• 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

基于不同物种内和物种间MSTN基因完整编码区的生物信息学分析。

Bioinformatic analysis based on the complete coding region of the MSTN gene within and among different species.

作者信息

Song X C, Xu C, Yue Z G, Wang L, Wang G W, Yang F H

机构信息

State Key Laboratory of Special Economic Animal Molecular Biology, Institute of Special Animal and Plant Sciences.

出版信息

Genet Mol Res. 2016 Apr 7;15(2):gmr5031. doi: 10.4238/gmr.15025031.

DOI:10.4238/gmr.15025031
PMID:27173201
Abstract

Myostatin, encoded by the MSTN gene (previously GDF8), is a member of the transforming growth factor-β superfamily, which normally acts to limit skeletal muscle mass by regulating the number and growth of muscle fibers. In this study, a total of 84 myostatin gene sequences with known complete coding regions (CDS) and corresponding amino acid sequences were analyzed from 17 species, and differentiation within and among species was studied using comparative genomics and bioinformatics. Characteristics of the nucleotide and amino acid sequences were also predicted. The results indicated that a total of 569 polymorphic sites, including 53 singleton variable sites and 516 parsimony informative sites, which could be sorted into 44 haplotypes, were detected from 17 species. Observed genetic diversity was higher among species than within species, and Vulpes lagopus was more polymorphic than other species. There was clear differentiation of the myostatin gene among species and the reconstructed phylogenetic tree was consistent with the NCBI taxonomy. The myostatin gene was 375-aa long in most species, except for Mus musculus (376 aa) and Danio rerio (373 aa). The amino acid sequences of myostatin were deemed hydrophilic, and had theoretical pI values of <7.0, mostly due to the acidic polypeptide. The instability index of the myostatin protein was 40.48-51.63, indicating that the polypeptide is not stable. The G+C content of the CDS nucleotide sequence in different species was 40.60-51.69%. The predicted promoter region of the Ovis aries myostatin gene was 150-220 bp upstream of the start codon.

摘要

肌生成抑制素由MSTN基因(以前称为GDF8)编码,是转化生长因子-β超家族的成员,通常通过调节肌纤维的数量和生长来限制骨骼肌质量。在本研究中,从17个物种中分析了总共84个具有已知完整编码区(CDS)和相应氨基酸序列的肌生成抑制素基因序列,并使用比较基因组学和生物信息学研究了种内和种间的差异。还预测了核苷酸和氨基酸序列的特征。结果表明,从17个物种中检测到总共569个多态性位点,包括53个单态变异位点和516个简约信息位点,这些位点可分为44个单倍型。观察到的遗传多样性在种间高于种内,北极狐比其他物种具有更多的多态性。肌生成抑制素基因在种间存在明显差异,重建的系统发育树与NCBI分类法一致。除小家鼠(376个氨基酸)和斑马鱼(373个氨基酸)外,大多数物种的肌生成抑制素基因长度为375个氨基酸。肌生成抑制素的氨基酸序列被认为是亲水性的,理论pI值<7.0,主要是由于酸性多肽。肌生成抑制素蛋白的不稳定指数为40.48 - 51.63,表明该多肽不稳定。不同物种CDS核苷酸序列的G + C含量为40.60 - 51.69%。绵羊肌生成抑制素基因的预测启动子区域位于起始密码子上游150 - 220 bp处。

