Hoogaars W M H, Barnett P, Moorman A F M, Christoffels V M
Heart Failure Research Center, Department of Anatomy and Embryology, Academic Medical Center, Amsterdam, The Netherlands.
Cell Mol Life Sci. 2007 Mar;64(6):646-60. doi: 10.1007/s00018-007-6518-z.
The heart of higher vertebrates is a structurally complicated multi-chambered pump that contracts synchronously. For its proper function a number of distinct integrated components have to be generated, including force-generating compartments, unidirectional valves, septa and a system in charge of the initiation and coordinated propagation of the depolarizing impulse over the heart. Not surprisingly, a large number of regulating factors are involved in these processes that act in complex and intertwined pathways to regulate the activity of target genes responsible for morphogenesis and function. The finding that mutations in T-box transcription factor-encoding genes in humans lead to congenital heart defects has focused attention on the importance of this family of regulators in heart development. Functional and genetic analyses in a variety of divergent species has demonstrated the critical roles of multiple T-box factor gene family members, including Tbx11, -2, -3, -5, -18 and -20, in the patterning, recruitment, specification, differentiation and growth processes underlying formation and integration of the heart components. Insight into the roles of T-box factors in these processes will enhance our understanding of heart formation and the underlying molecular regulatory pathways.
高等脊椎动物的心脏是一个结构复杂的多腔泵,能同步收缩。为了使其正常运作,必须生成许多不同的整合组件,包括产生力量的腔室、单向瓣膜、隔膜以及负责去极化冲动在心脏上起始和协调传播的系统。毫不奇怪,大量调节因子参与这些过程,它们通过复杂且相互交织的途径发挥作用,以调节负责形态发生和功能的靶基因的活性。人类中编码T盒转录因子的基因突变会导致先天性心脏缺陷这一发现,已将人们的注意力集中在这个调节因子家族在心脏发育中的重要性上。对多种不同物种进行的功能和遗传分析表明,多个T盒因子基因家族成员,包括Tbx11、-2、-3、-5、-18和-20,在心脏组件形成和整合所涉及的模式形成、募集、特化、分化和生长过程中发挥着关键作用。深入了解T盒因子在这些过程中的作用将增进我们对心脏形成及潜在分子调节途径的理解。