Kretzschmar M, Massagué J
Cell Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Curr Opin Genet Dev. 1998 Feb;8(1):103-11. doi: 10.1016/s0959-437x(98)80069-5.
The discovery of SMAD proteins has allowed the delineation of a mechanism by which TGF-beta and related growth factors convey their signals from membrane receptors all the way into the nucleus. SMADs are directly phosphorylated and activated by the receptors and then form heteromeric SMAD-SMAD complexes that move into the nucleus where they orchestrate transcriptional responses. In rapid succession, recent reports have identified different modes of SMAD regulation by phosphorylation and have defined the SMAD domains that mediate SMAD interactions, binding to DNA or transcriptional activation. The recent discovery of antagonistic SMADs and regulatory crosstalk with Ras/MAP-kinase pathways add to our rapidly expanding understanding of this major regulatory network.
SMAD蛋白的发现,使得人们能够勾勒出一种机制,通过该机制,转化生长因子β(TGF-β)及相关生长因子能够将其信号从膜受体一直传递至细胞核。SMAD蛋白可被受体直接磷酸化并激活,随后形成异源SMAD-SMAD复合物,该复合物进入细胞核并在其中协调转录反应。最近的报告相继确定了通过磷酸化对SMAD进行调控的不同模式,并明确了介导SMAD相互作用、与DNA结合或转录激活的SMAD结构域。拮抗SMAD的最新发现以及与Ras/丝裂原活化蛋白激酶(MAP)途径的调节性串扰,加深了我们对这一主要调节网络的快速扩展的理解。