相似文献

1
Bioinformatic analysis based on the complete coding region of the MSTN gene within and among different species.基于不同物种内和物种间MSTN基因完整编码区的生物信息学分析。
Genet Mol Res. 2016 Apr 7;15(2):gmr5031. doi: 10.4238/gmr.15025031.
2
Genomic cloning and promoter functional analysis of myostatin-2 in shi drum, Umbrina cirrosa: conservation of muscle-specific promoter activity.肌肉生长抑制素-2 在石斑鱼中的基因组克隆和启动子功能分析:肌肉特异性启动子活性的保守性。
Comp Biochem Physiol B Biochem Mol Biol. 2013 Feb;164(2):99-110. doi: 10.1016/j.cbpb.2012.11.003. Epub 2012 Nov 21.
3
Identification and expression characterization of the myostatin (MSTN) gene and association analysis with growth traits in the razor clam Sinonovacula constricta.缢蛏肌生成抑制素(MSTN)基因的鉴定、表达特征及其与生长性状的关联分析
Gene. 2015 Jan 25;555(2):297-304. doi: 10.1016/j.gene.2014.11.020. Epub 2014 Nov 13.
4
Characterization of a myostatin gene (MSTN1) from spotted halibut (Verasper variegatus) and association between its promoter polymorphism and individual growth performance.斑点星鲽肌抑素基因(MSTN1)的特性及其启动子多态性与个体生长性能的关联。
Comp Biochem Physiol B Biochem Mol Biol. 2012 Apr;161(4):315-22. doi: 10.1016/j.cbpb.2011.12.008. Epub 2011 Dec 24.
5
Molecular characterization and expression analysis of the myostatin gene and its association with growth traits in Noble scallop (Chlamys nobilis).华贵栉孔扇贝(Chlamys nobilis)肌肉生长抑制素基因的分子特征、表达分析及其与生长性状的关联
Comp Biochem Physiol B Biochem Mol Biol. 2017 Oct;212:24-31. doi: 10.1016/j.cbpb.2017.07.004. Epub 2017 Jul 16.
6
Molecular characterization of the myosatin gene and the effect of fasting on its expression in Chinese perch (Siniperca chuatsi).鳜鱼肌生成抑制素基因的分子特征及禁食对其表达的影响
Genet Mol Res. 2016 Apr 29;15(2):gmr8354. doi: 10.4238/gmr.15028354.
7
Molecular characterization, expression analysis of the myostatin gene and its association with growth traits in sea cucumber (Apostichopus japonicus).刺参肌肉生长抑制素基因的分子特征、表达分析及其与生长性状的关联
Comp Biochem Physiol B Biochem Mol Biol. 2016 Nov;201:12-20. doi: 10.1016/j.cbpb.2016.06.005. Epub 2016 Jun 21.
8
[Identification and characterization of myostatin gene in rough-skinned sculp, Trachidermus fasciatus].[粗皮鲀(Trachidermus fasciatus)中肌肉生长抑制素基因的鉴定与特征分析]
Dongwuxue Yanjiu. 2010 Aug;31(4):387-94. doi: 10.3724/SP.J.1141.2010.04387.
9
The myostatin gene of Mytilus chilensis evidences a high level of polymorphism and ubiquitous transcript expression.智利贻贝的肌肉生长抑制素基因表现出高度多态性和广泛的转录表达。
Gene. 2014 Feb 15;536(1):207-12. doi: 10.1016/j.gene.2013.11.067. Epub 2013 Dec 12.
10
Myostatin from the American lobster, Homarus americanus: Cloning and effects of molting on expression in skeletal muscles.美洲螯龙虾肌肉生长抑制素的克隆及其在蜕皮过程中对骨骼肌表达的影响。
Comp Biochem Physiol A Mol Integr Physiol. 2010 Dec;157(4):328-37. doi: 10.1016/j.cbpa.2010.07.024. Epub 2010 Aug 7.

引用本文的文献

1
Myostatin gene promoter: structure, conservation and importance as a target for muscle modulation.肌肉生长抑制素基因启动子:结构、保守性及其作为肌肉调节靶点的重要性
J Anim Sci Biotechnol. 2019 Apr 23;10:32. doi: 10.1186/s40104-019-0338-5. eCollection 2019.
2
Myostatin and beyond in cirrhosis: all roads lead to sarcopenia.肝硬化中的肌肉生长抑制素及其他:条条大路通肌肉减少症。
J Cachexia Sarcopenia Muscle. 2017 Dec;8(6):864-869. doi: 10.1002/jcsm.12262.