• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

高通量分析叫声揭示 Fmr1 突变体幼鼠中性别特异性的变化。

High-throughput analysis of vocalizations reveals sex-specific changes in Fmr1 mutant pups.

机构信息

Department of Psychology and Neuroscience, Baylor University, Waco, Texas.

Institute of Biomedical Studies, Baylor University, Waco, Texas.

出版信息

Genes Brain Behav. 2020 Feb;19(2):e12611. doi: 10.1111/gbb.12611. Epub 2019 Nov 1.

DOI:10.1111/gbb.12611
PMID:31587487
Abstract

There have been several reports that individuals with Fragile X syndrome (FXS) and animal models of FXS have communication deficits. The present study utilized two different call classification taxonomies to examine the sex-specificity of ultrasonic vocalization (USV) production on postnatal day (PD8) in the FVB strain of Fmr1 knockout (KO) mice. One classification protocol requires the investigator to score each call by hand, while the other protocol uses an automated algorithm. Results using the hand-scoring protocol indicated that male Fmr1 KO mice exhibited longer calls (P = .03) than wild types on PD8. Male KOs also produced fewer complex, composite, downward, short and two-syllable call-types, as well as more frequency steps and chevron call-types. Female heterozygotes exhibited no significant changes in acoustic or temporal aspects of calls, yet showed significant changes in call-type production proportions across two different classification taxonomies (P < .001). They exhibited increased production of harmonic and frequency steps calls, as well as fewer chevron, downward and short calls. According to the second high-throughput analysis, female heterozygotes produced significantly fewer single-type and more multiple-type syllables, unlike male KOs that showed no changes in these aspects of syllable production. Finally, we correlated both scoring methods and found a high level of correlation between the two methods. These results contribute further knowledge of sex differences in USV calling behavior for Fmr1 heterozygote and KO mice and provide a foundation for the use of high-throughput analysis of neonatal USVs.

摘要

已有多项研究报告指出脆性 X 综合征(FXS)患者和 FXS 动物模型存在沟通障碍。本研究采用两种不同的叫声分类法,以研究 Fmr1 敲除(KO)小鼠在产后第 8 天(PD8)时,雄性和雌性 Fmr1 敲除(KO)小鼠超声发声(USV)的产生是否存在性别特异性。一种分类方案要求研究人员手动为每个叫声打分,而另一种方案则使用自动算法。使用手动评分方案的结果表明,雄性 Fmr1 KO 小鼠在 PD8 时的叫声持续时间更长(P =.03)。雄性 KO 还产生了较少的复杂、复合、向下、短和双音节叫声类型,以及更多的频率步和人字形叫声类型。雌性杂合子在叫声的声学或时间方面没有表现出显著变化,但在两种不同的分类分类法中,叫声类型的产生比例发生了显著变化(P <.001)。它们表现出更多的谐波和频率步叫声,以及更少的人字形、向下和短叫声。根据第二种高通量分析,雌性杂合子产生的单音节和多音节的数量明显减少,而雄性 KO 则在这些音节产生方面没有变化。最后,我们对两种评分方法进行了相关性分析,发现两种方法之间具有高度相关性。这些结果进一步揭示了 Fmr1 杂合子和 KO 小鼠在 USV 叫声行为上的性别差异,并为新生儿 USV 的高通量分析提供了基础。

相似文献

1
High-throughput analysis of vocalizations reveals sex-specific changes in Fmr1 mutant pups.高通量分析叫声揭示 Fmr1 突变体幼鼠中性别特异性的变化。
Genes Brain Behav. 2020 Feb;19(2):e12611. doi: 10.1111/gbb.12611. Epub 2019 Nov 1.
2
Temporal and spectral differences in the ultrasonic vocalizations of fragile X knock out mice during postnatal development.脆性X基因敲除小鼠出生后发育过程中超声发声的时间和频谱差异。
Behav Brain Res. 2014 Feb 1;259:119-30. doi: 10.1016/j.bbr.2013.10.049. Epub 2013 Nov 7.
3
Reversal of ultrasonic vocalization deficits in a mouse model of Fragile X Syndrome with minocycline treatment or genetic reduction of MMP-9.使用米诺环素治疗或降低 MMP-9 基因表达可逆转脆性 X 综合征小鼠模型的超声发声缺陷。
Behav Brain Res. 2019 Oct 17;372:112068. doi: 10.1016/j.bbr.2019.112068. Epub 2019 Jul 2.
4
Sex-specific modulation of early life vocalization and cognition by Fmr1 gene dosage in a mouse model of Fragile X Syndrome.脆性 X 综合征小鼠模型中 Fmr1 基因剂量对早期发声和认知的性别特异性调节。
Biol Sex Differ. 2024 Feb 21;15(1):18. doi: 10.1186/s13293-024-00594-3.
5
Spectral and temporal properties of calls reveal deficits in ultrasonic vocalizations of adult Fmr1 knockout mice.叫声的频谱和时间特性揭示了成年Fmr1基因敲除小鼠超声发声的缺陷。
Behav Brain Res. 2017 Aug 14;332:50-58. doi: 10.1016/j.bbr.2017.05.052. Epub 2017 May 26.
6
Comprehensive analysis of ultrasonic vocalizations in a mouse model of fragile X syndrome reveals limited, call type specific deficits.全面分析脆性 X 综合征小鼠模型的超声发声,揭示了有限的、特定于叫声类型的缺陷。
PLoS One. 2012;7(9):e44816. doi: 10.1371/journal.pone.0044816. Epub 2012 Sep 11.
7
Characterization of ultrasonic vocalizations of Fragile X mice.脆性X小鼠超声发声的特征描述。
Behav Brain Res. 2016 Sep 1;310:76-83. doi: 10.1016/j.bbr.2016.04.016. Epub 2016 Apr 30.
8
Sex-specific and genotype-specific differences in vocalization development in FMR1 knockout mice.脆性X智力低下基因1敲除小鼠发声发育中的性别特异性和基因型特异性差异。
Neuroreport. 2016 Dec 14;27(18):1331-1335. doi: 10.1097/WNR.0000000000000701.
9
Minocycline treatment reverses ultrasonic vocalization production deficit in a mouse model of Fragile X Syndrome.米诺环素治疗可逆转脆性 X 综合征小鼠模型的超声发声产生缺陷。
Brain Res. 2012 Feb 23;1439:7-14. doi: 10.1016/j.brainres.2011.12.041. Epub 2011 Dec 31.
10
Multiple Early-Life Seizures Alters Neonatal Communicative Behavior in Fmr1 Knockout Mice.多次早期癫痫发作改变 Fmr1 敲除小鼠的新生期交流行为。
Dev Neurosci. 2022;44(6):478-486. doi: 10.1159/000524898. Epub 2022 May 5.

