番茄果实的蛋白质组学和磷酸化蛋白质组学鉴定叶绿体覆盖减少1a是成熟调节因子。

IF 7.9
Jinjuan Tan, Zhongjing Zhou, Hanqian Feng, Jiateng Zhang, Ruikai Zhang, Zhongkai Chen, Yujie Niu, Fangyu Liu, Zhiping Deng
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引用次数: 0

摘要

在转录组学水平上对番茄果实成熟进行了广泛的研究。然而,对番茄果实蛋白质组和磷蛋白质组的全面分析仍然有限。在这项研究中,我们使用基于串联质量标签(TMT)的定量蛋白质组学对番茄(Ailsa Craig)果实在五个成熟阶段进行了大规模蛋白质组学和磷酸化蛋白质组学分析。我们的分析量化了超过8800个蛋白质和20,000个高可信度的磷酸化位点。成熟相关的磷酸化和去磷酸化事件在多种成熟调节因子中被发现,包括转录因子、乙烯生物合成和信号蛋白,以及表观遗传修饰因子。加权基因共表达网络分析(WGCNA)揭示了一个四肽重复蛋白,即减少叶绿体覆盖1a (REC1a),是果实成熟的关键调控因子。基于平行反应监测(PRM)的靶向蛋白质组学分析验证了REC1a及其三个磷酸化位点的表达谱。聚集规律间隔短回复性重复序列(CRISPR)-CRISPR相关蛋白9 (Cas9)介导的REC1a基因敲除导致番茄红素积累减少和叶绿素降解减慢,突出了其在叶绿体向染色质转变中的作用,这对成熟过程中果实色素沉着至关重要。rec1a突变体的定量蛋白质组学分析表明,Clp蛋白酶和伴侣蛋白(已知的调节质体转变的蛋白质)水平降低。此外,共免疫沉淀和分裂荧光素酶互补实验显示,REC1a与真核翻译起始因子亚基eIF2α和eIF2Bβ相互作用,提示其在成熟过程中调节蛋白质合成。该研究提供了迄今为止最全面的番茄果实定量蛋白质组和磷酸化蛋白质组图谱,并确定了REC1a是一种新的质体发育调节因子,为研究果实成熟的分子机制提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proteome and Phosphoproteome of Tomato Fruit Identify REDUCED CHLOROPLAST COVERAGE 1a as A Ripening Regulator.

Fruit ripening in tomato (Solanum lycopersicum) has been extensively studied at the transcriptomics level. However, comprehensive profiling of the tomato fruit proteome and phosphoproteome remains limited. In this study, we performed large-scale proteome and phosphoproteome profiling of tomato (Ailsa Craig) fruits across five ripening stages using tandem mass tags (TMT)-based quantitative proteomics. Our analysis quantified over 8800 proteins and 20,000 high-confidence phosphorylation sites. Ripening-associated phosphorylation and dephosphorylation events were identified in diverse ripening regulators, including transcription factors, ethylene biosynthesis and signaling proteins, and epigenetic modifiers. Weighted gene co-expression network analysis (WGCNA) revealed a tetratricopeptide repeat protein, REDUCED CHLOROPLAST COVERAGE 1a (REC1a), as a key regulator of fruit ripening. Parallel reaction monitoring (PRM)-based targeted proteomic analysis validated the expression profiles of REC1a and its three phosphorylation sites. Clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein 9 (Cas9)-mediated knockout of REC1a resulted in reduced lycopene accumulation and slower chlorophyll degradation, highlighting its role in the chloroplast-to-chromoplast transition, which is critical for fruit pigmentation during ripening. Quantitative proteomic analyses of rec1a mutants demonstrated reduced levels of Clp proteases and chaperones, proteins known to regulate plastid transitions. Additionally, co-immunoprecipitation and split-luciferase complementation assays revealed that REC1a interacts with the eukaryotic translation initiation factor subunits eIF2α and eIF2Bβ, suggesting its role in regulating protein synthesis during ripening. This study provides the most comprehensive quantitative proteome and phosphoproteome atlas of tomato fruits to date and identifies REC1a as a novel regulator of plastid development, offering new insights into the molecular mechanisms underlying fruit ripening.

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