Global Protein Interactome Mapping in Rice Using Barcode-Indexed PCR Coupled with HiFi Long-Read Sequencing
文献类型: 外文期刊
第一作者: Liu, Xixi
作者: Liu, Xixi;Luo, Jinjin;Chen, Lijuan;Chen, Yiting;Huang, Jie;Li, Yanan;Xu, Huayu;Yuan, Yang;Cheng, Yu;Li, Zhiyong;Li, Guanghao;Wang, Shiyi;Liu, Xinyong;Liu, Wanning;Zhang, Fengyong;Liu, Zhichao;Tong, Xiaohong;Hou, Yuxuan;Wang, Yifeng;Ying, Jiezheng;Zhang, Jian;Xia, Dandan;Li, Mengyuan;Zhang, Jianwei;Ugli, Abdullaev Mirtemir Baxodir;Ergashev, Mukhammadjon Arabboevich;Zhang, Sanqiang;Yuan, Wenya;Xue, Dawei
作者机构:
关键词: barcode-indexed PCR; HiFi sequencing; protein-protein interactome; rice
期刊名称:ADVANCED SCIENCE ( 影响因子:14.1; 五年影响因子:15.6 )
ISSN:
年卷期: 2025 年 12 卷 11 期
页码:
收录情况: SCI
摘要: Establishing the protein-protein interaction network sheds light on functional genomics studies by providing insights from known counterparts. However, the rice interactome has barely been studied due to the lack of massive, reliable, and cost-effective methodologies. Here, the development of a barcode-indexed PCR coupled with HiFi long-read sequencing pipeline (BIP-seq) is reported for high throughput Protein Protein Interaction (PPI)identification. BIP-seq is essentially built on the integration of library versus library Y2H mating strategy to facilitate the efficient acquisition of random PPI colonies, semi-mechanized dual barcode-indexed yeast colony PCR for the large-scale indexed amplification of bait and prey cDNAs, and massive pac-bio sequencing of PCR amplicon pools. It is demonstrated that BIP-seq could map over 15 000 high-confidence (approximate to 62.5% could be verified by Bimolecular fluorescence Complementation (BiFC)) rice PPIs within 2 months, outperforming the other reported methods. In addition, the obtained 23 032 rice PPIs, including 22,665 newly identified PPIs, greatly expanded the current rice PPI dataset, provided a comprehensive overview of the rice PPIs networks, and could be a valuable asset in facilitating functional genomics research in rice.
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