Han Yuliang, Zhang Juncheng, Zhang Siqi, Xiang Lijun, Lei Zhonghua, Huang Qixiu, Wang Huizhong, Chen Tao, Cai Maohong
Zhejiang Provincial Key Laboratory for Genetic Improvement and Quality Control of Medicinal Plants, College of Life and Environmental Science, Hangzhou Normal University, Hangzhou, China.
Institute of Economic Crops, Xinjiang Academy of Agricultural Sciences, China.
Physiol Plant. 2024 Mar-Apr;176(2):e14286. doi: 10.1111/ppl.14286.
Shoot branching fundamentally influences plant architecture and agricultural yield. However, research on shoot branching in Dendrobium catenatum, an endangered medicinal plant in China, remains limited. In this study, we identified a transcription factor DcERF109 as a key player in shoot branching by regulating the expression of strigolactone (SL) receptors DWARF 14 (D14)/ DECREASED APICAL DOMINANCE 2 (DAD2). The treatment of D. catenatum seedlings with GR24/TIS108 revealed that SL can significantly repress the shoot branching in D. catenatum. The expression of DcERF109 in multi-branched seedlings is significantly higher than that of single-branched seedlings. Ectopic expression in Arabidopsis thaliana demonstrated that overexpression of DcERF109 resulted in significant shoot branches increasing and dwarfing. Molecular and biochemical assays demonstrated that DcERF109 can directly bind to the promoters of AtD14 and DcDAD2.2 to inhibit their expression, thereby positively regulating shoot branching. Inhibition of DcERF109 by virus-induced gene silencing (VIGS) resulted in decreased shoot branching and improved DcDAD2.2 expression. Moreover, overexpression of DpERF109 in A. thaliana, the homologous gene of DcERF109 in Dendrobium primulinum, showed similar phenotypes to DcERF109 in shoot branch and plant height. Collectively, these findings shed new insights into the regulation of plant shoot branching and provide a theoretical basis for improving the yield of D. catenatum.
茎分枝从根本上影响植物形态和农业产量。然而,对于中国濒危药用植物铁皮石斛茎分枝的研究仍然有限。在本研究中,我们鉴定出一个转录因子DcERF109,它通过调控独脚金内酯(SL)受体DWARF 14(D14)/ DECREASED APICAL DOMINANCE 2(DAD2)的表达,在茎分枝中起关键作用。用GR24/TIS108处理铁皮石斛幼苗表明,SL能显著抑制铁皮石斛的茎分枝。多分枝幼苗中DcERF109的表达显著高于单分枝幼苗。在拟南芥中的异位表达表明,DcERF109的过表达导致茎分枝显著增加和植株矮化。分子和生化分析表明,DcERF109可直接结合AtD14和DcDAD2.2的启动子以抑制它们的表达,从而正向调控茎分枝。通过病毒诱导基因沉默(VIGS)抑制DcERF109导致茎分枝减少和DcDAD2.2表达增加。此外,在报春石斛中DcERF109的同源基因DpERF109在拟南芥中的过表达在茎分枝和株高方面表现出与DcERF109相似的表型。总的来说,这些发现为植物茎分枝调控提供了新的见解,并为提高铁皮石斛产量提供了理论依据。