作者
Haigang Yan,Yulong Ren,Binglei Zhang,Jie Jin,Feilong Du,Zhuangzhuang Shan,Yushuang Fu,Yun Zhu,Xin Wang,Changyuan Zhu,Yue Cai,Jie Zhang,Li Wang,Xiao Zhang,Rongqi Wang,Li Wang,Hancong Xu,Ling Jiang,Xi Liu,Shanshan Zhu,Qibing Lin,Cailin Lei,Zhijun Cheng,Yihua Wang,Wenwei Zhang,Jianmin Wan
摘要
Summary Starch is synthesized as insoluble, semicrystalline particles within plant chloroplast and amyloplast, which are referred to as starch grains (SGs). The size and morphology of SGs in the cereal endosperm are diverse and species–specific, representing a key determinant of the suitability of starch for industrial applications. However, the molecular mechanisms modulating SG size in cereal endosperm remain elusive. Here, we functionally characterized the rice ( Oryza sativa ) mutant substandard starch grain7 ( ssg7 ), which exhibits enlarged SGs and defective endosperm development. SSG7 encodes a plant–specific DUF1001 domain‐containing protein homologous to Arabidopsis ( Arabidopsis thaliana ) CRUMPLED LEAF (AtCRL). SSG7 localizes to the amyloplast membrane in developing endosperm. Several lines of evidence suggest that SSG7 functions together with SSG4 and SSG6, known as two regulators essential for SG development, to control SG size, by interacting with translocon‐associated components, which unveils a molecular link between SG development and protein import. Genetically, SSG7 acts synergistically with SSG4 and appears to be functional redundancy with SSG6 in modulating SG size and endosperm development. Collectively, our findings uncover a multimeric functional protein complex involved in SG development in rice. SSG7 represents a promising target gene for the biotechnological modification of SG size, particularly for breeding programs aimed at improving starch quality.