• 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

患有 Smith-Magenis 缺失和 Potocki-Lupski 重复综合征的小鼠表现出相反的表型,表明基因剂量对液体消耗行为有影响。

Opposing phenotypes in mice with Smith-Magenis deletion and Potocki-Lupski duplication syndromes suggest gene dosage effects on fluid consumption behavior.

机构信息

Department of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, Tennessee, USA.

出版信息

Am J Med Genet A. 2012 Nov;158A(11):2807-14. doi: 10.1002/ajmg.a.35601. Epub 2012 Sep 18.

DOI:10.1002/ajmg.a.35601
PMID:22991245
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3477298/
Abstract

A quantitative long-term fluid consumption and fluid-licking assay was performed in two mouse models with either an ∼2 Mb genomic deletion, Df(11)17, or the reciprocal duplication copy number variation (CNV), Dp(11)17, analogous to the human genomic rearrangements causing either Smith-Magenis syndrome [SMS; OMIM #182290] or Potocki-Lupski syndrome [PTLS; OMIM #610883], respectively. Both mouse strains display distinct quantitative alterations in fluid consumption compared to their wild-type littermates; several of these changes are diametrically opposing between the two chromosome engineered mouse models. Mice with duplication versus deletion showed longer versus shorter intervals between visits to the waterspout, generated more versus less licks per visit and had higher versus lower variability in the number of licks per lick-burst as compared to their respective wild-type littermates. These findings suggest that copy number variation can affect long-term fluid consumption behavior in mice. Other behavioral differences were unique for either the duplication or deletion mutants; the deletion CNV resulted in increased variability of the licking rhythm, and the duplication CNV resulted in a significant slowing of the licking rhythm. Our findings document a readily quantitated complex behavioral response that can be directly and reciprocally influenced by a gene dosage effect.

摘要

我们在两种小鼠模型中进行了一项定量的长期液体消耗和舔舐实验,这两种模型分别携带约 2Mb 的基因组缺失(Df(11)17)或反向重复的拷贝数变异(CNV)(Dp(11)17),类似于导致史密斯-马根尼斯综合征(SMS;OMIM#182290)或波托基-卢普斯基综合征(PTLS;OMIM#610883)的人类基因组重排。与野生型同窝仔相比,这两种小鼠品系在液体消耗方面表现出明显的定量改变;在这两种经过基因工程改造的小鼠模型之间,有几个变化是截然相反的。与缺失相比,具有重复的小鼠在前往水嘴的间隔时间更长,每次访问的舔舐次数更多,每个舔舐爆发的舔舐次数的变异性更高,而与各自的野生型同窝仔相比。这些发现表明,拷贝数变异会影响小鼠的长期液体消耗行为。其他行为差异是重复或缺失突变体所特有的;缺失 CNV 导致舔舐节律的变异性增加,而重复 CNV 导致舔舐节律显著减慢。我们的研究结果记录了一种易于定量的复杂行为反应,它可以直接和相互地受到基因剂量效应的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aff2/3477298/b5e2ff75b09f/nihms394291f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aff2/3477298/9c5dd559c18a/nihms394291f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aff2/3477298/b5e2ff75b09f/nihms394291f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aff2/3477298/9c5dd559c18a/nihms394291f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aff2/3477298/b5e2ff75b09f/nihms394291f2.jpg

