Shared and specific signatures of locomotor ataxia in mutant mice

Author:

Machado Ana S1,Marques Hugo G1ORCID,Duarte Diogo F1,Darmohray Dana M1,Carey Megan R1ORCID

Affiliation:

1. Champalimaud Neuroscience Program, Champalimaud Center for the Unknown, Lisbon, Portugal

Abstract

Several spontaneous mouse mutants with deficits in motor coordination and associated cerebellar neuropathology have been described. Intriguingly, both visible gait alterations and neuroanatomical abnormalities throughout the brain differ across mutants. We previously used the LocoMouse system to quantify specific deficits in locomotor coordination in mildly ataxic Purkinje cell degeneration mice (pcd; Machado et al., 2015). Here, we analyze the locomotor behavior of severely ataxic reeler mutants and compare and contrast it with that of pcd. Despite clearly visible gait differences, direct comparison of locomotor kinematics and linear discriminant analysis reveal a surprisingly similar pattern of impairments in multijoint, interlimb, and whole-body coordination in the two mutants. These findings capture both shared and specific signatures of gait ataxia and provide a quantitative foundation for mapping specific locomotor impairments onto distinct neuropathologies in mice.

Funder

H2020 European Research Council

Howard Hughes Medical Institute

Fundação para a Ciência e a Tecnologia

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference62 articles.

1. Toward a science of computational ethology;Anderson;Neuron,2014

2. The cerebellum and control of rhythmical movements;Arshavsky;Trends in Neurosciences,1983

3. Cerebellar ataxia: abnormal control of interaction torques across multiple joints;Bastian;Journal of Neurophysiology,1996

4. lme Linear mixed-effects models using Eigen and S4;Bates,2013

5. The need for speed in rodent locomotion analyses;Batka;The Anatomical Record,2014

Cited by 23 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3