RNA剪接
内含子
生物发生
生物
第二组内含子
外显子剪接增强剂
遗传学
叶绿体
细胞生物学
SR蛋白
拼接因子
核糖核酸
RNA解旋酶A
基因
RNA结合蛋白
小剪接体
选择性拼接
核糖核蛋白
拟南芥
功能(生物学)
叶绿体DNA
作者
Chu Zeng,Qingsong Jiao,Xuan Zhao,Ting Jia,Xueyun Hu
标识
DOI:10.1093/plphys/kiag014
摘要
ACCUMULATION OF PHOTOSYSTEM ONE2 (APO2) is an essential protein for embryo development, yet its functional role remains largely unexplored. In this study, we generated inducible APO2 RNA interference (RNAi) lines to investigate the function of APO2. Upon induction, APO2-RNAi plants exhibited a yellow phenotype in newly emerging leaves, accompanied by defective chloroplast development. We demonstrated that APO2 localizes to chloroplasts and that APO2 is highly expressed in green leaves. Phylogenetic analysis of the APO protein family across land plants revealed that APO2 proteins cluster into a distinct clade separate from other APO family members. The splicing of several chloroplast introns was affected in APO2-RNAi-induced yellow leaves, with splicing efficiencies of the ycf3.1 and ndhA introns dramatically lower than those in green leaves. We determined that APO2 interacts with two splicing factors, chloroplast RNA splicing 2-associated Factor 1 (CAF1)/CAF2 and DEAD-box RNA helicase 3 (RH3), which are involved in group II intron splicing. Our results also revealed splicing deficiencies in both ycf3.1 and ndhA introns in RH3 cosuppression lines. Notably, both APO2 and RH3 directly bound the 5' region of ycf3.1. These results establish that APO2 is indispensable for chloroplast biogenesis, primarily due to its essential role in the splicing of chloroplast introns.
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