Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders

Yun Tian(Central South University), Junling Wang(Central South University), Wen Huang(Central South University), Sheng Zeng(Central South University), Bin Jiao(Central South University), Zhen Liu(Central South University), Chen Zhao(Central South University), Yujing Li(Emory University), Ying Wang(Central South University), Haoxuan Min(Bioscience (China)), Xuejing Wang(First Affiliated Hospital of Zhengzhou University), Yong You(First Affiliated Hospital of University of South China), Ruxu Zhang(Central South University), Xiaoyu Chen(Central South University), Fang Yi(Central South University), Yafang Zhou(Central South University), Hongyu Long(Central South University), Chaojun Zhou(Central South University), Xuan Hou(Central South University), Junpu Wang(Central South University), Bin Xie(Central South University), Fan Liang(Bioscience (China)), Zhuanyi Yang(Central South University), Qiying Sun(Central South University), Emily G. Allen(Emory University), Andrew M. Shafik(Emory University), Ha Eun Kong(Emory University), Jifeng Guo(Central South University), Xinxiang Yan(Central South University), Zhengmao Hu(Central South University), Kun Xia(Central South University), Hong Jiang(Central South University), Hongwei Xu(Central South University), Ranhui Duan(Central South University), Peng Jin(Emory University), Beisha Tang(Central South University), Lu Shen(Central South University)
The American Journal of Human Genetics
June 6, 2019
Cited by 323Open Access
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Abstract

Neuronal intranuclear inclusion disease (NIID) is a slowly progressing neurodegenerative disease characterized by eosinophilic intranuclear inclusions in the nervous system and multiple visceral organs. The clinical manifestation of NIID varies widely, and both familial and sporadic cases have been reported. Here we have performed genetic linkage analysis and mapped the disease locus to 1p13.3-q23.1; however, whole-exome sequencing revealed no potential disease-causing mutations. We then performed long-read genome sequencing and identified a large GGC repeat expansion within human-specific NOTCH2NLC. Expanded GGC repeats as the cause of NIID was further confirmed in an additional three NIID-affected families as well as five sporadic NIID-affected case subjects. Moreover, given the clinical heterogeneity of NIID, we examined the size of the GGC repeat among 456 families with a variety of neurological conditions with the known pathogenic genes excluded. Surprisingly, GGC repeat expansion was observed in two Alzheimer disease (AD)-affected families and three parkinsonism-affected families, implicating that the GGC repeat expansions in NOTCH2NLC could also contribute to the pathogenesis of both AD and PD. Therefore, we suggest defining a term NIID-related disorders (NIIDRD), which will include NIID and other related neurodegenerative diseases caused by the expanded GGC repeat within human-specific NOTCH2NLC.


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