Roux Marine, Zaffran Stéphane
Aix Marseille Université, GMGF UMRS910, Faculté de Médecine, 27 Bd Jean Moulin, Marseille 13385, France.
Inserm U910, Faculté de Médecine, 27 Bd Jean Moulin, Marseille 13005, France.
J Dev Biol. 2016 Mar 24;4(2):14. doi: 10.3390/jdb4020014.
Congenital heart defects (CHD) are the leading cause of death in the first year of life. Over the past 20 years, much effort has been focused on unraveling the genetic bases of CHD. In particular, studies in human genetics coupled with those of model organisms have provided valuable insights into the gene regulatory networks underlying CHD pathogenesis. genes encode transcription factors that are required for the patterning of the anterior-posterior axis in the embryo. In this review, we focus on the emerging role of anteriorly expressed genes (, , and ) in cardiac development, specifically their contribution to patterning of cardiac progenitor cells and formation of the great arteries. Recent evidence regarding the cooperative regulation of heart development by Hox proteins with members of the TALE-class of homeodomain proteins such as Pbx and Meis transcription factors is also discussed. These findings are highly relevant to human pathologies as they pinpoint new genes that increase susceptibility to cardiac anomalies and provide novel mechanistic insights into CHD.
先天性心脏缺陷(CHD)是一岁以内婴儿死亡的主要原因。在过去20年里,人们付出了很多努力来揭示CHD的遗传基础。特别是,人类遗传学研究与模式生物研究相结合,为CHD发病机制背后的基因调控网络提供了有价值的见解。基因编码转录因子,这些转录因子是胚胎前后轴模式形成所必需的。在这篇综述中,我们重点关注在心脏发育中起新兴作用的前表达基因(、和),特别是它们对心脏祖细胞模式形成和大动脉形成的贡献。还讨论了关于Hox蛋白与TALE类同源域蛋白成员(如Pbx和Meis转录因子)协同调节心脏发育的最新证据。这些发现与人类病理学高度相关,因为它们确定了增加心脏异常易感性的新基因,并为CHD提供了新的机制见解。