• 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

全基因组连锁扫描寻找抗肌肉疲劳的基因

Genome-wide linkage scan for resistance to muscle fatigue.

机构信息

Department of Biomedical Kinesiology, Research Center for Exercise and Health, Faculty of Kinesiology and Rehabilitation Sciences, Katholieke Universiteit Leuven, Leuven, Belgium.

出版信息

Scand J Med Sci Sports. 2011 Aug;21(4):580-8. doi: 10.1111/j.1600-0838.2009.01082.x. Epub 2010 Mar 10.

DOI:10.1111/j.1600-0838.2009.01082.x
PMID:20459472
Abstract

Repeated, intense use of muscles leads to a decline in performance known as muscle fatigue. Resistance to muscle fatigue depends on age, sex, muscle fiber type, activation by the nervous system and training. Heritability of muscle strength phenotypes ranges between 31% and 78%, although little is known about heritability of muscle fatigue. A first aim of this study was to estimate the heritability for fatigue resistance after a short bout of intense exercise of the knee musculature. The main purpose was to identify chromosomal regions linked to muscle fatigue applying genome-wide linkage analyses. A selection of 283 informative male siblings (17-36 years old), belonging to 105 families, was used to conduct a genome-wide SNP-based multipoint linkage analysis. Heritabilities for resistance to muscle fatigue ranged from 21% to 54%. The strongest linkage signal was found at 19q13.11 (LOD=2.158; P<0.0001) and at 1q32.1 (LOD=2.142; P<0.0001) for resistance to fatigue of the knee flexors; however, no marker reached genome-wide significance. Several other regions with LOD>1.5 were found (1p31.3, 3q29, 8p22, 11q25 and 19q12). When replicated in an independent sample, these results warrant further fine mapping studies aiming to detect genes that underlie variation in muscle fatigue.

摘要

肌肉的重复、高强度使用会导致肌肉疲劳,表现为运动能力下降。肌肉疲劳的抵抗力取决于年龄、性别、肌肉纤维类型、神经系统的激活和训练。肌肉力量表型的遗传率在 31%到 78%之间,尽管肌肉疲劳的遗传率知之甚少。本研究的第一个目的是估计膝关节肌肉短暂剧烈运动后疲劳抵抗的遗传率。主要目的是应用全基因组连锁分析来确定与肌肉疲劳相关的染色体区域。选择了 105 个家庭的 283 名有信息的男性同胞(17-36 岁)进行全基因组 SNP 多点连锁分析。肌肉疲劳抵抗力的遗传率范围为 21%至 54%。在股四头肌疲劳抵抗方面,最强的连锁信号位于 19q13.11(LOD=2.158;P<0.0001)和 1q32.1(LOD=2.142;P<0.0001),但没有一个标记达到全基因组显著水平。还发现了其他几个 LOD>1.5 的区域(1p31.3、3q29、8p22、11q25 和 19q12)。在独立样本中复制这些结果后,需要进一步进行精细定位研究,以检测导致肌肉疲劳变异的基因。

相似文献

1
Genome-wide linkage scan for resistance to muscle fatigue.全基因组连锁扫描寻找抗肌肉疲劳的基因
Scand J Med Sci Sports. 2011 Aug;21(4):580-8. doi: 10.1111/j.1600-0838.2009.01082.x. Epub 2010 Mar 10.
2
Genome-wide linkage scan for maximum and length-dependent knee muscle strength in young men: significant evidence for linkage at chromosome 14q24.3.针对年轻男性最大及长度依赖性膝部肌肉力量的全基因组连锁扫描:14号染色体q24.3区域存在连锁的显著证据。
J Med Genet. 2008 May;45(5):275-83. doi: 10.1136/jmg.2007.055277. Epub 2008 Jan 4.
3
Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies.通过全基因组连锁研究及后续关联研究,证明维生素D受体基因与特发性身材矮小有关。
Hum Mol Genet. 2006 Sep 15;15(18):2772-83. doi: 10.1093/hmg/ddl218. Epub 2006 Aug 11.
4
Quantitative trait loci for human muscle strength: linkage analysis of myostatin pathway genes.人类肌肉力量的数量性状基因座:肌肉生长抑制素通路基因的连锁分析
Physiol Genomics. 2005 Aug 11;22(3):390-7. doi: 10.1152/physiolgenomics.00010.2005. Epub 2005 May 24.
5
Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects.对患有注意力缺陷多动障碍的患病同胞对的阅读能力进行全基因组扫描:独特和共享的遗传效应。
Mol Psychiatry. 2004 May;9(5):485-93. doi: 10.1038/sj.mp.4001450.
6
Genome-wide linkage scan for contraction velocity characteristics of knee musculature in the Leuven Genes for Muscular Strength Study.鲁汶肌肉力量研究中膝关节肌肉收缩速度特征的全基因组连锁扫描。
Physiol Genomics. 2008 Sep 17;35(1):36-44. doi: 10.1152/physiolgenomics.90252.2008. Epub 2008 Aug 5.
7
Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study.在胰岛素抵抗动脉粥样硬化研究(IRAS)家族研究中,对与肥胖表型相关的17号染色体区域进行基因定位。
Int J Obes (Lond). 2006 Sep;30(9):1433-41. doi: 10.1038/sj.ijo.0803298. Epub 2006 Mar 7.
8
A genome-wide scan in affected sibling pairs with idiopathic recurrent miscarriage suggests genetic linkage.一项针对不明原因复发性流产的受累同胞对的全基因组扫描提示存在遗传连锁。
Mol Hum Reprod. 2011 Jun;17(6):379-85. doi: 10.1093/molehr/gar003. Epub 2011 Jan 20.
9
Linkage and association analyses of microsatellites and single-nucleotide polymorphisms in nuclear families.连锁与关联分析核家庭中的微卫星和单核苷酸多态性。
BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S25. doi: 10.1186/1471-2156-6-S1-S25.
10
Assessment of muscle fatigue during biking.骑行过程中肌肉疲劳的评估。
IEEE Trans Neural Syst Rehabil Eng. 2003 Mar;11(1):17-23. doi: 10.1109/TNSRE.2003.810425.

引用本文的文献

1
Endocrine crosstalk between muscle and bone.肌肉和骨骼之间的内分泌串扰。
Curr Osteoporos Rep. 2014 Jun;12(2):135-41. doi: 10.1007/s11914-014-0209-0.
2
Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family.对一个大型多代家族的心血管疾病生物标志物进行全基因组连锁分析。
PLoS One. 2013 Aug 2;8(8):e71779. doi: 10.1371/journal.pone.0071779. Print 2013.
3
Identification and prioritization of NUAK1 and PPP1CC as positional candidate loci for skeletal muscle strength phenotypes.鉴定和优先考虑 NUAK1 和 PPP1CC 作为骨骼肌力量表型的位置候选基因。
Physiol Genomics. 2011 Sep 8;43(17):981-92. doi: 10.1152/physiolgenomics.00200.2010. Epub 2011 Jul 12.
4
Comprehensive fine mapping of chr12q12-14 and follow-up replication identify activin receptor 1B (ACVR1B) as a muscle strength gene.全面精细定位 chr12q12-14,并进行后续复制,确定激活素受体 1B(ACVR1B)为肌肉力量基因。
Eur J Hum Genet. 2011 Feb;19(2):208-15. doi: 10.1038/ejhg.2010.173. Epub 2010 Nov 10.