Shin Dong Ho, Cho Misuk, Choi Myoung Goo, Das Prasanta Kumar, Lee Seul-Ki, Choi Sang-Bong, Park Youn-Il
Department of Biological Sciences, Chungnam National University, 99 Daehagro, Youseong, Daejeon, 305-764, Korea.
Plant Cell Rep. 2015 May;34(5):805-15. doi: 10.1007/s00299-015-1743-7. Epub 2015 Jan 21.
A putative RNA-binding protein with a single RNA Recognition Motif (At3G63450) is involved in anthocyanin biosynthesis via its ability to modulate the transcript level of a major positive regulator PAP1 in Arabidopsis. The R2R3 MYB-activator production of anthocyanin pigment 1 (PAP1)/MYB75 plays a major role in anthocyanin biosynthesis in Arabidopsis in combination with one of three bHLH activators including transparent test 8 (TT8), enhancer of glabra3 (EGL3), glabra3 (GL3), and the WD-repeat transcription factor transparent testa 1 (TTG1), forming ternary MYB-basic HLH-WD40 complexes. Transcriptional activation of PAP1 expression is largely triggered by changes in light color and intensity, temperature fluctuations, nutrient status, and sugar and hormone treatments. However, the immediate upstream and downstream regulatory factors for PAP1 transcription are largely unknown. In the present study, using a T-DNA insertional mutagenesis approach, we transformed pap1-Dominant (pap1D) plants to modulate the levels of endogenous PAP1 transcripts. We employed Restriction Site Extension (RSE)-PCR analysis of 247 homogenous T3 genetic mutant lines exhibiting variations in anthocyanin accumulation compared to pap1D and identified 92 lines with T-DNA integrated in either intra- or inter-genic locations. This analysis revealed 80 novel candidate proteins, including a putative RNA-binding protein with a single RNA Recognition Motif (At3G63450), which may directly or indirectly regulate PAP1 expression at the transcriptional level.
一种具有单个RNA识别基序的假定RNA结合蛋白(At3G63450)通过调节拟南芥中主要正调控因子PAP1的转录水平参与花青素生物合成。花青素色素1(PAP1)/MYB75的R2R3 MYB激活剂的产生与三种bHLH激活剂之一(包括透明 testa 8(TT8)、glabra3增强子(EGL3)、glabra3(GL3))以及WD重复转录因子透明 testa 1(TTG1)结合,在拟南芥花青素生物合成中起主要作用,形成三元MYB-碱性HLH-WD40复合物。PAP1表达的转录激活主要由光的颜色和强度变化、温度波动、营养状况以及糖和激素处理触发。然而,PAP1转录的直接上游和下游调控因子在很大程度上尚不清楚。在本研究中,我们使用T-DNA插入诱变方法转化pap1-Dominant(pap1D)植物,以调节内源性PAP1转录本的水平。我们对247个与pap1D相比花青素积累表现出差异的同质T3遗传突变系进行了限制性位点延伸(RSE)-PCR分析,并鉴定出92个T-DNA整合在基因内或基因间位置的品系。该分析揭示了80种新的候选蛋白,包括一种具有单个RNA识别基序的假定RNA结合蛋白(At3G63450),其可能在转录水平直接或间接调节PAP1表达。