Browning C L, Culberson D E, Aragon I V, Fillmore R A, Croissant J D, Schwartz R J, Zimmer W E
Department of Structural and Cellular Biology, University of South Alabama, Mobile, Alabama, 36688, USA.
Dev Biol. 1998 Feb 1;194(1):18-37. doi: 10.1006/dbio.1997.8808.
Serum response factor (SRF) is a MADS box transcription factor that has been shown to be important in the regulation of a variety of muscle-specific genes. We have previously shown SRF to be a major component of multiple cis/trans interactions found along the smooth muscle gamma-actin (SMGA) promoter. In the studies reported here, we have further characterized the role of SRF in the regulation of the SMGA gene in the developing gizzard. EMSA analyses, using nuclear extracts derived from gizzards at various stages in development, showed that the SRF-containing complexes were not present early in gizzard smooth muscle development, but appeared as development progressed. We observed an increase in SRF protein and mRNA levels during gizzard development by Western and Northern blot analyses, with a large increase just preceding an increase in SMGA expression. Thus, changes in SRF DNA-binding activity were paralleled with increased SRF gene expression. Immunohistochemical analyses demonstrated a correspondence of SRF and SMGA expression in differentiating visceral smooth muscle cells (SMCs) during gizzard tissue development. This correspondence of SRF and SMGA expression was also observed in cultured smooth muscle mesenchyme induced to express differentiated gene products in vitro. In gene transfer experiments with SMGA promoter-luciferase reporter gene constructs we observed four- to fivefold stronger SMGA promoter activity in differentiated SMCs relative to replicating visceral smooth muscle cells. Further, we demonstrate the ability of a dominant negative SRF mutant protein to specifically inhibit transcription of the SMGA promoter in visceral smooth muscle, directly linking SRF with the control of SMGA gene expression. Taken together, these data suggest that SRF plays a prominent role in the developmental regulation of the SMGA gene.
血清反应因子(SRF)是一种MADS盒转录因子,已被证明在多种肌肉特异性基因的调控中起重要作用。我们之前已经证明SRF是平滑肌γ-肌动蛋白(SMGA)启动子上发现的多个顺式/反式相互作用的主要成分。在本文报道的研究中,我们进一步阐明了SRF在发育中的砂囊中SMGA基因调控中的作用。使用来自不同发育阶段砂囊的核提取物进行的电泳迁移率变动分析(EMSA)表明,含SRF的复合物在砂囊平滑肌发育早期不存在,但随着发育进程而出现。通过蛋白质免疫印迹和Northern印迹分析,我们观察到在砂囊发育过程中SRF蛋白和mRNA水平增加,在SMGA表达增加之前大幅增加。因此,SRF DNA结合活性的变化与SRF基因表达的增加平行。免疫组织化学分析表明,在砂囊组织发育过程中,SRF和SMGA在分化的内脏平滑肌细胞(SMC)中的表达具有对应关系。在体外诱导表达分化基因产物的培养平滑肌间充质中也观察到SRF和SMGA表达的这种对应关系。在用SMGA启动子 - 荧光素酶报告基因构建体进行的基因转移实验中,我们观察到相对于增殖的内脏平滑肌细胞,分化的SMC中SMGA启动子活性强四到五倍。此外,我们证明了显性负性SRF突变蛋白能够特异性抑制内脏平滑肌中SMGA启动子的转录,直接将SRF与SMGA基因表达的控制联系起来。综上所述,这些数据表明SRF在SMGA基因的发育调控中起重要作用。