Arbouzova Natalia I, Bach Erika A, Zeidler Martin P
Department of Molecular Developmental Biology, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
Curr Biol. 2006 Jan 10;16(1):80-8. doi: 10.1016/j.cub.2005.11.033.
A limited number of evolutionarily conserved signal transduction pathways are repeatedly reused during development to regulate a wide range of processes. Here we describe a new negative regulator of JAK/STAT signaling and identify a potential mechanism by which the pleiotropy of responses resulting from pathway activation is generated in vivo. As part of a genetic interaction screen, we have identified Ken & Barbie (Ken) , which is an ortholog of the mammalian proto-oncogene BCL6 , as a negative regulator of the JAK/STAT pathway. Ken genetically interacts with the pathway in vivo and recognizes a DNA consensus sequence overlapping that of STAT92E in vitro. Tissue culture-based assays demonstrate the existence of Ken-sensitive and Ken-insensitive STAT92E binding sites, while ectopically expressed Ken is sufficient to downregulate a subset of JAK/STAT pathway target genes in vivo. Finally, we show that endogenous Ken specifically represses JAK/STAT-dependent expression of ventral veins lacking (vvl) in the posterior spiracles. Ken therefore represents a novel regulator of JAK/STAT signaling whose dynamic spatial and temporal expression is capable of selectively modulating the transcriptional repertoire elicited by activated STAT92E in vivo.
在发育过程中,数量有限的进化保守信号转导通路会被反复用于调控多种过程。在此,我们描述了一种新的JAK/STAT信号负调控因子,并确定了一种在体内产生通路激活所致多效性反应的潜在机制。作为遗传相互作用筛选的一部分,我们鉴定出Ken & Barbie(Ken),它是哺乳动物原癌基因BCL6的直系同源物,作为JAK/STAT通路的负调控因子。Ken在体内与该通路发生遗传相互作用,并且在体外识别与STAT92E重叠的DNA共有序列。基于组织培养的分析表明存在对Ken敏感和不敏感的STAT92E结合位点,而异位表达的Ken足以在体内下调JAK/STAT通路靶基因的一个子集。最后,我们表明内源性Ken特异性抑制后气门中缺乏腹侧静脉(vvl)的JAK/STAT依赖性表达。因此,Ken代表了一种新的JAK/STAT信号调节因子,其动态的时空表达能够在体内选择性地调节由激活的STAT92E引发的转录谱。