Alexander T Mikhailov, Mario Torrado
Developmental Biology Group, Institute of Health Sciences, University of La Coruña, La Coruña, Spain.
Int J Dev Biol. 2008;52(7):811-21. doi: 10.1387/ijdb.082655am.
It has been proposed that the ankyrin repeat domain 1 (ANKRD1) factor (also known as CARP) plays a critical role in transcriptional regulation, myofibrillar assembly and stretch sensing during heart development and cardiac insults. ANKRD1/CARP has also been reported to negatively regulate cardiac gene expression in cell-based promoter-reporter assays. Consequently, rapid up-regulation of the ankrd1 gene in myocardium in response to developmental stimuli or pathological insults has tended to be interpreted in the context of the inhibitory effects of ANKRD1 on cardiomyocyte gene expression. Surprisingly, a total ankrd1 knockout resulted in a complete lack of phenotype, suggesting that ANKRD1/CARP is not crucial for regulation of cardiac gene expression in vivo. In this essay, we summarize (1) the accumulated evidence for the apparent multifunctional properties of this enigmatic protein, (2) the distinct chamber-dependent regulation of ankrd1 expression patterns in the heart, both during development and cardiac injury, and (3) ANKRD1 involvement in networks regulating adaptation of the myocardium to stress. Whenever feasible, we present the results obtained in patients together with those obtained in the relevant animal and cellular models. A close examination of the findings still fails to define ANKRD1 as a negative regulator of cardiac gene expression in vivo, but rather indicates that its augmented expression can represent an adaptive response of the myocardium to stress both during development and various heart insults.
有人提出,锚蛋白重复结构域1(ANKRD1)因子(也称为CARP)在心脏发育和心脏损伤期间的转录调控、肌原纤维组装和拉伸感知中起关键作用。在基于细胞的启动子-报告基因分析中,ANKRD1/CARP也被报道对心脏基因表达起负调控作用。因此,心肌中ankrd1基因响应发育刺激或病理损伤而快速上调,往往被解释为ANKRD1对心肌细胞基因表达的抑制作用。令人惊讶的是,完全敲除ankrd1导致完全没有表型,这表明ANKRD1/CARP对体内心脏基因表达的调控并非至关重要。在本文中,我们总结了:(1)关于这种神秘蛋白质明显的多功能特性的累积证据;(2)在发育和心脏损伤期间,ankrd1在心脏中不同腔室依赖性的表达模式调控;(3)ANKRD1参与调节心肌对压力适应的网络。只要可行,我们就会呈现患者以及相关动物和细胞模型中获得的结果。对这些发现的仔细研究仍然未能将ANKRD1定义为体内心脏基因表达的负调控因子,反而表明其表达增加可能代表心肌在发育和各种心脏损伤期间对压力的适应性反应。