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PhMYB4 通过 PhC4H 微调矮牵牛的花香挥发物特征。

PhMYB4 fine-tunes the floral volatile signature of Petunia x hybrida through PhC4H.

机构信息

Department of Environmental Horticulture, University of Florida, 1523 Fifield Hall, Gainesville, Florida 32611, USA.

出版信息

J Exp Bot. 2011 Jan;62(3):1133-43. doi: 10.1093/jxb/erq342. Epub 2010 Nov 10.

DOI:10.1093/jxb/erq342
PMID:21068208
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3022401/
Abstract

In Petunia × hybrida cv 'Mitchell Diploid' (MD), floral volatile benzenoid/phenylpropanoid (FVBP) biosynthesis is controlled spatially, developmentally, and daily at molecular, metabolic, and biochemical levels. Multiple genes have been shown to encode proteins that either directly catalyse a biochemical reaction yielding FVBP compounds or are involved in metabolite flux prior to the formation of FVBP compounds. It was hypothesized that multiple transcription factors are involved in the precise regulation of all necessary genes, resulting in the specific volatile signature of MD flowers. After acquiring all available petunia transcript sequences with homology to Arabidopsis thaliana R2R3-MYB transcription factors, PhMYB4 (named for its close identity to AtMYB4) was identified, cloned, and characterized. PhMYB4 transcripts accumulate to relatively high levels in floral tissues at anthesis and throughout open flower stages, which coincides with the spatial and developmental distribution of FVBP production and emission. Upon RNAi suppression of PhMYB4 (ir-PhMYB4) both petunia cinnamate-4-hydroxylase (PhC4H1 and PhC4H2) gene transcript levels were significantly increased. In addition, ir-PhMYB4 plants emit higher levels of FVBP compounds derived from p-coumaric acid (isoeugenol and eugenol) compared with MD. Together, these results indicate that PhMYB4 functions in the repression of C4H transcription, indirectly controlling the balance of FVBP production in petunia floral tissue (i.e. fine-tunes).

摘要

在杂种矮牵牛 cv 'Mitchell Diploid'(MD)中,花香苯丙烷类(FVBP)生物合成在分子、代谢和生化水平上在空间、发育和日常水平上受到控制。已经表明,多个基因编码的蛋白质要么直接催化产生 FVBP 化合物的生化反应,要么参与 FVBP 化合物形成之前的代谢物通量。假设多个转录因子参与所有必需基因的精确调控,从而导致 MD 花朵的特定挥发性特征。在获得与拟南芥 R2R3-MYB 转录因子具有同源性的所有可用矮牵牛转录序列后,鉴定、克隆和表征了 PhMYB4(因其与 AtMYB4 非常相似而得名)。PhMYB4 转录本在开花期和整个开花阶段在花组织中积累到相对较高的水平,这与 FVBP 产生和释放的空间和发育分布一致。在用 PhMYB4 的 RNAi 抑制(ir-PhMYB4)后,PhC4H1 和 PhC4H2 的基因转录本水平显著增加。此外,与 MD 相比,ir-PhMYB4 植物会释放出更高水平的源自对香豆酸的 FVBP 化合物(异丁香酚和丁香酚)。这些结果表明 PhMYB4 可抑制 C4H 转录,间接控制矮牵牛花组织中 FVBP 产生的平衡(即微调)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/beabd68e0631/jexboterq342f06_3c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/9af524b4e98f/jexboterq342f01_3c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/b85a6d561e78/jexboterq342f02_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/fcca94cc7322/jexboterq342f03_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/fab70b16e7ad/jexboterq342f04_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/ecf7ae4dcabb/jexboterq342f05_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/beabd68e0631/jexboterq342f06_3c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/9af524b4e98f/jexboterq342f01_3c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/b85a6d561e78/jexboterq342f02_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/fcca94cc7322/jexboterq342f03_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/fab70b16e7ad/jexboterq342f04_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/ecf7ae4dcabb/jexboterq342f05_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a5/3022401/beabd68e0631/jexboterq342f06_3c.jpg

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