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芒果(L.)基因的分离与功能鉴定。

Isolation and Functional Characterization of a Gene in Mango ( L.).

机构信息

State Key Laboratory for the Conservation and Utilization of Subtropical Agro-Bioresources, College of Agriculture, Guangxi University, 100 East Daxue Road, Nanning 530004, China.

出版信息

Int J Mol Sci. 2022 Apr 2;23(7):3974. doi: 10.3390/ijms23073974.

Abstract

() plays an important role in the flowering process of plants, controlling flowering time and mediating floral meristem differentiation. Owing to its considerable importance, the mango gene (; GenBank accession no. HQ585988) was isolated, and its expression pattern and function were characterized in the present study. The cDNA sequence of was 1152 bp, and it encoded a 383 amino acid protein. was expressed in all tested tissues and was highly expressed in flowers and buds. Temporal expression analysis showed that expression was correlated with floral development stage, and two relative expression peaks were detected in the early stages of floral transition and floral organ differentiation. Moreover, 35S::GFP-MiLFY fusion protein was shown to be localized to the nucleus of cells. Overexpression of in promoted early flowering and the conversion of lateral meristems into terminal flowers. In addition, transgenic plants exhibited obvious morphological changes, such as differences in cauline leaf shape, and the number of lateral branches. When driven by the promoter, was highly expressed in leaves, floral organs, stems, and roots, during the flowering period. Exogenous gibberellin (GA) treatment downregulated promoter expression, but paclobutrazol (PPP) upregulated it. Bimolecular fluorescence complementation (BiFC) assays showed that the MiLFY protein can interact with zinc-finger protein 4 (ZFP4) and SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (MiSOC1D). Taken together, these results indicate that plays a pivotal role in controlling mango flowering, and that it is regulated by gibberellin and paclobutrazol.

摘要

() 在植物的开花过程中起着重要作用,控制开花时间并介导花分生组织的分化。由于其重要性,本研究分离了芒果 () 基因(GenBank 登录号 HQ585988),并对其表达模式和功能进行了表征。的 cDNA 序列长 1152bp,编码一个 383 个氨基酸的蛋白质。在所有测试的组织中都表达了,在花和芽中表达量较高。时间表达分析表明,与花发育阶段相关,在花转变和花器官分化的早期阶段检测到两个相对表达高峰。此外,35S::GFP-MiLFY 融合蛋白被证明定位于细胞的细胞核。在 中过表达促进了早期开花和侧芽向顶芽的转化。此外,转基因植物表现出明显的形态变化,如茎生叶形状和侧枝数量的差异。当由 启动子时,在开花期在叶片、花器官、茎和根中高度表达。外源赤霉素(GA)处理下调 启动子的表达,但多效唑(PPP)上调其表达。双分子荧光互补(BiFC)试验表明,MiLFY 蛋白可以与锌指蛋白 4(ZFP4)和 CONSTANS1 的抑制物(MiSOC1D)相互作用。总之,这些结果表明在控制芒果开花中起着关键作用,并且受赤霉素和多效唑的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce2c/9000169/5bc6343a0318/ijms-23-03974-g001.jpg

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