National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Hunan Provincial Key Laboratory of Phytohormones, Hunan Provincial Key Laboratory for Crop Germplasm Innovation and Utilization, College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, China.
Plant Physiol. 2021 Apr 23;185(4):1722-1744. doi: 10.1093/plphys/kiaa121.
Moderate leaf rolling is beneficial for leaf erectness and compact plant architecture. However, our understanding regarding the molecular mechanisms of leaf rolling is still limited. Here, we characterized a semi-dominant rice (Oryza sativa L.) mutant upward rolled leaf 1 (Url1) showing adaxially rolled leaves due to a decrease in the number and size of bulliform cells. Map-based cloning revealed that URL1 encodes the homeodomain-leucine zipper (HD-Zip) IV family member RICE OUTERMOST CELL-SPECIFIC 8 (ROC8). A single-base substitution in one of the two conserved complementary motifs unique to the 3'-untranslated region of this family enhanced URL1 mRNA stability and abundance in the Url1 mutant. URL1 (UPWARD ROLLED LEAF1) contains an ethylene-responsive element binding factor-associated amphiphilic repression motif and functions as a transcriptional repressor via interaction with the TOPLESS co-repressor OsTPL2. Rather than homodimerizing, URL1 heterodimerizes with another HD-ZIP IV member ROC5. URL1 could bind directly to the promoter and suppress the expression of abaxially curled leaf 1 (ACL1), a positive regulator of bulliform cell development. Knockout of OsTPL2 or ROC5 or overexpression of ACL1 in the Url1 mutant partially suppressed the leaf-rolling phenotype. Our results reveal a regulatory network whereby a transcriptional repression complex composed of URL1, ROC5, and the transcriptional corepressor TPL2 suppresses the expression of the ACL1 gene, thus modulating bulliform cell development and leaf rolling in rice.
中度叶片内卷有利于叶片挺立和紧凑的植株结构。然而,我们对于叶片内卷的分子机制的理解仍然有限。在这里,我们描述了一个半显性水稻(Oryza sativa L.)突变体向上卷曲叶 1(Url1),由于泡状细胞数量和大小减少而导致叶片近轴面内卷。基于图谱的克隆表明,URL1 编码同源域-亮氨酸拉链(HD-Zip)IV 家族成员 RICE OUTERMOST CELL-SPECIFIC 8(ROC8)。该家族 3'-非翻译区特有的两个保守互补基序之一的单个碱基取代增强了 Url1 突变体中 URL1 mRNA 的稳定性和丰度。URL1(UPWARD ROLLED LEAF1)含有乙烯反应元件结合因子相关的两亲性抑制基序,通过与 TOPLESS 共抑制子 OsTPL2 相互作用,作为转录抑制剂发挥作用。URL1 不进行同源二聚化,而是与另一个 HD-Zip IV 成员 ROC5 异源二聚化。URL1 可以直接结合到启动子上,并抑制泡状细胞发育的正调控因子 abaxially curled leaf 1(ACL1)的表达。在 Url1 突变体中敲除 OsTPL2 或 ROC5 或过表达 ACL1 部分抑制了叶片内卷表型。我们的结果揭示了一个调控网络,由 URL1、ROC5 和转录核心抑制子 TPL2 组成的转录抑制复合物抑制 ACL1 基因的表达,从而调节水稻泡状细胞的发育和叶片内卷。