• 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

肌肉发育不全基因对小鼠下颌骨发育稳定性的影响。

Effects of the muscular dysgenesis gene on developmental stability in the mouse mandible.

作者信息

Atchley W R, Herring S W, Riska B, Plummer A A

出版信息

J Craniofac Genet Dev Biol. 1984;4(3):179-89.

PMID:6501560
Abstract

Muscular dysgenesis (mdg) is an autosomal recessive gene in mice affecting primarily the skeletal musculature. mdg/mdg mice exhibit developmental arrest of myogenesis and degenerative changes in all skeletal muscles. In addition, there are pronounced abnormalities in skeletal traits, including the shape of the skull and mandible. Herein, we examine the phenotypic consequences of a single mdg allele in the heterozygous condition (+/mdg) on the size, shape, and developmental stability in 14 osteometric traits from the mouse mandible. Developmental stability in the mandible is measured by fluctuating asymmetry in bilateral traits. There are no statistically significant differences in the size or shape of the mandible between +/+ and +/mdg mice. However, compared to +/+ mice, +/mdg individuals exhibit less developmental stability for several mandible traits. The more unstable traits include height at the mandibular notch, height at the incisive process, condyloid width, height and area of the coronoid process, and size of the tooth-bearing region. All of these latter traits are closely associated with areas of muscle attachment and/or the muscular dysgenesis phenotype, suggesting that the presence of a single mdg allele is sufficient to alter developmental pathways. Traits not showing significantly increased instability in +/mdg mice bear no clear relationship to either muscle attachment areas or to the mdg/mdg phenotype.

摘要

肌肉发育不全(mdg)是小鼠中的一种常染色体隐性基因,主要影响骨骼肌肉组织。mdg/mdg小鼠表现出肌生成的发育停滞以及所有骨骼肌的退行性变化。此外,骨骼特征存在明显异常,包括头骨和下颌骨的形状。在此,我们研究了杂合状态(+/mdg)下单个mdg等位基因对小鼠下颌骨14个骨测量性状的大小、形状和发育稳定性的表型影响。下颌骨的发育稳定性通过双侧性状的波动不对称性来衡量。+/+和+/mdg小鼠在下颌骨的大小或形状上没有统计学上的显著差异。然而,与+/+小鼠相比,+/mdg个体在几个下颌骨性状上表现出较低的发育稳定性。更不稳定的性状包括下颌切迹高度、切牙突高度、髁突宽度、冠突高度和面积以及含牙区大小。所有这些后述性状都与肌肉附着区域和/或肌肉发育不全表型密切相关,这表明单个mdg等位基因的存在足以改变发育途径。在+/mdg小鼠中未显示出明显增加的不稳定性的性状与肌肉附着区域或mdg/mdg表型均无明确关系。

相似文献

1
Effects of the muscular dysgenesis gene on developmental stability in the mouse mandible.肌肉发育不全基因对小鼠下颌骨发育稳定性的影响。
J Craniofac Genet Dev Biol. 1984;4(3):179-89.
2
Craniofacial development in the absence of muscle contraction.
J Craniofac Genet Dev Biol. 1982;1(4):341-57.
3
Elimination by necrosis, not apoptosis, of embryonic extraocular muscles in the muscular dysgenesis mutant of the mouse.在小鼠肌肉发育不全突变体中,胚胎眼外肌通过坏死而非凋亡被清除。
Cell Tissue Res. 2004 Feb;315(2):243-7. doi: 10.1007/s00441-003-0831-0. Epub 2003 Nov 14.
4
Restoration of dysgenic muscle contraction and calcium channel function by co-culture with normal spinal cord neurons.与正常脊髓神经元共培养恢复发育异常的肌肉收缩和钙通道功能。
Nature. 1987;330(6148):563-6. doi: 10.1038/330563a0.
5
Myotube driven myogenic recruitment of cells during in vitro myogenesis.在体外成肌过程中,肌管驱动细胞的肌源性募集。
Dev Dyn. 1995 Feb;202(2):126-36. doi: 10.1002/aja.1002020204.
6
Regulation of myogenesis in paralyzed muscles in the mouse mutants peroneal muscular atrophy and muscular dysgenesis.小鼠突变体腓骨肌萎缩症和肌肉发育不全中麻痹肌肉的肌生成调节
Dev Biol. 1993 Apr;156(2):529-36. doi: 10.1006/dbio.1993.1099.
7
Relationship of genotype and in vitro contractility in mdg/mdg in equilibrium +/+ "mosaic" myotubes.平衡状态下mdg/mdg与+/+“嵌合”肌管中基因型与体外收缩性的关系。
Muscle Nerve. 1984 Mar-Apr;7(3):194-203. doi: 10.1002/mus.880070303.
8
Early effects in vitro of the muscular dysgenesis mutation on nervous tissue in the mouse.肌肉发育不全突变对小鼠神经组织的早期体外影响。
Muscle Nerve. 1984 Mar-Apr;7(3):179-93. doi: 10.1002/mus.880070302.
9
A quantitative genetic analysis of localized morphology in mandibles of inbred mice using finite element scaling analysis.使用有限元缩放分析对近交系小鼠下颌骨局部形态进行的数量遗传学分析。
J Craniofac Genet Dev Biol. 1991 Jul-Sep;11(3):122-37.
10
Selection in a cycling population: differential response among skeletal traits.骑行人群中的选择:骨骼特征的差异反应。
Evolution. 2006 Sep;60(9):1925-35.

引用本文的文献

1
Distinct transcriptomic changes in E14.5 mouse skeletal muscle lacking RYR1 or Cav1.1 converge at E18.5.E14.5 缺乏 RYR1 或 Cav1.1 的小鼠骨骼肌肉的转录组变化在 E18.5 时趋于一致。
PLoS One. 2018 Mar 15;13(3):e0194428. doi: 10.1371/journal.pone.0194428. eCollection 2018.
2
Genetics of mandible form in the mouse.小鼠下颌骨形态的遗传学
Genetics. 1985 Nov;111(3):555-77. doi: 10.1093/genetics/111.3.555.