| Literature DB >> 33716298 |
Wenfang Zeng1, Liang Niu1, Zhaohui Wang2, Xiaobei Wang1, Yan Wang1, Lei Pan1, Zhenhua Lu1, Guochao Cui1, Weining Weng2, Mingqiao Wang2, Xun Meng3,4, Zhiqiang Wang5.
Abstract
Peach (Prunus persica) is a typical climacteric fruit that produces ethylene rapidly during ripening, and its fruit softens quickly. Stony hard peach cultivars, however, do not produce large amounts of ethylene, and the fruit remains firm until fully ripe, thus differing from melting flesh peach cultivars. To identify the key proteins involved in peach fruit ripening, an antibody-based proteomic analysis was conducted. A mega-monoclonal antibody (mAb) library was generated and arrayed on a chip (mAbArray) at a high density, covering ~4950 different proteins of peach. Through the screening of peach fruit proteins with the mAbArray chip, differentially expressed proteins recognized by 1587 mAbs were identified, and 33 corresponding antigens were ultimately identified by immunoprecipitation and mass spectrometry. These proteins included not only important enzymes involved in ethylene biosynthesis, such as ACO1, SAHH, SAMS, and MetE, but also novel factors such as NUDT2. Furthermore, protein-protein interaction analysis identified a metabolon containing SAHH and MetE. By combining the antibody-based proteomic data with the transcriptomic and metabolic data, a mathematical model of ethylene biosynthesis in peach was constructed. Simulation results showed that MetE is an important regulator during peach ripening, partially through interaction with SAHH.Year: 2020 PMID: 33716298 DOI: 10.1038/s41438-020-0249-9
Source DB: PubMed Journal: Hortic Res ISSN: 2052-7276 Impact factor: 6.793