相似文献

1
Opposing phenotypes in mice with Smith-Magenis deletion and Potocki-Lupski duplication syndromes suggest gene dosage effects on fluid consumption behavior.患有 Smith-Magenis 缺失和 Potocki-Lupski 重复综合征的小鼠表现出相反的表型,表明基因剂量对液体消耗行为有影响。
Am J Med Genet A. 2012 Nov;158A(11):2807-14. doi: 10.1002/ajmg.a.35601. Epub 2012 Sep 18.
2
A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men.一个传递与代谢综合征相反特征的拷贝数变异(CNV),并在小鼠和人类中保护其免受饮食诱导的肥胖。
PLoS Genet. 2012;8(5):e1002713. doi: 10.1371/journal.pgen.1002713. Epub 2012 May 24.
3
Reciprocal deletion and duplication of 17p11.2-11.2: Korean patients with Smith-Magenis syndrome and Potocki-Lupski syndrome.17p11.2-11.2 相互缺失和重复:韩国史密斯-马根尼斯综合征和波托基-卢普斯基综合征患者。
J Korean Med Sci. 2012 Dec;27(12):1586-90. doi: 10.3346/jkms.2012.27.12.1586. Epub 2012 Dec 7.
4
Phenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse models.拷贝数变异的表型后果:来自 Smith-Magenis 和 Potocki-Lupski 综合征小鼠模型的见解。
PLoS Biol. 2010 Nov 23;8(11):e1000543. doi: 10.1371/journal.pbio.1000543.
5
Circadian abnormalities in mouse models of Smith-Magenis syndrome: evidence for involvement of RAI1.Smith-Magenis 综合征小鼠模型中的昼夜节律异常:RAI1 参与的证据。
Am J Med Genet A. 2013 Jul;161A(7):1561-8. doi: 10.1002/ajmg.a.35941. Epub 2013 May 23.
6
Inherited dup(17)(p11.2p11.2): expanding the phenotype of the Potocki-Lupski syndrome.遗传性重复(17)(p11.2p11.2):扩展波托茨基-卢普斯基综合征的表型
Am J Med Genet A. 2014 Feb;164A(2):500-4. doi: 10.1002/ajmg.a.36287. Epub 2013 Dec 5.
7
The behavioural phenotype of Potocki-Lupski syndrome: a cross-syndrome comparison.波托茨基-卢普斯基综合征的行为表型:跨综合征比较。
J Neurodev Disord. 2018 Jan 10;10(1):2. doi: 10.1186/s11689-017-9221-x.
8
Mouse models of genomic syndromes as tools for understanding the basis of complex traits: an example with the smith-magenis and the potocki-lupski syndromes.基因组综合征的小鼠模型作为理解复杂性状基础的工具:以 smith-magenis 和 potocki-lupski 综合征为例。
Curr Genomics. 2009 Jun;10(4):259-68. doi: 10.2174/138920209788488508.
9
Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndrome.与波托斯基-卢普斯基综合征相关的肾脏异常的关键遗传区间的定义。
Am J Med Genet A. 2012 Jul;158A(7):1579-88. doi: 10.1002/ajmg.a.35399. Epub 2012 May 25.
10
Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits.富养改善了基于脉络膜新生血管的自闭症样特征的动物模型的行为反应。
Hum Mol Genet. 2012 Jul 15;21(14):3083-96. doi: 10.1093/hmg/dds124. Epub 2012 Apr 5.

引用本文的文献

1
The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation.多种新生拷贝数变异(MdnCNV)现象具有胚胎期 DNA 突变特征和多位点致病性变异。
Genome Med. 2022 Oct 27;14(1):122. doi: 10.1186/s13073-022-01123-w.
2
Biology in balance: human diploid genome integrity, gene dosage, and genomic medicine.平衡的生物学:人类二倍体基因组完整性、基因剂量和基因组医学。
Trends Genet. 2022 Jun;38(6):554-571. doi: 10.1016/j.tig.2022.03.001. Epub 2022 Apr 18.
3
Prenatal Diagnosis of 17p11.2 Copy Number Abnormalities Associated With Smith-Magenis and Potocki-Lupski Syndromes in Fetuses.

