Cordero Dwight, Marcucio Ralph, Hu Diane, Gaffield William, Tapadia Minal, Helms Jill A
University of California at San Francisco, San Francisco, California, USA.
J Clin Invest. 2004 Aug;114(4):485-94. doi: 10.1172/JCI19596.
One of the most perplexing questions in clinical genetics is why patients with identical gene mutations oftentimes exhibit radically different clinical features. This inconsistency between genotype and phenotype is illustrated in the malformation spectrum of holoprosencephaly (HPE). Family members carrying identical mutations in sonic hedgehog (SHH) can exhibit a variety of facial features ranging from cyclopia to subtle midline asymmetries. Such intrafamilial variability may arise from environmental factors acting in conjunction with gene mutations that collectively reduce SHH activity below a critical threshold. We undertook a series of experiments to test the hypothesis that modifying the activity of the SHH signaling pathway at discrete periods of embryonic development could account for the phenotypic spectrum of HPE. Exposing avian embryos to cyclopamine during critical periods of craniofacial development recreated a continuum of HPE-related defects. The craniofacial malformations included hypotelorism, midfacial hypoplasia, and facial clefting and were not the result of excessive crest cell apoptosis. Rather, they resulted from molecular reprogramming of an organizing center whose activity controls outgrowth and patterning of the mid and upper face. Collectively, these data reveal one mechanism by which the variable expressivity of a disorder such as HPE can be produced through temporal disruption of a single molecular pathway.
临床遗传学中最令人困惑的问题之一是,具有相同基因突变的患者为何常常表现出截然不同的临床特征。全前脑畸形(HPE)的畸形谱就体现了基因型与表型之间的这种不一致性。携带音猬因子(SHH)相同突变的家庭成员可表现出从独眼畸形到细微中线不对称等各种各样的面部特征。这种家族内变异性可能源于环境因素与基因突变共同作用,使SHH活性总体降低至临界阈值以下。我们开展了一系列实验,以检验这样一个假说:在胚胎发育的不同阶段改变SHH信号通路的活性可以解释HPE的表型谱。在颅面发育的关键时期,将禽类胚胎暴露于环杷明中,重现了一系列与HPE相关的缺陷。颅面畸形包括眼距过窄、面中部发育不全和面部裂隙,并非由于嵴细胞过度凋亡所致。相反地,它们是由一个组织中心的分子重编程导致的,该组织中心的活性控制着中面部和上半面部的生长和模式形成。总体而言,这些数据揭示了一种机制,通过这种机制,像HPE这样的疾病的可变表达性可通过对单一分子通路的时间性破坏而产生。