组蛋白脱乙酰基酶2
组蛋白乙酰转移酶
HDAC1型
组蛋白脱乙酰基酶
肌肉萎缩
萎缩
HDAC11型
HDAC4型
骨骼肌
组蛋白
生物
组蛋白脱乙酰基酶5
基因表达
HDAC6型
PCAF公司
乙酰化
基因
分子生物学
癌症研究
内分泌学
遗传学
作者
Adam W. Beharry,Andrew R. Judge
出处
期刊:Muscle & Nerve
[Wiley]
日期:2015-09-15
卷期号:52 (6): 1098-1101
被引量:15
摘要
ABSTRACT Introduction : Histone deacetylase (HDAC) proteins, which counter the activity of histone acetyltransferases (HATs), are necessary for normal muscle atrophy in response to several pathophysiological conditions. Despite this, it remains unknown whether a common or unique transcriptional profile of HDAC and HAT genes exist during the progression of muscle atrophy. Methods : Muscles were harvested from cast immobilized, denervated, or nutrient deprived animals for quantitative reverse transcriptase‐polymerase chain reaction analysis of HDAC and HAT gene expression. Results : The mRNA levels of Hdac2, Hdac4, Hdac6, Sirt1, p300, Cbp , and Pcaf increased, and Hdac7 decreased in skeletal muscle in each experimental model of muscle atrophy. Hdac1 and Hdac3 were increased only in cast immobilized and denervated muscles. Conclusions : While specific HDACs and HATs are increased in multiple models of muscle atrophy, increased expression of class I HDACs was unique to muscle disuse, reinforcing that specific HDAC inhibitors may be more effective than pan‐HDAC inhibitors at countering muscle atrophy. Muscle Nerve 52 : 1098–1101, 2015
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