College of Horticulture and Landscape Architecture, Southwest University, Chongqing, 400715, China.
College of Horticulture and Landscape Architecture, Southwest University, Chongqing, 400715, China; School of Life Sciences, Chongqing University, Chongqing, 400045, China.
Biochem Biophys Res Commun. 2019 Oct 8;518(1):148-153. doi: 10.1016/j.bbrc.2019.08.023. Epub 2019 Aug 13.
AGAMOUS-LIKE 24 (AGL24) and AGAMOUS-LIKE 18 (AGL18) are two vital MIKC-type transcription factors to mediate flowering transition in plants. Previous studies indicated that AGL24 acted as an activator but AGL18 served as an inhibitor from vegetative to reproductive growth. However, it is still elusive whether and how AGL24 directly interacts with AGL18 protein. In this study, three homologues of AGL18 (AGL18-1, AGL18-2 and AGL18-3) and AGL24 were cloned in Brassica juncea. Three AGL18 homologues and AGL24 decoded MIKC-type proteins, which were most highly conserved in the M and C domains. AGL18-1, AGL18-2 and AGL18-3 were quite different in the tertiary protein structures. Yeast two-hybrid and pull-down assays showed that AGL18-1, -2 and -3 interacted with AGL24 directly and their K domains of AGL18s were sufficient for their protein interactions. Additionally, mutations in the K domains of AGL18s were costructed and protein interactions were further detected. The results indicated that AGL18-2, AGL18-2, AGL18-2, AGL18-2, AGL18-3, AGL18-3, AGL18-3 and AGL18-3 still interacted with AGL24. However, interestingly, AGL24 interacted with AGL18-1 and AGL18-1 but not AGL18-1. It suggested that the 190th amino acid residue of AGL18-1 played crucial roles in mediating the protein dimerization of AGL18-1/AGL24 in flowering time control.
AGAMOUS-LIKE 24(AGL24)和 AGAMOUS-LIKE 18(AGL18)是两种重要的 MIKC 型转录因子,可介导植物的开花转变。先前的研究表明,AGL24 作为激活剂起作用,而 AGL18 则作为从营养生长到生殖生长的抑制剂。然而,AGL24 是否以及如何直接与 AGL18 蛋白相互作用仍然难以捉摸。在这项研究中,在芸薹属植物中克隆了三个 AGL18 同源物(AGL18-1、AGL18-2 和 AGL18-3)和 AGL24。三个 AGL18 同源物和 AGL24 解码的 MIKC 型蛋白在 M 和 C 结构域中高度保守。AGL18-1、AGL18-2 和 AGL18-3 在三级蛋白质结构上有很大的不同。酵母双杂交和下拉实验表明,AGL18-1、AGL18-2 和 AGL18-3 与 AGL24 直接相互作用,它们的 AGL18s 的 K 结构域足以进行蛋白相互作用。此外,还构建了 AGL18s 的 K 结构域突变体,并进一步检测了蛋白相互作用。结果表明,AGL18-2、AGL18-2、AGL18-2、AGL18-2、AGL18-3、AGL18-3、AGL18-3 和 AGL18-3 仍与 AGL24 相互作用。然而,有趣的是,AGL24 与 AGL18-1 和 AGL18-1 相互作用,但与 AGL18-1 不相互作用。这表明 AGL18-1 的 190 位氨基酸残基在介导 AGL18-1/AGL24 开花时间控制中的蛋白二聚化中起关键作用。