Suppr超能文献

小鼠骨骼肌肥大和再生过程中上调基因保守集的鉴定。

Identification of a conserved set of upregulated genes in mouse skeletal muscle hypertrophy and regrowth.

作者信息

Chaillou Thomas, Jackson Janna R, England Jonathan H, Kirby Tyler J, Richards-White Jena, Esser Karyn A, Dupont-Versteegden Esther E, McCarthy John J

机构信息

Center for Muscle Biology, University of Kentucky, Lexington, Kentucky; Department of Physiology, College of Medicine, University of Kentucky, Lexington, Kentucky;

Center for Muscle Biology, University of Kentucky, Lexington, Kentucky; Department of Physiology, College of Medicine, University of Kentucky, Lexington, Kentucky; Department of Rehabilitation Sciences, College of Health Sciences, University of Kentucky, Lexington, Kentucky.

出版信息

J Appl Physiol (1985). 2015 Jan 1;118(1):86-97. doi: 10.1152/japplphysiol.00351.2014. Epub 2014 Nov 13.

Abstract

The purpose of this study was to compare the gene expression profile of mouse skeletal muscle undergoing two forms of growth (hypertrophy and regrowth) with the goal of identifying a conserved set of differentially expressed genes. Expression profiling by microarray was performed on the plantaris muscle subjected to 1, 3, 5, 7, 10, and 14 days of hypertrophy or regrowth following 2 wk of hind-limb suspension. We identified 97 differentially expressed genes (≥2-fold increase or ≥50% decrease compared with control muscle) that were conserved during the two forms of muscle growth. The vast majority (∼90%) of the differentially expressed genes was upregulated and occurred at a single time point (64 out of 86 genes), which most often was on the first day of the time course. Microarray analysis from the conserved upregulated genes showed a set of genes related to contractile apparatus and stress response at day 1, including three genes involved in mechanotransduction and four genes encoding heat shock proteins. Our analysis further identified three cell cycle-related genes at day and several genes associated with extracellular matrix (ECM) at both days 3 and 10. In conclusion, we have identified a core set of genes commonly upregulated in two forms of muscle growth that could play a role in the maintenance of sarcomere stability, ECM remodeling, cell proliferation, fast-to-slow fiber type transition, and the regulation of skeletal muscle growth. These findings suggest conserved regulatory mechanisms involved in the adaptation of skeletal muscle to increased mechanical loading.

摘要

本研究的目的是比较经历两种生长形式(肥大和再生)的小鼠骨骼肌的基因表达谱,以确定一组保守的差异表达基因。在进行了2周后肢悬吊的比目鱼肌上,分别进行1、3、5、7、10和14天的肥大或再生处理后,通过微阵列进行表达谱分析。我们鉴定出97个差异表达基因(与对照肌肉相比,增加≥2倍或减少≥50%),这些基因在两种肌肉生长形式中是保守的。绝大多数(约90%)差异表达基因上调,且出现在单个时间点(86个基因中的64个),最常见的是在时间进程的第一天。对保守上调基因的微阵列分析显示,在第1天有一组与收缩装置和应激反应相关的基因,包括3个参与机械转导的基因和4个编码热休克蛋白的基因。我们的分析进一步在第1天鉴定出3个细胞周期相关基因,在第3天和第10天鉴定出几个与细胞外基质(ECM)相关的基因。总之,我们已经鉴定出一组在两种肌肉生长形式中共同上调的核心基因,这些基因可能在维持肌节稳定性、ECM重塑、细胞增殖、快肌纤维向慢肌纤维类型转变以及骨骼肌生长调节中发挥作用。这些发现提示了参与骨骼肌适应增加的机械负荷的保守调节机制。

相似文献

1
Identification of a conserved set of upregulated genes in mouse skeletal muscle hypertrophy and regrowth.
J Appl Physiol (1985). 2015 Jan 1;118(1):86-97. doi: 10.1152/japplphysiol.00351.2014. Epub 2014 Nov 13.
2
Time course of gene expression during mouse skeletal muscle hypertrophy.
J Appl Physiol (1985). 2013 Oct 1;115(7):1065-74. doi: 10.1152/japplphysiol.00611.2013. Epub 2013 Jul 18.
4
Changes in muscle fiber contractility and extracellular matrix production during skeletal muscle hypertrophy.
J Appl Physiol (1985). 2017 Mar 1;122(3):571-579. doi: 10.1152/japplphysiol.00719.2016. Epub 2016 Dec 15.
8
Absence of heat shock transcription factor 1 retards the regrowth of atrophied soleus muscle in mice.
J Appl Physiol (1985). 2011 Oct;111(4):1142-9. doi: 10.1152/japplphysiol.00471.2011. Epub 2011 Aug 4.
9
Calcineurin-mediated slow-type fiber expression and growth in reloading condition.
Med Sci Sports Exerc. 2006 Jun;38(6):1065-72. doi: 10.1249/01.mss.0000222833.43520.6e.
10
Target genes of myostatin loss-of-function in muscles of late bovine fetuses.
BMC Genomics. 2007 Mar 1;8:63. doi: 10.1186/1471-2164-8-63.

引用本文的文献

2
Combining Gene Mutation with Expression of Candidate Genes to Improve Diagnosis of Escobar Syndrome.
Genes (Basel). 2022 Sep 27;13(10):1748. doi: 10.3390/genes13101748.
3
Ranolazine Counteracts Strength Impairment and Oxidative Stress in Aged Sarcopenic Mice.
Metabolites. 2022 Jul 18;12(7):663. doi: 10.3390/metabo12070663.
6
Acute sprint exercise transcriptome in human skeletal muscle.
PLoS One. 2019 Oct 24;14(10):e0223024. doi: 10.1371/journal.pone.0223024. eCollection 2019.
7
The impact of skeletal muscle contraction on CD146Lin pericytes.
Am J Physiol Cell Physiol. 2019 Nov 1;317(5):C1011-C1024. doi: 10.1152/ajpcell.00156.2019. Epub 2019 Aug 21.
9
Postnatal tendon growth and remodeling require platelet-derived growth factor receptor signaling.
Am J Physiol Cell Physiol. 2018 Apr 1;314(4):C389-C403. doi: 10.1152/ajpcell.00258.2017. Epub 2017 Dec 13.

本文引用的文献

2
Causal analysis approaches in Ingenuity Pathway Analysis.
Bioinformatics. 2014 Feb 15;30(4):523-30. doi: 10.1093/bioinformatics/btt703. Epub 2013 Dec 13.
3
Dysferlin stabilizes stress-induced Ca2+ signaling in the transverse tubule membrane.
Proc Natl Acad Sci U S A. 2013 Dec 17;110(51):20831-6. doi: 10.1073/pnas.1307960110. Epub 2013 Dec 3.
4
Time course of gene expression during mouse skeletal muscle hypertrophy.
J Appl Physiol (1985). 2013 Oct 1;115(7):1065-74. doi: 10.1152/japplphysiol.00611.2013. Epub 2013 Jul 18.
8
Muscle-specific microRNA1 (miR1) targets heat shock protein 70 (HSP70) during dexamethasone-mediated atrophy.
J Biol Chem. 2013 Mar 1;288(9):6663-78. doi: 10.1074/jbc.M112.390369. Epub 2013 Jan 6.
9
Alterations in osteopontin modify muscle size in females in both humans and mice.
Med Sci Sports Exerc. 2013 Jun;45(6):1060-8. doi: 10.1249/MSS.0b013e31828093c1.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验