Reductions in expression of growth regulating genes in skeletal muscle with age in wild type and myostatin null mice.

Q1 Biochemistry, Genetics and Molecular Biology BMC Physiology Pub Date : 2014-03-28 DOI:10.1186/1472-6793-14-3
Jennifer C Jones, Kellie A Kroscher, Anna C Dilger
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引用次数: 7

Abstract

Background: Genes that decline in expression with age and are thought to coordinate growth cessation have been identified in various organs, but their expression in skeletal muscle is unknown. Therefore, our objective was to determine expression of these genes (Ezh2, Gpc3, Mdk, Mest, Mycn, Peg3, and Plagl1) in skeletal muscle from birth to maturity. We hypothesized that expression of these genes would decline with age in skeletal muscle but differ between sexes and between wild type and myostatin null mice.

Results: Female and male wild type and myostatin null mice (C57BL/6J background) were sacrificed by carbon dioxide asphyxiation followed by decapitation at d -7, 0, 21, 42, and 70 days of age. Whole bodies at d -7, all muscles from both hind limbs at d 0, and bicep femoris muscle from d 21, 42 and 70 were collected. Gene expression was determined by quantitative real-time PCR. In general, expression of these growth-regulating genes was reduced at d 21 compared with day 0 and d -7. Expression of Gpc3, Mest, and Peg3 was further reduced at d 42 and 70 compared with d 21, however the expression of Mycn increased from d 21 to d 42 and 70. Myostatin null mice, as expected, were heavier with increased biceps femoris weight at d 70. However, with respect to sex and genotype, there were few differences in expression. Expression of Ezh2 was increased at d 70 and expression of Mdk was increased at d 21 in myostatin null mice compared with wild type, but no other genotype effects were present. Expression of Mdk was increased in females compared to males at d 70, but no other sex effects were present.

Conclusions: Overall, these data suggest the downregulation of these growth-regulating genes with age might play a role in the coordinated cessation of muscle growth similar to organ growth but likely have a limited role in the differences between sexes or genotypes.

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野生型和肌肉生长抑制素缺失小鼠骨骼肌中生长调节基因表达随年龄的减少。
背景:随着年龄增长而表达下降的基因,被认为是协调生长停止的基因,已经在各种器官中被发现,但它们在骨骼肌中的表达尚不清楚。因此,我们的目的是确定这些基因(Ezh2、Gpc3、Mdk、Mest、Mycn、Peg3和Plagl1)在出生至成熟期间骨骼肌中的表达。我们假设这些基因在骨骼肌中的表达会随着年龄的增长而下降,但在性别之间以及野生型和肌肉生长抑制素缺失的小鼠之间存在差异。结果:雌性和雄性野生型小鼠和肌肉生长抑制素缺失小鼠(C57BL/6J背景)在-7、0、21、42和70日龄时采用二氧化碳窒息后斩首处死。在d -7时采集整个躯干,d 0时采集两后肢的所有肌肉,d 21、42和70时采集股二头肌。采用实时荧光定量PCR检测基因表达。总的来说,与第0天和第7天相比,这些生长调节基因的表达在第21天减少。与第21天相比,Gpc3、Mest和Peg3的表达在第42天和第70天进一步降低,而Mycn的表达在第21天和第42天和第70天增加。正如预期的那样,肌肉生长抑制素无效的小鼠在70岁时体重增加,股二头肌重量增加。然而,在性别和基因型方面,表达差异不大。与野生型相比,肌生长抑制素缺失小鼠Ezh2在70 d时表达增加,Mdk在21 d时表达增加,但没有其他基因型效应。Mdk的表达在70岁时女性比男性增加,但没有其他性别影响。结论:总的来说,这些数据表明,随着年龄的增长,这些生长调节基因的下调可能在肌肉生长的协调停止中发挥作用,类似于器官生长,但在性别或基因型之间的差异中可能作用有限。
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来源期刊
BMC Physiology
BMC Physiology Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
9.60
自引率
0.00%
发文量
0
期刊介绍: BMC Physiology is an open access journal publishing original peer-reviewed research articles in cellular, tissue-level, organismal, functional, and developmental aspects of physiological processes. BMC Physiology (ISSN 1472-6793) is indexed/tracked/covered by PubMed, MEDLINE, BIOSIS, CAS, EMBASE, Scopus, Zoological Record and Google Scholar.
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