异染色质
失智症
肌萎缩侧索硬化
C9orf72
生物
细胞生物学
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基因表达
分子生物学
三核苷酸重复扩增
遗传学
染色体
痴呆
基因
病理
肽序列
医学
疾病
等位基因
作者
Yong‐Jie Zhang,Lin Guo,Patrick Gonzales,Tania F. Gendron,Yanwei Wu,Karen Jansen‐West,Aliesha D. O’Raw,Sarah Pickles,Mercedes Prudencio,Yari Carlomagno,Mariam A. Gachechiladze,Connor Ludwig,Ruilin Tian,Jeannie Chew,Michael DeTure,Wen-Lang Lin,Jimei Tong,Lillian M. Daughrity,Mei Yue,Yuping Song
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2019-02-15
卷期号:363 (6428)
被引量:213
标识
DOI:10.1126/science.aav2606
摘要
How dipeptide repeats cause pathology A repeat expansion in the chromosome 9 open reading frame 72 ( C9orf72 ) gene is the most common known cause of two neurodegenerative diseases: frontotemporal dementia and amyotrophic lateral sclerosis. This expansion leads to the abnormal production of proteins of repeating dipeptides, but their contribution to disease pathogenesis remains unclear. Zhang et al. engineered a mouse model to study the consequences of one of these dipeptides—prolinearginine dipeptide repeat protein, poly(PR)—in the brain. They found that poly(PR) caused neuron loss as well as motor and memory impairments. These detrimental effects resulted from poly(PR)-induced perturbation of heterochromatin function, a tightly packed form of DNA that represses gene expression. Science , this issue p. eaav2606
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