Brown S, Biben C, Ooms L M, Maimone M, McGrath M J, Gurung R, Harvey R P, Mitchell C A
Monash University Department of Medicine, Box Hill Hospital, Nelson Road, Box Hill, Melbourne, 3128, Australia.
J Mol Cell Cardiol. 1999 Apr;31(4):837-43. doi: 10.1006/jmcc.1998.0922.
LIM proteins perform critical roles in development and tissue differentiation. The skeletal muscle LIM protein 1 (SLIM1) comprises four and a half LIM domains. Northern blot analysis demonstrated high level expression of SLIM1 mRNA in adult human skeletal muscle with intermediate expression in adult heart and lower expression in other tissues. Western blot analysis using specific affinity-purified anti-SLIM1 antipeptide antibodies demonstrated a 32 kDa polypeptide in the aorta and atria of rabbit heart, but not in vena cava, interventricular septum or ventricular muscle. SLIM1 was also demonstrated in rabbit skeletal muscle. In situ hybridization of whole mouse embryos confirmed the cardiac expression of SLIM1 was restricted to the cardiac outflow tract from embryonic day 8.5-11. No expression was seen in atrial or ventricular muscle. SLIM1 mRNA was also demonstrated in the hindbrain, neural tube and somites. The localized expression of SLIM1 to the outflow tract of the embryonic heart implies an important role for the protein in the development of this region and possibly in congenital heart anomalies involving the separation and formation of the aortic and pulmonary trunks.
LIM蛋白在发育和组织分化中发挥关键作用。骨骼肌LIM蛋白1(SLIM1)由四个半LIM结构域组成。Northern印迹分析表明,SLIM1 mRNA在成人骨骼肌中高表达,在成人心脏中中等表达,在其他组织中低表达。使用特异性亲和纯化的抗SLIM1抗肽抗体进行的Western印迹分析表明,在兔心脏的主动脉和心房中有一条32 kDa的多肽,但在腔静脉、室间隔或心室肌中没有。在兔骨骼肌中也检测到了SLIM1。对整个小鼠胚胎进行原位杂交证实,从胚胎第8.5天到11天,SLIM1的心脏表达仅限于心脏流出道。在心房或心室肌中未观察到表达。在小鼠后脑、神经管和体节中也检测到了SLIM1 mRNA。SLIM1在胚胎心脏流出道的局部表达意味着该蛋白在该区域的发育中以及可能在涉及主动脉和肺动脉干分离和形成的先天性心脏异常中发挥重要作用。