School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027, China.
School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027, China
J Exp Bot. 2014 Aug;65(15):4285-95. doi: 10.1093/jxb/eru202. Epub 2014 May 12.
The gain-of-function mutant edt1 shows significantly enhanced drought tolerance and a well-developed root system including deeper primary roots and more lateral roots. To explore the molecular mechanisms underlying the improved root system of edt1, we performed transcriptome comparison between the wild-type and edt1 roots. One of the interesting findings from the analysis was that several gene families of cell-wall-loosening proteins were upregulated in the mutant roots, including expansins, extensins, xyloglucan endotransglucosylase/hydrolases (XTHs), pectin-related enzymes, and cellulases. Most of these genes contain HD-binding cis-elements in their promoters predominantly with the TTTAATTT sequence, which can be bound by HDG11 in vitro and in vivo. The coordinated expression of these gene families overlaps fast root elongation. Furthermore, overexpression of AtEXPA5, which was dramatically upregulated in edt1, resulted in longer primary roots because cells were more extended longitudinally. When combined by crossing the AtEXPA5-overexpression lines with one pectin methylesterase inhibitor family protein (PMEI) gene (At5g62360)- or one cellulase (CEL) gene (At2g32990)-overexpression lines, the primary roots of the progeny even exceeded both parents in length. Our results demonstrate that HDG11 directly upregulates cell-wall-loosening protein genes, which is correlated with altered root system architecture, and confirm that cell-wall-loosening proteins play important roles in coordinating cell-wall extensibility with root development. The results of transgene experiments showed that expansin works together with PMEI and CEL to generate synergistic effects on primary root elongation, suggesting that different cell-wall-loosening protein families may function in combination to generate optimal effects on root extensibility.
功能获得型突变体 edt1 表现出显著增强的耐旱性和发育良好的根系,包括更深的主根和更多的侧根。为了探索 edt1 根系改善的分子机制,我们对野生型和 edt1 根系进行了转录组比较。分析中的一个有趣发现是,突变体根中几个细胞壁松弛蛋白基因家族上调,包括扩展蛋白、伸展蛋白、木葡聚糖内转糖苷酶/水解酶 (XTHs)、果胶相关酶和纤维素酶。这些基因中的大多数在其启动子中含有 HD 结合顺式元件,主要是 TTTAATTT 序列,该序列可以在体外和体内与 HDG11 结合。这些基因家族的协调表达与快速根伸长重叠。此外,AtEXPA5 的过表达,其在 edt1 中显著上调,导致主根变长,因为细胞纵向更伸展。当将 AtEXPA5 过表达系与一个果胶甲酯酶抑制剂家族蛋白 (At5g62360) 或一个纤维素酶 (At2g32990) 过表达系杂交时,后代的主根长度甚至超过了双亲。我们的结果表明,HDG11 直接上调细胞壁松弛蛋白基因,这与改变的根系结构相关,并证实细胞壁松弛蛋白在协调细胞壁伸展性与根系发育方面发挥重要作用。转基因实验的结果表明,扩展蛋白与 PMEI 和 CEL 一起协同作用于主根伸长,表明不同的细胞壁松弛蛋白家族可能以组合的方式发挥作用,以对根的伸展性产生最佳效果。