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通过抑制 Sup4h 的表达选择性降低突变 huntingtin 等位基因的表达对小鼠行为和寿命的影响。

Effects on murine behavior and lifespan of selectively decreasing expression of mutant huntingtin allele by supt4h knockdown.

机构信息

Institute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, Taiwan, Republic of China.

Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan, Republic of China.

出版信息

PLoS Genet. 2015 Mar 11;11(3):e1005043. doi: 10.1371/journal.pgen.1005043. eCollection 2015 Mar.

DOI:10.1371/journal.pgen.1005043
PMID:25760041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4356588/
Abstract

Production of protein containing lengthy stretches of polyglutamine encoded by multiple repeats of the trinucleotide CAG is a hallmark of Huntington's disease (HD) and of a variety of other inherited degenerative neurological and neuromuscular disorders. Earlier work has shown that interference with production of the transcription elongation protein SUPT4H results in decreased cellular capacity to transcribe mutant huntingtin gene (Htt) alleles containing long CAG expansions, but has little effect on expression of genes containing short CAG stretches. zQ175 and R6/2 are genetically engineered mouse strains whose genomes contain human HTT alleles that include greatly expanded CAG repeats and which are used as animal models for HD. Here we show that reduction of SUPT4H expression in brains of zQ175 mice by intracerebroventricular bolus injection of antisense 2'-O-methoxyethyl oligonucleotides (ASOs) directed against Supt4h, or in R6/2 mice by deletion of one copy of the Supt4h gene, results in a decrease in mRNA and protein encoded specifically by mutant Htt alleles. We further show that reduction of SUPT4H in mouse brains is associated with decreased HTT protein aggregation, and in R6/2 mice, also with prolonged lifespan and delay of the motor impairment that normally develops in these animals. Our findings support the view that targeting of SUPT4H function may be useful as a therapeutic countermeasure against HD.

摘要

由三核苷酸 CAG 多次重复编码的含有长段聚谷氨酰胺的蛋白质的产生是亨廷顿病(HD)和多种其他遗传性退行性神经和神经肌肉疾病的标志。早期的研究表明,干扰转录延伸蛋白 SUPT4H 的产生会导致细胞转录含有长 CAG 扩展的突变 huntingtin 基因(Htt)等位基因的能力下降,但对含有短 CAG 延伸的基因的表达几乎没有影响。zQ175 和 R6/2 是经过基因工程改造的小鼠品系,其基因组中含有人类 HTT 等位基因,这些等位基因包含大大扩展的 CAG 重复序列,可用作 HD 的动物模型。在这里,我们表明通过向 zQ175 小鼠的脑内脑室内推注针对 Supt4h 的反义 2'-O-甲氧基乙基寡核苷酸(ASO)或通过删除 Supt4h 基因的一个拷贝来减少 SUPT4H 的表达会导致突变 Htt 等位基因特异性的 mRNA 和蛋白质减少。我们进一步表明,减少小鼠脑中的 SUPT4H 与 HTT 蛋白聚集体减少有关,在 R6/2 小鼠中,还与寿命延长和这些动物通常发展的运动障碍延迟有关。我们的发现支持了这样一种观点,即靶向 SUPT4H 功能可能是一种有用的治疗对策,可用于对抗 HD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c4/4356588/fd95e3347559/pgen.1005043.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c4/4356588/4a73fc1d0bb9/pgen.1005043.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c4/4356588/202c6b759172/pgen.1005043.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c4/4356588/929e520441ac/pgen.1005043.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c4/4356588/7b524110063e/pgen.1005043.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c4/4356588/fd95e3347559/pgen.1005043.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c4/4356588/4a73fc1d0bb9/pgen.1005043.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c4/4356588/202c6b759172/pgen.1005043.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c4/4356588/929e520441ac/pgen.1005043.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c4/4356588/7b524110063e/pgen.1005043.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c4/4356588/fd95e3347559/pgen.1005043.g005.jpg

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