Henderson J R, Macalma T, Brown D, Richardson J A, Olson E N, Beckerle M C
Department of Biology, University of Utah, Salt Lake City 84112-0840, USA.
Dev Dyn. 1999 Mar;214(3):229-38. doi: 10.1002/(SICI)1097-0177(199903)214:3<229::AID-AJA6>3.0.CO;2-S.
LIM domains are double zinc-finger motifs found in many proteins that play central roles in cell differentiation. Members of the cysteine-rich protein (CRP) family display two LIM domains and are implicated in muscle development. Here we describe the characterization of one member of this family, CRP1, in the mouse. We have isolated and sequenced murine cDNAs that encode CRP1. We have determined by Northern analysis and in situ hybridization that CRP1 expression is developmentally regulated in the embryonic mouse and displays organ specific regulation in adults. The gene encoding CRP1 is expressed in the smooth muscle cells (SMCs) of the dorsal aorta at E9.5, thus illustrating that CRP1 is an early marker for SMC differentiation at that site. As development proceeds, CRP1 transcripts are observed throughout the SMC lineage, with minimal, transient expression detected in skeletal and cardiac muscle. Interestingly, although several markers of mature smooth muscle are already expressed, CRP1 expression in the bladder is not upregulated until the onset of bladder expansion at embryonic day 16.5, at which time its expression becomes very prominent. CRP1 expression persists into adulthood with prominent expression observed in both vascular and visceral smooth muscle. The results reported here define CRP1 as a general marker of smooth muscle lineages.
LIM结构域是在许多蛋白质中发现的双锌指基序,这些蛋白质在细胞分化中起核心作用。富含半胱氨酸蛋白(CRP)家族的成员具有两个LIM结构域,并与肌肉发育有关。在此,我们描述了该家族一个成员CRP1在小鼠中的特征。我们已经分离并测序了编码CRP1的小鼠cDNA。我们通过Northern分析和原位杂交确定,CRP1的表达在胚胎小鼠中受到发育调控,并且在成体中表现出器官特异性调控。编码CRP1的基因在胚胎第9.5天在背主动脉的平滑肌细胞(SMC)中表达,这表明CRP1是该部位SMC分化的早期标志物。随着发育的进行,在整个SMC谱系中都观察到CRP1转录本,在骨骼肌和心肌中检测到的表达极少且短暂。有趣的是,尽管几种成熟平滑肌标志物已经表达,但直到胚胎第16.5天膀胱开始扩张时,CRP1在膀胱中的表达才上调,此时其表达变得非常显著。CRP1的表达持续到成年期,在血管平滑肌和内脏平滑肌中均观察到显著表达。此处报道的结果将CRP1定义为平滑肌谱系的通用标志物。