1. Comprehensive proteomic analysis of developing protein bodies in maize (Zea mays) endosperm provides novel insights into its biogenesis
- Author
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Dongsheng Yao, Gang Wang, Han Liang, Jiajia Wang, Guifeng Wang, Yulong Du, Bilian Shuai, Yuanping Tang, and Rentao Song
- Subjects
Proteomics ,protein body ,0106 biological sciences ,0301 basic medicine ,Physiology ,Zein ,Plant Science ,Endoplasmic Reticulum ,Zea mays ,01 natural sciences ,Endosperm ,03 medical and health sciences ,Botany ,Storage protein ,Prolamin ,proteomic ,chemistry.chemical_classification ,biology ,Endoplasmic reticulum ,Seed Storage Proteins ,food and beverages ,storage protein ,Cell biology ,030104 developmental biology ,chemistry ,Protein body ,Plant protein ,Proteome ,biology.protein ,Ribosomes ,prolamin ,Metabolic Networks and Pathways ,Research Paper ,010606 plant biology & botany - Abstract
Highlight Proteomic analysis of developing maize protein bodies (PBs) reveals an unexpected diversity and complexity of PB proteins, and provides a roadmap for the transport and translation of mRNAs of zein genes, and the assembly of PBs., Prolamins, the major cereal seed storage proteins, are sequestered and accumulated in the lumen of the endoplasmic reticulum (ER), and are directly assembled into protein bodies (PBs). The content and composition of prolamins are the key determinants for protein quality and texture-related traits of the grain. Concomitantly, the PB-inducing fusion system provides an efficient target to produce therapeutic and industrial products in plants. However, the proteome of the native PB and the detailed mechanisms underlying its formation still need to be determined. We developed a method to isolate highly purified and intact PBs from developing maize endosperm and conducted proteomic analysis of intact PBs of zein, a class of prolamine protein found in maize. We thus identified 1756 proteins, which fall into five major categories: metabolic pathways, response to stimulus, transport, development, and growth, as well as regulation. By comparing the proteomes of crude and enriched extractions of PBs, we found substantial evidence for the following conclusions: (i) ribosomes, ER membranes, and the cytoskeleton are tightly associated with zein PBs, which form the peripheral border; (ii) zein RNAs are probably transported and localized to the PB–ER subdomain; and (iii) ER chaperones are essential for zein folding, quality control, and assembly into PBs. We futher confirmed that OPAQUE1 (O1) cannot directly interact with FLOURY1 (FL1) in yeast, suggesting that the interaction between myosins XI and DUF593-containing proteins is isoform-specific. This study provides a proteomic roadmap for dissecting zein PB biogenesis and reveals an unexpected diversity and complexity of proteins in PBs.
- Published
- 2016
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