Department of Biochemistry, Boston University School of Medicine, Boston, MA, USA.
Klogene Therapeutics, Inc., Boston, MA, USA.
J Mol Neurosci. 2018 Feb;64(2):175-184. doi: 10.1007/s12031-017-1011-0. Epub 2018 Jan 19.
Multiple lines of evidence show that the anti-aging and cognition-enhancing protein Klotho fosters neuronal survival, increases the anti-oxidative stress defense, and promotes remyelination of demyelinated axons. Thus, upregulation of the Klotho gene can potentially alleviate the symptoms and/or prevent the progression of age-associated neurodegenerative diseases such as Alzheimer's disease and demyelinating diseases such as multiple sclerosis. Here we used a CRISPR-dCas9 complex to investigate single-guide RNA (sgRNA) targeting the Klotho promoter region for efficient transcriptional activation of the Klotho gene. We tested the sgRNAs within the - 1 to - 300 bp of the Klotho promoter region and identified two sgRNAs that can effectively enhance Klotho gene transcription. We examined the transcriptional activation of the Klotho gene using three different systems: a Firefly luciferase (FLuc) and NanoLuc luciferase (NLuc) coincidence reporter system, a NLuc knock-in in Klotho 3'-UTR using CRISPR genomic editing, and two human cell lines: neuronal SY5Y cells and kidney HK-2 cells that express Klotho endogenously. The two sgRNAs enhanced Klotho expression at both the gene and protein levels. Our results show the feasibility of gene therapy for targeting Klotho using CRISPR technology. Enhancing Klotho levels has a therapeutic potential for increasing cognition and treating age-associated neurodegenerative, demyelinating and other diseases, such as chronic kidney disease and cancer.
多种证据表明,抗衰老和认知增强蛋白 Klotho 促进神经元存活,增加抗氧化应激防御,并促进脱髓鞘轴突的髓鞘再生。因此,上调 Klotho 基因可能潜在缓解与年龄相关的神经退行性疾病(如阿尔茨海默病)和脱髓鞘疾病(如多发性硬化症)的症状和/或阻止其进展。在此,我们使用 CRISPR-dCas9 复合物研究针对 Klotho 启动子区域的单引导 RNA (sgRNA),以实现 Klotho 基因的高效转录激活。我们在 Klotho 启动子区域的 -1 到 -300bp 范围内测试了 sgRNA,并确定了两种可有效增强 Klotho 基因转录的 sgRNA。我们使用三种不同的系统检查 Klotho 基因的转录激活:萤火虫荧光素酶(FLuc)和纳米荧光素酶(NLuc)偶联报告系统、使用 CRISPR 基因组编辑在 Klotho 3'-UTR 中进行的 NLuc 基因敲入,以及两种内源性表达 Klotho 的人细胞系:神经元 SY5Y 细胞和肾 HK-2 细胞。这两种 sgRNA 均能在基因和蛋白水平上增强 Klotho 的表达。我们的结果表明,使用 CRISPR 技术靶向 Klotho 的基因治疗具有可行性。提高 Klotho 水平具有增加认知和治疗与年龄相关的神经退行性、脱髓鞘和其他疾病(如慢性肾病和癌症)的治疗潜力。