School of Life Sciences, Arizona State University, Tempe, Arizona 85287-4501, USA.
Genetics. 2011 Nov;189(3):809-24. doi: 10.1534/genetics.111.133801. Epub 2011 Aug 25.
It is well known that the Dpp signal transducer Mad is activated by phosphorylation at its carboxy-terminus. The role of phosphorylation on other regions of Mad is not as well understood. Here we report that the phosphorylation of Mad in the linker region by the Wg antagonist Zw3 (homolog of vertebrate Gsk3-β) regulates the development of sensory organs in the anterior-dorsal quadrant of the wing. Proneural expression of Mad-RNA interference (RNAi) or a Mad transgene with its Zw3/Gsk3-β phosphorylation sites mutated (MGM) generated wings with ectopic sensilla and chemosensory bristle duplications. Studies with pMad-Gsk (an antibody specific to Zw3/Gsk3-β-phosphorylated Mad) in larval wing disks revealed that this phosphorylation event is Wg dependent (via an unconventional mechanism), is restricted to anterior-dorsal sensory organ precursors (SOP) expressing Senseless (Sens), and is always co-expressed with the mitotic marker phospho-histone3. Quantitative analysis in both Mad-RNAi and MGM larval wing disks revealed a significant increase in the number of Sens SOP. We conclude that the phosphorylation of Mad by Zw3 functions to prevent the self-renewal of Sens SOP, perhaps facilitating their differentiation via asymmetric division. The conservation of Zw3/Gsk3-β phosphorylation sites in vertebrate homologs of Mad (Smads) suggests that this pathway, the first transforming growth factor β-independent role for any Smad protein, may be widely utilized for regulating mitosis during development.
众所周知,Dpp 信号转导因子 Mad 通过其羧基末端的磷酸化而被激活。Mad 上其他区域磷酸化的作用还不是很清楚。在这里,我们报告了 Wg 拮抗剂 Zw3(脊椎动物 Gsk3-β 的同源物)对 Mad 连接区的磷酸化作用,调节了翅膀前背象限感觉器官的发育。Mad-RNAi(RNA 干扰)的神经前体表达或其 Zw3/Gsk3-β 磷酸化位点突变的 Mad 转基因(MGM)产生了具有异位感器和化学感觉刚毛重复的翅膀。用 pMad-Gsk(一种针对 Zw3/Gsk3-β 磷酸化 Mad 的抗体)在幼虫翅膀盘中进行的研究表明,这种磷酸化事件依赖于 Wg(通过一种非常规机制),仅限于表达 Senseless(Sens)的前背感觉器官前体(SOP),并且总是与有丝分裂标志物磷酸化组蛋白 3 共表达。在 Mad-RNAi 和 MGM 幼虫翅膀盘中的定量分析显示,Sens SOP 的数量显著增加。我们得出结论,Zw3 对 Mad 的磷酸化作用可防止 Sens SOP 的自我更新,可能通过不对称分裂促进它们的分化。在脊椎动物 Mad(Smads)同源物中的 Zw3/Gsk3-β 磷酸化位点的保守性表明,这条途径是任何 Smad 蛋白的第一个转化生长因子 β 独立作用途径,可能广泛用于调节发育过程中的有丝分裂。