本文引用的文献

1
A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men.一个传递与代谢综合征相反特征的拷贝数变异(CNV),并在小鼠和人类中保护其免受饮食诱导的肥胖。
PLoS Genet. 2012;8(5):e1002713. doi: 10.1371/journal.pgen.1002713. Epub 2012 May 24.
2
Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits.富养改善了基于脉络膜新生血管的自闭症样特征的动物模型的行为反应。
Hum Mol Genet. 2012 Jul 15;21(14):3083-96. doi: 10.1093/hmg/dds124. Epub 2012 Apr 5.
3
Consensus paper: pathological role of the cerebellum in autism.
胎儿中与史密斯-马吉尼斯综合征和波托基-卢普斯基综合征相关的17p11.2拷贝数异常的产前诊断
Front Genet. 2021 Dec 21;12:779237. doi: 10.3389/fgene.2021.779237. eCollection 2021.
4
2018 Victor A. McKusick Leadership Award: Molecular Mechanisms for Genomic and Chromosomal Rearrangements.2018年维克多·A·麦库西克领导力奖:基因组和染色体重排的分子机制
Am J Hum Genet. 2019 Mar 7;104(3):391-406. doi: 10.1016/j.ajhg.2018.12.018.
5
Lentiviral-mediated knock-down of GD3 synthase protects against MPTP-induced motor deficits and neurodegeneration.慢病毒介导的GD3合酶敲低可预防MPTP诱导的运动功能障碍和神经退行性变。
Neurosci Lett. 2019 Jan 23;692:53-63. doi: 10.1016/j.neulet.2018.10.038. Epub 2018 Nov 1.
6
Structural variation mutagenesis of the human genome: Impact on disease and evolution.人类基因组的结构变异诱变:对疾病和进化的影响。
Environ Mol Mutagen. 2015 Jun;56(5):419-36. doi: 10.1002/em.21943. Epub 2015 Apr 17.
7
The neuronal code(s) of the cerebellum.小脑的神经元编码(系统)。
J Neurosci. 2013 Nov 6;33(45):17603-9. doi: 10.1523/JNEUROSCI.2759-13.2013.
共识文件:小脑在自闭症中的病理作用。
Cerebellum. 2012 Sep;11(3):777-807. doi: 10.1007/s12311-012-0355-9.
4
Searching for Potocki-Lupski syndrome phenotype: a patient with language impairment and no autism.寻找波托基-卢普斯基综合征的表型:一名有语言障碍但无自闭症的患者。
Brain Dev. 2012 Sep;34(8):700-3. doi: 10.1016/j.braindev.2011.11.003. Epub 2011 Dec 16.
5
Comprehensive motor testing in Fmr1-KO mice exposes temporal defects in oromotor coordination.对Fmr1基因敲除小鼠进行的全面运动测试揭示了口面部运动协调方面的时间缺陷。
Behav Neurosci. 2011 Dec;125(6):962-9. doi: 10.1037/a0025920. Epub 2011 Oct 17.
6
Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.在自闭症中发现的 16p11.2 病变模型中存在剂量依赖性表型。
Proc Natl Acad Sci U S A. 2011 Oct 11;108(41):17076-81. doi: 10.1073/pnas.1114042108. Epub 2011 Oct 3.
7
Potocki-Lupski syndrome: a microduplication syndrome associated with oropharyngeal dysphagia and failure to thrive.波托茨基-卢普斯基综合征:一种与口咽吞咽困难和生长发育不良相关的微重复综合征。
J Pediatr. 2011 Apr;158(4):655-659.e2. doi: 10.1016/j.jpeds.2010.09.062. Epub 2010 Dec 17.
8
Phenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse models.拷贝数变异的表型后果:来自 Smith-Magenis 和 Potocki-Lupski 综合征小鼠模型的见解。
PLoS Biol. 2010 Nov 23;8(11):e1000543. doi: 10.1371/journal.pbio.1000543.
9
Cerebellar cortical output encodes temporal aspects of rhythmic licking movements and is necessary for normal licking frequency.小脑皮层输出编码节律性舔舐运动的时间方面,并且对于正常的舔舐频率是必要的。
Eur J Neurosci. 2010 Jul;32(1):41-52. doi: 10.1111/j.1460-9568.2010.07244.x. Epub 2010 Jun 28.
10
The clinical context of copy number variation in the human genome.人类基因组中拷贝数变异的临床背景。
Expert Rev Mol Med. 2010 Mar 9;12:e8. doi: 10.1017/S1462399410001390.