State Key Laboratory of Plant Physiology and Biochemistry, College of Life Sciences, Zhejiang University, Hangzhou 310058, China.
College of Bioscience and Biotechnology, Yangzhou University, Yangzhou 225009, China.
Plant Cell. 2019 Jun;31(6):1257-1275. doi: 10.1105/tpc.19.00038. Epub 2019 Apr 2.
The major root system of cereals consists of crown roots (or adventitious roots), which are important for anchoring plants in the soil and for water and nutrient uptake. However, the molecular basis of crown root formation is largely unknown. Here, we isolated a rice () mutant with fewer crown roots, named (). Map-based cloning revealed that is caused by a mutation of a putative transcription factor-coding gene, (). We demonstrate that the point mutation in perturbs the microRNA156 (OsmiR156)-directed cleavage of transcripts, resulting in the mutant phenotype. Chromatin immunoprecipitation sequencing assays of OsSPL3 binding sites and RNA sequencing of differentially expressed transcripts in further identified potential direct targets of OsSPL3 in basal nodes, including a MADS-box transcription factor, OsMADS50. overexpressing plants produced fewer crown roots, phenocopying , while knocking out in the background reversed this phenotype. We also show that , another OsmiR156 target gene, regulates and crown root development. Taken together, our findings suggest a novel regulatory pathway in which the OsmiR156- module directly activates in the node to regulate crown root development in rice.
主要的禾本科植物根系由冠根(或不定根)组成,冠根对于植物在土壤中的固定和水分及养分的吸收非常重要。然而,冠根形成的分子基础在很大程度上是未知的。在这里,我们分离到一个水稻突变体,其冠根较少,命名为 ()。基于图谱的克隆表明,是由一个假定的转录因子编码基因的突变引起的,该基因名为 ()。我们证明,中一个点突变扰乱了 microRNA156(OsmiR156)对 转录本的靶向切割,导致了突变表型。OsSPL3 结合位点的染色质免疫沉淀测序分析和 中差异表达转录本的 RNA 测序进一步鉴定了 OsSPL3 在基部节点的潜在直接靶标,包括一个 MADS 框转录因子 OsMADS50。过表达植株产生的冠根较少,表型与 相似,而在 背景中敲除 则逆转了这种表型。我们还表明,另一个 OsmiR156 靶基因 ,调节 并影响冠根发育。总之,我们的研究结果表明,在水稻中,OsmiR156 模块通过直接激活节点中的 来调节冠根发育,这是一个新的调控途径。