Massagué Joan, Seoane Joan, Wotton David
Cancer Biology and Genetics Program, Howard Hughes Medical Institute, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Genes Dev. 2005 Dec 1;19(23):2783-810. doi: 10.1101/gad.1350705.
Smad transcription factors lie at the core of one of the most versatile cytokine signaling pathways in metazoan biology-the transforming growth factor-beta (TGFbeta) pathway. Recent progress has shed light into the processes of Smad activation and deactivation, nucleocytoplasmic dynamics, and assembly of transcriptional complexes. A rich repertoire of regulatory devices exerts control over each step of the Smad pathway. This knowledge is enabling work on more complex questions about the organization, integration, and modulation of Smad-dependent transcriptional programs. We are beginning to uncover self-enabled gene response cascades, graded Smad response mechanisms, and Smad-dependent synexpression groups. Our growing understanding of TGFbeta signaling through the Smad pathway provides general principles for how animal cells translate complex inputs into concrete behavior.
Smad转录因子处于后生动物生物学中最具通用性的细胞因子信号通路之一——转化生长因子-β(TGFβ)通路的核心位置。最近的研究进展已阐明了Smad激活与失活、核质动力学以及转录复合物组装的过程。一系列丰富的调控机制对Smad通路的每一步进行控制。这些知识有助于研究关于Smad依赖的转录程序的组织、整合及调节等更复杂的问题。我们开始揭示自我激活的基因反应级联、分级Smad反应机制以及Smad依赖的协同表达组。我们对通过Smad通路的TGFβ信号传导的日益深入的理解,为动物细胞如何将复杂输入转化为具体行为提供了一般原则。