Oron Efrat, Mannervik Mattias, Rencus Sigal, Harari-Steinberg Orit, Neuman-Silberberg Shira, Segal Daniel, Chamovitz Daniel A
Department of Plant Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Development. 2002 Oct;129(19):4399-409. doi: 10.1242/dev.129.19.4399.
The COP9 signalosome (CSN) is an essential eight-subunit repressor of light-regulated development in Arabidopsis. This complex has also been identified in animals, though its developmental role remains obscure. CSN subunits have been implicated in various cellular processes, suggesting a possible role for the CSN as an integrator of multiple signaling pathways. In order to elucidate the function of the CSN in animals, a Drosophila model system has previously been established. Gel-filtration analysis with antibodies against CSN subunits 4, 5 and 7 revealed that these proteins act as a complex in Drosophila that is similar in size to the plant and mammalian complexes. Null mutations in either one of two subunits, CSN4 or CSN5, are larval lethal. Successful embryogenesis appears to be a consequence of maternal contribution of the complex. Biochemical analysis indicates that the different subunits are found in both CSN-dependent and CSN-independent forms, and that these forms are differentially affected by the mutations. Phenotypic characterization of these two mutants indicates that they show both shared and unique phenotypes, which suggest specific roles for each subunit. Both mutants have defective oocyte and embryo patterning, and defects in response to DNA damage, while csn5 mutants develop melanotic tumors and csn4 mutants have phenotypes reminiscent of defects in ecdysone signaling.
COP9信号体(CSN)是拟南芥中光调控发育必不可少的八亚基阻遏物。该复合体在动物中也已被鉴定出来,但其在发育中的作用仍不清楚。CSN亚基参与了各种细胞过程,这表明CSN可能作为多种信号通路的整合者发挥作用。为了阐明CSN在动物中的功能,之前已建立了果蝇模型系统。用针对CSN亚基4、5和7的抗体进行凝胶过滤分析表明,这些蛋白质在果蝇中作为一个复合体起作用,其大小与植物和哺乳动物的复合体相似。CSN4或CSN5这两个亚基中的任何一个发生无效突变都是幼虫致死的。成功的胚胎发生似乎是该复合体母源贡献的结果。生化分析表明,不同的亚基以CSN依赖和CSN非依赖的形式存在,并且这些形式受到突变的不同影响。这两个突变体的表型特征表明它们表现出共同和独特的表型,这表明每个亚基都有特定的作用。两个突变体都有缺陷的卵母细胞和胚胎模式,以及对DNA损伤反应的缺陷,而csn5突变体发展出黑色素瘤,csn4突变体的表型让人联想到蜕皮激素信号传导缺陷。