Literature DB >> 32081467

Identification of expanded repeats in NOTCH2NLC in neurodegenerative dementias.

Bin Jiao1, Lu Zhou2, Yafang Zhou3, Ling Weng1, Xinxin Liao3, Yun Tian3, Lina Guo2, Xixi Liu2, Zhenhua Yuan2, Xuewen Xiao2, Yaling Jiang2, Xin Wang2, Qijie Yang2, Chenping Li2, Yuan Zhu2, Lin Zhou3, Weiwei Zhang4, Junling Wang1, Yu Li2, Wenping Gu2, Jie Yang2, Jian Xia2, Qing Huang2, Jun Yin2, Jin Xue5, Ranhui Duan5, Beisha Tang1, Lu Shen6.   

Abstract

Recently, the (GGC)n repeat expansion in the NOTCH2NLC gene has been identified to be associated with neuronal intranuclear inclusion disease (NIID). Given the clinical overlap of dementia-dominant NIID with neurodegenerative dementia, we therefore hypothesized that the NOTCH2NLC repeat expansion might also contribute to these diseases. In the present study, repeat primed polymerase chain reaction (RP-PCR) and GC-rich PCR were conducted to detect the repeats of NOTCH2NLC in a cohort of 1004 patients with neurodegenerative dementias from mainland China. As a result, 4 sporadic patients were found to carry the NOTCH2NLC repeats expansion, totally accounting for 0.4% of all dementia individuals, and the accurate repeated sizes were 110, 133,120 and 76 respectively. Of 4 mutation carriers, three and one were clinically diagnosed Alzheimer's disease (AD) and frontotemporal dementia (FTD) respectively. In addition, 3 out of them revealed leukoencephalopathy in T2-Flair imaging. This study revealed that although rare, the NOTCH2NLC repeat expansions may be associated with AD or FTD-like phenotype as well as leukoencephalopathy.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Expanded repeats; NOTCH2NLC; Neurodegenerative dementia

Year:  2020        PMID: 32081467     DOI: 10.1016/j.neurobiolaging.2020.01.010

Source DB:  PubMed          Journal:  Neurobiol Aging        ISSN: 0197-4580            Impact factor:   4.673


  13 in total

1.  CGG repeat expansion in NOTCH2NLC causes mitochondrial dysfunction and progressive neurodegeneration in Drosophila model.

Authors:  Jiaxi Yu; Tongling Liufu; Yilei Zheng; Jin Xu; Lingchao Meng; Wei Zhang; Yun Yuan; Daojun Hong; Nicolas Charlet-Berguerand; Zhaoxia Wang; Jianwen Deng
Journal:  Proc Natl Acad Sci U S A       Date:  2022-10-03       Impact factor: 12.779

2.  GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy.

Authors:  Jiaxi Yu; Xing-Hua Luan; Meng Yu; Wei Zhang; He Lv; Li Cao; Lingchao Meng; Min Zhu; Binbin Zhou; Xiao-Rong Wu; Pidong Li; Qiang Gang; Jing Liu; Xin Shi; Wei Liang; Zhirong Jia; Sheng Yao; Yun Yuan; Jianwen Deng; Daojun Hong; Zhaoxia Wang
Journal:  Ann Clin Transl Neurol       Date:  2021-05-04       Impact factor: 4.511

3.  CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations.

Authors:  Masashi Ogasawara; Aritoshi Iida; Theerawat Kumutpongpanich; Ayami Ozaki; Yasushi Oya; Hirofumi Konishi; Akinori Nakamura; Ryuta Abe; Hiroshi Takai; Ritsuko Hanajima; Hiroshi Doi; Fumiaki Tanaka; Hisayoshi Nakamura; Ikuya Nonaka; Zhaoxia Wang; Shinichiro Hayashi; Satoru Noguchi; Ichizo Nishino
Journal:  Acta Neuropathol Commun       Date:  2020-11-25       Impact factor: 7.801

4.  Neuronal intranuclear inclusion disease mimicking acute cerebellitis: A case report.

Authors:  Jiao-Jiao Guo; Zi-Yi Wang; Meng Wang; Zong-Zhi Jiang; Xue-Fan Yu
Journal:  World J Clin Cases       Date:  2020-12-06       Impact factor: 1.337

5.  Natural selection at the RASGEF1C (GGC) repeat in human and divergent genotypes in late-onset neurocognitive disorder.

Authors:  Z Jafarian; S Khamse; H Afshar; H R Khorram Khorshid; A Delbari; M Ohadi
Journal:  Sci Rep       Date:  2021-09-28       Impact factor: 4.996

Review 6.  Cognitive Dysfunction in Repeat Expansion Diseases: A Review.

Authors:  Sizhe Zhang; Lu Shen; Bin Jiao
Journal:  Front Aging Neurosci       Date:  2022-04-11       Impact factor: 5.750

7.  Case report: Adult-onset neuronal intranuclear inclusion disease with an amyotrophic lateral sclerosis phenotype.

Authors:  Masako Fujita; Tatsuya Ueno; Yasuo Miki; Akira Arai; Hidekachi Kurotaki; Koichi Wakabayashi; Masahiko Tomiyama
Journal:  Front Neurosci       Date:  2022-08-10       Impact factor: 5.152

8.  The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3.

Authors:  Jiaxi Yu; Jianwen Deng; Xueyu Guo; Jingli Shan; Xinghua Luan; Li Cao; Juan Zhao; Meng Yu; Wei Zhang; He Lv; Zhiying Xie; LingChao Meng; Yiming Zheng; Yawen Zhao; Qiang Gang; Qingqing Wang; Jing Liu; Min Zhu; Binbin Zhou; Pidong Li; Yinzhe Liu; Yang Wang; Chuanzhu Yan; Daojun Hong; Yun Yuan; Zhaoxia Wang
Journal:  Brain       Date:  2021-07-28       Impact factor: 13.501

9.  Evolution of Human Brain Size-Associated NOTCH2NL Genes Proceeds toward Reduced Protein Levels.

Authors:  Gerrald A Lodewijk; Diana P Fernandes; Iraklis Vretzakis; Jeanne E Savage; Frank M J Jacobs
Journal:  Mol Biol Evol       Date:  2020-09-01       Impact factor: 16.240

10.  Therapeutic Development for CGG Repeat Expansion-Associated Neurodegeneration.

Authors:  Keqin Xu; Yujing Li; Emily G Allen; Peng Jin
Journal:  Front Cell Neurosci       Date:  2021-05-12       Impact factor: 5.505

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