Lee Areum, Lee Sang Sook, Jung Won Yong, Park Hyun Ji, Lim Bo Ra, Kim Hyun-Soon, Ahn Jun Cheul, Cho Hye Sun
Biosystems and Bioengineering Program, University of Science and Technology (UST), Daejeon 34113, Korea.
Molecular Biofarming Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 34141, Korea.
Int J Mol Sci. 2016 Jul 19;17(7):1154. doi: 10.3390/ijms17071154.
Alternative splicing (AS) is an important molecular mechanism by which single genes can generate multiple mRNA isoforms. We reported previously that, in Oryza sativa, the cyclophilin 19-4 (OsCYP19-4.1) transcript was significantly upregulated in response to cold stress, and that transgenic plants were cold tolerant. Here we show that, under cold stress, OsCYP19-4 produces eight transcript variants by intron retention and exon skipping, resulting in production of four distinct protein isoforms. The OsCYP19-4 AS isoforms exhibited different cellular localizations in the epidermal cells: in contrast to OsCYP19-4.1, the OsCYP19-4.2 and OsCYP19-4.3 proteins were primarily targeted to guard and subsidiary cells, whereas OsCYP19-4.5, which consists largely of an endoplasmic reticulum (ER) targeting signal, was co-localized with the RFP-BiP marker in the ER. In OsCYP19-4.2, the key residues of the PPIase domain are altered; consistent with this, recombinant OsCYP19-4.2 had significantly lower PPIase activity than OsCYP19-4.1 in vitro. Specific protein-protein interactions between OsCYP19-4.2/3 and AtRCN1 were verified in yeast two-hybrid (Y2H) and bimolecular fluoresence complementation (BiFC assays), although the OsCYP19-4 isoforms could not bind each other. Based on these results, we propose that two OsCYP19-4 AS isoforms, OsCYP19-4.2 and OsCYP19-4.3, play roles linking auxin transport and cold stress via interactions with RCN1.
可变剪接(AS)是一种重要的分子机制,通过该机制单个基因可以产生多种mRNA异构体。我们之前报道过,在水稻中,亲环蛋白19-4(OsCYP19-4.1)转录本在冷胁迫下显著上调,并且转基因植物具有耐寒性。在此我们表明,在冷胁迫下,OsCYP19-4通过内含子保留和外显子跳跃产生8种转录变体,从而产生4种不同的蛋白质异构体。OsCYP19-4可变剪接异构体在表皮细胞中表现出不同的细胞定位:与OsCYP19-4.1不同,OsCYP19-4.2和OsCYP19-4.3蛋白主要定位于保卫细胞和副卫细胞,而主要由内质网(ER)靶向信号组成的OsCYP19-4.5与ER中的RFP-BiP标记共定位。在OsCYP19-4.2中,肽脯氨酰顺反异构酶(PPIase)结构域的关键残基发生了改变;与此一致的是,重组OsCYP19-4.2在体外的PPIase活性明显低于OsCYP19-4.1。尽管OsCYP19-4异构体之间不能相互结合,但在酵母双杂交(Y2H)和双分子荧光互补(BiFC)试验中验证了OsCYP19-4.2/3与AtRCN1之间存在特异性蛋白质-蛋白质相互作用。基于这些结果,我们提出两种OsCYP19-4可变剪接异构体OsCYP19-4.2和OsCYP19-4.3通过与RCN1相互作用在连接生长素运输和冷胁迫方面发挥作用。