Verweij Walter, Spelt Cornelis E, Bliek Mattijs, de Vries Michel, Wit Niek, Faraco Marianna, Koes Ronald, Quattrocchio Francesca M
Department of Molecular and Cell Biology, VU University, 1071 HK Amsterdam, The Netherlands.
Department of Molecular and Cell Biology, VU University, 1071 HK Amsterdam, The Netherlands Swammerdam Institute for Life Sciences, University of Amsterdam, 1012 WX Amsterdam, The Netherlands.
Plant Cell. 2016 Mar;28(3):786-803. doi: 10.1105/tpc.15.00608. Epub 2016 Mar 14.
The WD40 proteins ANTHOCYANIN11 (AN11) from petunia (Petunia hybrida) and TRANSPARENT TESTA GLABRA1 (TTG1) from Arabidopsis thaliana and associated basic helix-loop-helix (bHLH) and MYB transcription factors activate a variety of differentiation processes. In petunia petals, AN11 and the bHLH protein AN1 activate, together with the MYB protein AN2, anthocyanin biosynthesis and, together with the MYB protein PH4, distinct genes, such as PH1 and PH5, that acidify the vacuole. To understand how AN1 and AN11 activate anthocyanin biosynthetic and PH genes independently, we isolated PH3. We found that PH3 is a target gene of the AN11-AN1-PH4 complex and encodes a WRKY protein that can bind to AN11 and is required, in a feed-forward loop, together with AN11-AN1-PH4 for transcription of PH5. PH3 is highly similar to TTG2, which regulates hair development, tannin accumulation, and mucilage production in Arabidopsis. Like PH3, TTG2 can bind to petunia AN11 and the Arabidopsis homolog TTG1, complement ph3 in petunia, and reactivate the PH3 target gene PH5. Our findings show that the specificity of WD40-bHLH-MYB complexes is in part determined by interacting proteins, such as PH3 and TTG2, and reveal an unanticipated similarity in the regulatory circuitry that controls petunia vacuolar acidification and Arabidopsis hair development.
矮牵牛(Petunia hybrida)中的WD40蛋白花青素11(AN11)和拟南芥中的透明种皮无毛1(TTG1)以及相关的碱性螺旋-环-螺旋(bHLH)和MYB转录因子可激活多种分化过程。在矮牵牛花瓣中,AN11和bHLH蛋白AN1与MYB蛋白AN2一起激活花青素生物合成,并与MYB蛋白PH4一起激活使液泡酸化的不同基因,如PH1和PH5。为了了解AN1和AN11如何独立激活花青素生物合成基因和PH基因,我们分离出了PH3。我们发现PH3是AN11-AN1-PH4复合物的靶基因,编码一种WRKY蛋白,该蛋白可与AN11结合,并且在前馈环中与AN11-AN1-PH4一起是PH5转录所必需的。PH3与TTG2高度相似,TTG2在拟南芥中调节毛发发育、单宁积累和黏液产生。与PH3一样,TTG2可以与矮牵牛AN11和拟南芥同源物TTG1结合,在矮牵牛中互补ph3,并重新激活PH3靶基因PH5。我们的研究结果表明,WD40-bHLH-MYB复合物的特异性部分由相互作用的蛋白如PH3和TTG2决定,并揭示了控制矮牵牛液泡酸化和拟南芥毛发发育的调控回路中存在意想不到的相似性。