Courtship and distress ultrasonic vocalizations are altered in a mouse model of Angelman syndrome.

IF 3.6 2区 医学 Q1 CLINICAL NEUROLOGY
Caleigh D Guoynes, Grace Pavalko, Michael S Sidorov
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Abstract

BACKGROUND: Angelman syndrome (AS) is a single-gene neurodevelopmental disorder caused by loss of function of the maternal copy of the UBE3A gene. Nearly all individuals with AS lack speech, resulting in major impacts on daily life for patients and caregivers. To evaluate new therapies for AS, it is crucial to have a mouse model that characterizes meaningful clinical features. Vocalizations are used in many contexts in mice, including pup retrieval, social interactions, courtship, and distress. Previous work in the Ube3am−/p+ mouse model of AS found abnormalities in the number of ultrasonic vocalizations (USVs) mice produced during pup isolation and same-sex social interactions. Here, we evaluated Ube3am−/p+ vocalizations during courtship and distress. Quantifying USVs in these contexts enables comparison of USVs in social (courtship) and non-social (distress) settings. In addition, we assessed the utility of incorporating USV testing into existing Ube3am−/p+ mouse behavioral assessments used to evaluate potential AS treatments. METHODS: We used multiple behavioral paradigms to evaluate courtship vocalizations and tail suspension tests to evaluate distress vocalizations in adult wild-type (WT) and Ube3am−/p+ littermates, and quantified USV properties using the program DeepSqueak. A subset of mice also performed an established Ube3am−/p+ behavioral battery that included rotarod, open field, marble burying, and nest building. We used principal component analysis to evaluate the value of USV testing in this cohort in the context of other behaviors. RESULTS: In both social courtship and nonsocial distress behavioral paradigms, Ube3am−/p+ mice made fewer USVs compared to WT mice. Spectral properties of USVs were abnormal in Ube3am−/p+ mice on courtship tests but mostly typical on distress tests. Including USVs in the Ube3am−/p+ mouse behavior battery increased the distance between Ube3am−/p+ and WT clusters in principal component space. CONCLUSIONS: Ube3am−/p+ mice have disrupted USV production in social and nonsocial contexts. Spectral properties of USVs are most impacted in the social courtship context. Adding USVs to the Ube3am−/p+ behavior battery may improve sensitivity to detect group differences and changes in communication.

在天使症候群的小鼠模型中,求偶和痛苦的超声波发声被改变。
背景:Angelman综合征(AS)是一种单基因神经发育障碍,由母体UBE3A基因拷贝的功能丧失引起。几乎所有的AS患者都缺乏语言能力,这对患者和护理人员的日常生活产生了重大影响。为了评估AS的新疗法,建立具有临床特征的小鼠模型至关重要。发声在老鼠的许多情况下都有应用,包括找回幼崽、社会互动、求爱和痛苦。先前在Ube3am - /p+ AS小鼠模型中发现,在幼鼠隔离和同性社会互动期间,小鼠产生的超声波发声(usv)数量异常。在这里,我们评估了Ube3am−/p+在求偶和痛苦期间的发声。在这些情况下量化usv可以比较社交(求爱)和非社交(痛苦)环境下的usv。此外,我们评估了将USV测试纳入现有Ube3am - /p+小鼠行为评估的效用,用于评估潜在的AS治疗。方法:我们使用多种行为范式来评估求偶发声,并通过尾悬测试来评估成年野生型(WT)和Ube3am−/p+幼崽的痛苦发声,并使用DeepSqueak程序量化USV特性。一组小鼠还进行了建立的Ube3am−/p+行为电池,包括旋转杆、开阔场地、大理石掩埋和筑巢。我们使用主成分分析来评估在其他行为背景下USV测试在该队列中的价值。结果:在社会求爱和非社会痛苦行为范式中,Ube3am−/p+小鼠的usv比WT小鼠少。在求偶试验中,Ube3am−/p+小鼠usv的光谱特性是异常的,而在痛苦试验中则是典型的。在Ube3am−/p+小鼠行为电池中加入usv增加了Ube3am−/p+与WT簇在主成分空间中的距离。结论:Ube3am−/p+小鼠在社会和非社会环境中破坏了USV的产生。usv的频谱特性在社会求爱环境中受到的影响最大。将usv添加到Ube3am−/p+行为电池中可以提高灵敏度,以检测群体差异和通信变化。
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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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