Department of Bioenergy Science and Technology and Kumho Life Science Laboratory, Chonnam National University, Gwangju 500-757, Korea.
Plant Cell Physiol. 2013 Oct;54(10):1600-11. doi: 10.1093/pcp/pct105. Epub 2013 Jul 19.
Expansins are non-hydrolytic cell wall-loosening proteins involved in a variety of plant developmental processes during which cell wall modification occurs. Cell wall remodeling proteins including expansins have been suggested to be involved in cell separation to facilitate the emergence of lateral roots (LRs) through the overlaying tissues of the primary root. LBD18/ASL20 activates EXPANSINA14 (EXPA14) expression by directly binding to the EXPA14 promoter to enhance LR emergence in Arabidopsis thaliana. Here we show that EXPA17 is another target gene regulated by LBD18 to promote LR formation in Arabidopsis. We showed that nuclear translocation of the LBD18:GR fusion protein expressed under the Cauliflower mosaic virus (CaMV) 35S promoter or under the LBD18 promoter by dexamethasone treatment results in an increase in EXPA17 transcript levels. β-Glucuronidase (GUS) expression under the EXPA17 promoter, which is detected only in the roots of the wild type, was reduced in the LR primordium and overlaying tissues in an lbd18 mutant background. The number of emerged LRs of the EXPA17 RNAi (RNA interference) Arabidopsis lines was significantly lower than that of the wild type. Overexpression of EXPA17 in Arabidopsis increased the density of emerged LRs in the presence of auxin compared with the wild type. LR induction experiments with a gravitropic stimulus showed that LR emergence is delayed in the EXPA17 RNAi plants compared with the wild type. In addition, EXPA4 expression was also detected in overlaying tissues of the LR primordium and was inducible by LBD18. Taken together, these results support the notion that LBD18 up-regulates a subset of EXP genes to enhance cell separation to promote LR emergence in Arabidopsis.
扩展蛋白是参与各种植物发育过程的非水解细胞壁疏松蛋白,在此过程中细胞壁发生修饰。细胞壁重塑蛋白,包括扩展蛋白,被认为参与细胞分离,以促进侧根(LR)通过主根的覆盖组织出现。LBD18/ASL20 通过直接结合 EXPA14 启动子激活 EXPANSINA14(EXPA14)表达,以增强拟南芥中 LR 的出现。在这里,我们表明 EXPAN17 是另一个受 LBD18 调控的靶基因,以促进拟南芥中 LR 的形成。我们表明,在 Cauliflower mosaic virus (CaMV) 35S 启动子或地塞米松处理下由 LBD18 启动子表达的 LBD18:GR 融合蛋白的核易位导致 EXPA17 转录本水平增加。只有在野生型中才检测到在 EXPA17 启动子下表达的 β-葡萄糖醛酸酶(GUS)表达在 lbd18 突变体背景中的 LR 原基和覆盖组织中减少。EXPA17 RNAi(RNA 干扰)拟南芥系的出现的 LR 数量明显低于野生型。与野生型相比,EXPA17 在拟南芥中的过表达增加了在存在生长素的情况下出现的 LR 的密度。具有向重力刺激的 LR 诱导实验表明,与野生型相比,EXPA17 RNAi 植物的 LR 出现被延迟。此外,还在 LR 原基的覆盖组织中检测到 EXPA4 的表达,并可被 LBD18 诱导。总之,这些结果支持了这样的观点,即 LBD18 上调一组 EXP 基因以增强细胞分离,从而促进拟南芥中 LR 的出现。