang Guochun

机构信息

Center for Metabolic Disease Research, Temple University Lewis Katz School of Medicine, Philadelphia, PA, United States.

Department of Pathology and Laboratory Medicine, Temple University Lewis Katz School of Medicine, Philadelphia, PA, United States.

出版信息

Front Cell Neurosci. 2022 Mar 10;16:808598. doi: 10.3389/fncel.2022.808598. eCollection 2022.

Abstract

Adeno-associated virus (AAV)-mediated genetic targeting of microglia remains a challenge. Overcoming this hurdle is essential for gene editing in the central nervous system (CNS). Here, we characterized the minimal/native promoter of the gene, which is known to be specifically and stably expressed in the microglia during homeostatic and pathological conditions. Dual reporter and serial deletion assays identified the critical role of the natural 5' untranslated region (-97 bp related to the first ATG) in driving transcriptional activity of the mouse gene. The native promoter region of mouse, human, and monkey are located at -135, -134, and -170 bp to the first ATG, respectively. These promoters were highly active and specific in microglia with strong cross-species transcriptional activities, but did not exhibit activity in primary astrocytes. In addition, we identified a 135 bp promoter of gene that was highly active in microglia but not in astrocytes. Considering that is specifically expressed in microglia, these data suggest that the newly characterized microglia-specific minimal/native promoter can be an ideal candidate for microglia-targeting AAV gene therapy in the CNS.

摘要

腺相关病毒(AAV)介导的小胶质细胞基因靶向仍然是一个挑战。克服这一障碍对于中枢神经系统(CNS)中的基因编辑至关重要。在此,我们对该基因的最小/天然启动子进行了表征,已知该启动子在稳态和病理条件下在小胶质细胞中特异性且稳定地表达。双报告基因和序列缺失分析确定了天然5'非翻译区(与第一个ATG相关的-97 bp)在驱动小鼠基因转录活性中的关键作用。小鼠、人类和猴子的天然启动子区域分别位于第一个ATG的-135、-134和-170 bp处。这些启动子在小胶质细胞中具有高活性和特异性,具有很强的跨物种转录活性,但在原代星形胶质细胞中不表现出活性。此外,我们鉴定了一个在小胶质细胞中高活性但在星形胶质细胞中无活性的135 bp基因启动子。鉴于该基因在小胶质细胞中特异性表达,这些数据表明新表征的小胶质细胞特异性最小/天然启动子可能是中枢神经系统中小胶质细胞靶向AAV基因治疗的理想候选者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e242/8960132/72fa8dd3d10e/fncel-16-808598-g001.jpg

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