Šošić Drazen, Richardson James A, Yu Kai, Ornitz David M, Olson Eric N
Department of Molecular Biology, University of Texas Southwestern Medical Center, 6000 Harry Hines Boulevard, Dallas, TX 75390, USA.
Cell. 2003 Jan 24;112(2):169-80. doi: 10.1016/s0092-8674(03)00002-3.
During Drosophila embryogenesis, the dorsal transcription factor activates the expression of twist, a transcription factor required for mesoderm formation. We show here that the mammalian twist proteins, twist-1 and -2, are induced by a cytokine signaling pathway that requires the dorsal-related protein RelA, a member of the NF-kappaB family of transcription factors. Twist-1 and -2 repress cytokine gene expression through interaction with RelA. Mice homozygous for a twist-2 null allele or doubly heterozygous for twist-1 and -2 alleles show elevated expression of proinflammatory cytokines, resulting in perinatal death from cachexia. These findings reveal an evolutionarily conserved signaling circuit in which twist proteins regulate cytokine signaling by establishing a negative feedback loop that represses the NF-kappaB-dependent cytokine pathway.
在果蝇胚胎发育过程中,背侧转录因子激活了中胚层形成所需的转录因子twist的表达。我们在此表明,哺乳动物的twist蛋白twist-1和-2是由一种细胞因子信号通路诱导产生的,该信号通路需要与背侧相关的RelA蛋白,RelA是转录因子NF-κB家族的成员。Twist-1和-2通过与RelA相互作用来抑制细胞因子基因的表达。twist-2无效等位基因的纯合小鼠或twist-1和-2等位基因的双杂合小鼠表现出促炎细胞因子表达升高,导致因恶病质而围产期死亡。这些发现揭示了一种进化上保守的信号传导回路,其中twist蛋白通过建立一个抑制NF-κB依赖性细胞因子途径的负反馈回路来调节细胞因子信号传导。