五三肽重复
生物发生
基因敲除
生物
RNA剪接
第二组内含子
突变体
内含子
质体
遗传学
拟南芥
选择性拼接
基因
叶绿体
核糖核酸
拟南芥
细胞生物学
RNA结合蛋白
信使核糖核酸
作者
Li Zhang,Jingli Chen,Liqun Zhang,Ying Wei,Yajuan Li,Xinyun Xu,Hui Wu,Zhong‐Nan Yang,Jirong Huang,Fenhong Hu,Weihua Huang,Yong‐Lan Cui
摘要
ABSTRACT Chloroplast biogenesis requires the coordinated expression of chloroplast and nuclear genes. Here, we show that EMB1270, a plastid‐localized pentatricopeptide repeat (PPR) protein, is required for chloroplast biogenesis in Arabidopsis thaliana . Knockout of EMB1270 led to embryo arrest, whereas a mild knockdown mutant of EMB1270 displayed a virescent phenotype. Almost no photosynthetic proteins accumulated in the albino emb1270 knockout mutant. By contrast, in the emb1270 knockdown mutant, the levels of ClpP1 and photosystem I (PSI) subunits were significantly reduced, whereas the levels of photosystem II (PSII) subunits were normal. Furthermore, the splicing efficiencies of the clpP1.2 , ycf3.1 , ndhA , and ndhB plastid introns were dramatically reduced in both emb1270 mutants. RNA immunoprecipitation revealed that EMB1270 associated with these introns in vivo . In an RNA electrophoretic mobility shift assay (REMSA), a truncated EMB1270 protein containing the 11 N‐terminal PPR motifs bound to the predicted sequences of the clpP1.2 , ycf3.1 , and ndhA introns. In addition, EMB1270 specifically interacted with CRM Family Member 2 (CFM2). Given that CFM2 is known to be required for splicing the same plastid RNAs, our results suggest that EMB1270 associates with CFM2 to facilitate the splicing of specific group II introns in Arabidopsis .
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