引用本文的文献

1
Distinct early development trajectories in Nf1 and Tsc2 mouse models of autism.自闭症的Nf1和Tsc2小鼠模型中不同的早期发育轨迹。
J Neurodev Disord. 2025 Jul 26;17(1):42. doi: 10.1186/s11689-025-09624-6.
2
A meta-analysis of sex differences in neonatal rodent ultrasonic vocalizations and the implication for the preclinical maternal immune activation model.新生啮齿动物超声发声性别差异的荟萃分析及其对临床前母体免疫激活模型的启示。
Biol Sex Differ. 2025 Jan 25;16(1):4. doi: 10.1186/s13293-025-00685-9.
3
A Two-Hit Approach Inducing Flurothyl Seizures in Fmr1 Knockout Mice Impacts Anxiety and Repetitive Behaviors.
一种在Fmr1基因敲除小鼠中诱发氟烷惊厥的双打击方法影响焦虑和重复行为。
Brain Sci. 2024 Aug 31;14(9):892. doi: 10.3390/brainsci14090892.
4
Distributed X chromosome inactivation in brain circuitry is associated with X-linked disease penetrance of behavior.脑回路中的分布式 X 染色体失活与行为相关的 X 连锁疾病外显率有关。
Cell Rep. 2024 Apr 23;43(4):114068. doi: 10.1016/j.celrep.2024.114068. Epub 2024 Apr 12.
5
Sex-specific modulation of early life vocalization and cognition by Fmr1 gene dosage in a mouse model of Fragile X Syndrome.脆性 X 综合征小鼠模型中 Fmr1 基因剂量对早期发声和认知的性别特异性调节。
Biol Sex Differ. 2024 Feb 21;15(1):18. doi: 10.1186/s13293-024-00594-3.
6
Temporal dynamics of isolation calls emitted by pups in environmental and genetic mouse models of autism spectrum disorder.自闭症谱系障碍环境和基因小鼠模型中幼崽发出的隔离叫声的时间动态。
Front Neurosci. 2023 Oct 23;17:1274039. doi: 10.3389/fnins.2023.1274039. eCollection 2023.
7
Prenatal SAMe Treatment Changes via Epigenetic Mechanism/s USVs in Young Mice and Hippocampal Monoamines Turnover at Adulthood in a Mouse Model of Social Hierarchy and Depression.产前 SAMe 治疗通过表观遗传机制改变幼鼠的 USVs,并在社会等级和抑郁小鼠模型中改变成年海马单胺类递质的代谢。
Int J Mol Sci. 2023 Jun 27;24(13):10721. doi: 10.3390/ijms241310721.
8
Fragile X Messenger Ribonucleoprotein 1 (FMR1), a novel inhibitor of osteoblast/osteocyte differentiation, regulates bone formation, mass, and strength in young and aged male and female mice.脆性X信使核糖核蛋白1(FMR1)是一种新型的成骨细胞/骨细胞分化抑制剂,可调节年轻和老年雄性及雌性小鼠的骨形成、骨量和骨强度。
Bone Res. 2023 May 17;11(1):25. doi: 10.1038/s41413-023-00256-x.
9
Assessment of the effects of sex, age, and rearing condition on ultrasonic vocalizations elicited by pups during the maternal potentiation paradigm in C57BL/6J mice.评估性别、年龄和饲养条件对 C57BL/6J 小鼠母性增强范式中幼崽诱发的超声发声的影响。
Dev Psychobiol. 2022 Dec;64(8):e22341. doi: 10.1002/dev.22341.
10
Long-term behavioral effects of prenatal stress in the Fmr1-knock-out mouse model for fragile X syndrome.脆性X综合征Fmr1基因敲除小鼠模型中产前应激的长期行为影响。
Front Cell Neurosci. 2022 Oct 27;16:917183. doi: 10.3389/fncel.2022.917183. eCollection 2022.