Liang Gang, He Hua, Li Yang, Ai Qin, Yu Diqiu
Key Laboratory of Tropical Forest Ecology, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Kunming, Yunnan 650223, China.
Key Laboratory of Tropical Forest Ecology, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Kunming, Yunnan 650223, China University of Chinese Academy of Sciences, Beijing 100049, China.
J Exp Bot. 2014 Jul;65(12):3215-23. doi: 10.1093/jxb/eru179. Epub 2014 May 6.
Trichome initiation and patterning are controlled by the TTG1-bHLH-MYB regulatory complex. Several MYB transcription factors have been determined to function in trichome development via incorporation into this complex. This study examined the role of MYB82, an R2R3-MYB transcription factor, in Arabidopsis trichome development. MYB82 was revealed to be a nuclear-localized transcription activator. Suppression of MYB82 function by fusion with a dominant repression domain (SRDX) resulted in glabrous leaves, as did overexpression of N-terminal-truncated MYB82. Overexpression of MYB82 genomic sequence, but not its cDNA sequence, led to reduced trichome numbers. Further investigation indicated that at least one of the two introns in MYB82 is essential to the protein's trichome developmental function. An MYB-binding box was identified in the third exon of MYB82, which was inferred to be crucial for MYB82 function because the mutation of this box interfered with the ability of MYB82 to rescue the gl1 mutant. Protein interaction analysis revealed that MYB82 physically interacts with GLABRA3 (GL3). In addition, MYB82 and GL1 can form homodimers and heterodimers at R2R3-MYB domains, which may explain why their overexpression reduces trichome numbers. These results demonstrate the functional diversification of MYB82 and GL1 in trichome development.
表皮毛的起始和模式形成受TTG1-bHLH-MYB调控复合体控制。已确定几种MYB转录因子通过整合到该复合体中在表皮毛发育中发挥作用。本研究检测了R2R3-MYB转录因子MYB82在拟南芥表皮毛发育中的作用。结果显示MYB82是一种定位于细胞核的转录激活因子。与显性抑制结构域(SRDX)融合抑制MYB82功能会导致叶片无毛,N端截短的MYB82过表达也会如此。MYB82基因组序列而非其cDNA序列的过表达导致表皮毛数量减少。进一步研究表明,MYB82中的两个内含子至少有一个对该蛋白在表皮毛发育中的功能至关重要。在MYB82的第三个外显子中鉴定出一个MYB结合框,推测该框对MYB82功能至关重要,因为该框的突变会干扰MYB82拯救gl1突变体的能力。蛋白质相互作用分析表明,MYB82与GLABRA3(GL3)发生物理相互作用。此外,MYB82和GL1可以在R2R3-MYB结构域形成同二聚体和异二聚体,这可能解释了它们的过表达为何会减少表皮毛数量。这些结果证明了MYB82和GL1在表皮毛发育中的功能多样性。