Zhou Limei, Zheng Kaijie, Wang Xiaoyu, Tian Hainan, Wang Xianling, Wang Shucai
Key Laboratory of Molecular Epigenetics of Ministry of Education and Key Laboratory of Vegetation Ecology of Ministry of Education, Northeast Normal University Changchun, China.
Front Plant Sci. 2014 Jun 10;5:262. doi: 10.3389/fpls.2014.00262. eCollection 2014.
In Arabidopsis, trichome formation is regulated by the interplay of R3 MYBs and several others transcription factors including the WD40-repeat protein TRANSPARENT TESTA GLABRA1 (TTG1), the R2R3 MYB transcription factor GLABRA1 (GL1), the bHLH transcription factor GLABRA3 (GL3) or ENHANCER OF GLABRA3 (EGL3), and the homeodomain protein GLABRA2 (GL2). R3 MYBs including TRICHOMELESS1 (TCL1), TCL2, TRYPTICHON (TRY), CAPRICE (CPC), ENHANCER OF TRY AND CPC1 (ETC1), ETC2 and ETC3 negatively regulate trichome formation by competing with GL1 for binding GL3 or EGL3, thus blocking the formation of TTG1-GL3/EGL3-GL1, an activator complex required for the activation of the trichome positive regulator gene GL2. However, it is largely unknown if R3 MYBs in other plant species especially woody plants have similar functions. By BLASTing the Populus trichocarpa protein database using the entire amino acid sequence of TCL1, an Arabidopsis R3 MYB transcription factor, we identified a total of eight R3 MYB transcription factor genes in poplar, namely P. trichocarpa TRICHOMELESS1 through 8 (PtrTCL1-PtrTCL8). The amino acid signature required for interacting with bHLH transcription factors and the amino acids required for cell-to-cell movement of R3 MYBs are not fully conserved in all PtrTCLs. When tested in Arabidopsis protoplasts, however, all PtrTCLs interacted with GL3. Expressing each of the eight PtrTCL genes in Arabidopsis resulted in either glabrous phenotypes or plants with reduced trichome numbers, and expression levels of GL2 in all transgenic plants tested were greatly reduced. Expression of PtrTCL1 under the control of TCL1 native promoter almost completely complemented the mutant phenotype of tcl. In contrast, expression of PtrTCL1 under the control of TRY native promoter in the try mutant, or under the control of CPC native promoter in the cpc mutant resulted in glabrous phenotypes, suggesting that PtrTCL1 functions similarly to TCL1, but not TRY and CPC.
在拟南芥中,表皮毛的形成受R3 MYB转录因子与其他几种转录因子相互作用的调控,这些转录因子包括WD40重复蛋白透明种皮光滑1(TTG1)、R2R3 MYB转录因子光滑1(GL1)、bHLH转录因子光滑3(GL3)或光滑3增强子(EGL3),以及同源结构域蛋白光滑2(GL2)。包括无毛1(TCL1)、TCL2、三指毛(TRY)、任性(CPC)、TRY和CPC1增强子(ETC1)、ETC2和ETC3在内的R3 MYB转录因子通过与GL1竞争结合GL3或EGL3来负调控表皮毛的形成,从而阻止TTG1 - GL3/EGL3 - GL1(一种激活表皮毛正向调控基因GL2所需的激活复合物)的形成。然而,在其他植物物种尤其是木本植物中,R3 MYB转录因子是否具有类似功能在很大程度上尚不清楚。通过使用拟南芥R3 MYB转录因子TCL1的完整氨基酸序列对毛果杨蛋白质数据库进行BLAST分析,我们在杨树中总共鉴定出8个R3 MYB转录因子基因,即毛果杨无毛1至8(PtrTCL1 - PtrTCL8)。与bHLH转录因子相互作用所需的氨基酸特征以及R3 MYB转录因子细胞间移动所需的氨基酸在所有PtrTCL中并非完全保守。然而,当在拟南芥原生质体中进行测试时,所有PtrTCL都与GL3相互作用。在拟南芥中表达这8个PtrTCL基因中的每一个都会导致无毛表型或表皮毛数量减少的植株,并且在所有测试的转基因植株中GL2的表达水平都大幅降低。在TCL1天然启动子的控制下表达PtrTCL1几乎完全互补了tcl的突变表型。相反,在TRY突变体中TRY天然启动子的控制下或在cpc突变体中CPC天然启动子的控制下表达PtrTCL1会导致无毛表型,这表明PtrTCL1的功能与TCL1相似,但与TRY和CPC不同。