Swoap S J, Haddad F, Bodell P, Baldwin K M
Department of Physiology and Biophysics, University of California, Irvine 92717, USA.
Am J Physiol. 1995 Oct;269(4 Pt 1):C1025-33. doi: 10.1152/ajpcell.1995.269.4.C1025.
In the rat left ventricle, both pressure overload induced by abdominal aortic constriction (Abcon) and caloric restriction (CR) induce an increase in the steady-state level of the beta-myosin heavy chain (MHC) protein and mRNA. Both models also induce a concomitant decrease in the alpha-MHC protein and mRNA. The goals of this study were to 1) determine if the changes in MHC expression in the models are due to altered transcription and 2) identify the relative levels of some key factors interacting with the regulatory regions of these genes. Female Sprague-Dawley rats were randomly assigned to the following groups: 1) normal control (NC), 2) Abcon, and 3) CR. After 5 wk of experimental manipulations, myocardial nuclei were isolated. These nuclei were used for 1) nuclear run-on assays or 2) nuclear extract, which was prepared and used for gel mobility shift assays (GMSAs). Nuclear run-on assays demonstrated that the increase in beta-MHC mRNA and protein expression in both Abcon and CR can be at least partially attributed to increased transcription. The concomitant decrease in alpha-MHC content can similarly be attributed to a decrease in transcription of this gene. Furthermore, GMSAs demonstrate that nuclear extract from each group interact differently with certain elements known to be important for expression in vitro. CR nuclear extracts have a 25.6 +/- 7.2% decrease (P < 0.05 vs. NC) in interaction with a thyroid-responsive element, a potential repressor of beta-MHC transcription.(ABSTRACT TRUNCATED AT 250 WORDS)
在大鼠左心室中,腹主动脉缩窄(Abcon)诱导的压力过载和热量限制(CR)均会导致β-肌球蛋白重链(MHC)蛋白和mRNA的稳态水平升高。两种模型还会同时导致α-MHC蛋白和mRNA水平降低。本研究的目的是:1)确定模型中MHC表达的变化是否由于转录改变所致;2)确定与这些基因调控区域相互作用的一些关键因子的相对水平。将雌性Sprague-Dawley大鼠随机分为以下几组:1)正常对照(NC)组、2)Abcon组和3)CR组。经过5周的实验处理后,分离心肌细胞核。这些细胞核用于:1)核转录分析;2)制备核提取物并用于凝胶迁移率变动分析(GMSA)。核转录分析表明,Abcon组和CR组中β-MHC mRNA和蛋白表达的增加至少部分归因于转录增加。α-MHC含量的同时降低同样可归因于该基因转录的减少。此外,GMSA表明,每组的核提取物与某些已知对体外表达很重要的元件的相互作用不同。CR组的核提取物与甲状腺反应元件(β-MHC转录的潜在抑制因子)的相互作用降低了25.6±7.2%(与NC组相比,P<0.05)。