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利用BXD重组近交系小鼠研究运动协调性,以模拟发育性协调障碍的遗传基础。

Investigating Motor Coordination Using BXD Recombinant Inbred Mice to Model the Genetic Underpinnings of Developmental Coordination Disorder.

作者信息

Rajan Jeffy Rajan Soundara, Gill Kamaldeep, Chow Eric, Ashbrook David G, Williams Robert W, Zwicker Jill G, Goldowitz Daniel

机构信息

Department of Medical Genetics, University of British Columbia, Vancouver, Canada.

Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, Canada.

出版信息

Genes Brain Behav. 2025 Apr;24(2):e70014. doi: 10.1111/gbb.70014.

Abstract

The fundamental skills for motor coordination and motor control emerge through development. Neurodevelopmental disorders such as developmental coordination disorder (DCD) lead to impaired acquisition of motor skills. This study investigated motor behaviors that reflect the core symptoms of human DCD through the use of BXD recombinant inbred strains of mice that are known to have divergent phenotypes in many behavioral traits, including motor activity. We sought to correlate behavior in basic motor control tasks with the known genotypes of these reference populations of mice using quantitative trait locus (QTL) mapping. We used 12 BXD strains with an average of 16 mice per group to assess the onset of reflexes during the early neonatal stage of life and differences in motor coordination using the tests for open field, rotarod, and gait behaviors during the adolescent/young adulthood period. Results indicated significant variability between strains in when neonatal reflexes appeared and significant strain differences for all measures of motor coordination. Five strains (BXD15, BXD27, BXD28, BXD75, BXD86) struggled with sensorimotor coordination as seen in gait analysis, rotarod, and open field, similar to human presentation of DCD. We identified three significant quantitative trait loci for gait on proximal Chr 3, Chr 4, and distal Chr 6. Based on expression, function, and polymorphism within the mapped QTL intervals, seven candidate genes (Gpr63, Spata5, Trpc3, Cntn6, Chl1, Grm7, Ogg1) emerged. This study offers new insights into mouse motor behavior, which promises to be a first murine model to explore the genetics and neural correlates of DCD.

摘要

运动协调和运动控制的基本技能是在发育过程中逐渐形成的。诸如发育性协调障碍(DCD)等神经发育障碍会导致运动技能的获得受损。本研究通过使用BXD重组近交系小鼠来探究反映人类DCD核心症状的运动行为,已知这些小鼠在包括运动活动在内的许多行为特征方面具有不同的表型。我们试图通过数量性状基因座(QTL)定位,将基本运动控制任务中的行为与这些小鼠参考群体的已知基因型相关联。我们使用了12个BXD品系,每组平均16只小鼠,以评估生命早期新生儿阶段反射的出现情况,并在青春期/成年早期使用旷场试验、转棒试验和步态行为测试来评估运动协调性的差异。结果表明,各品系在新生儿反射出现的时间上存在显著差异,并且在所有运动协调性测量指标上也存在显著的品系差异。五个品系(BXD15、BXD27、BXD28、BXD75、BXD86)在步态分析、转棒试验和旷场试验中表现出感觉运动协调困难,类似于人类DCD的表现。我们在近端第3号染色体、第4号染色体和远端第6号染色体上确定了三个与步态相关的重要数量性状基因座。基于定位的QTL区间内的表达、功能和多态性,出现了七个候选基因(Gpr63、Spata5、Trpc3、Cntn6、Chl1、Grm7、Ogg1)。本研究为小鼠运动行为提供了新的见解,有望成为探索DCD遗传学和神经相关性的首个小鼠模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8b7/11898013/b35231755a60/GBB-24-e70014-g001.jpg

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