综合多组学分析揭示了植物寄生线虫(Meloidogyne incognita)的翻译景观。

IF 5.8 1区 生物学 Q1 BIOLOGY Communications Biology Pub Date : 2025-01-28 DOI:10.1038/s42003-025-07533-x
Zhaolu Zhu, Dexin Bo, Chuanshuai Xie, Dadong Dai, Donghai Peng, Ming Sun, Jinshui Zheng
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引用次数: 0

摘要

根结线虫(rootknot nematdes, RKNs)作为植物寄生线虫具有破坏性,对全球粮食安全构成最严重的威胁。尽管对RKNs基因转录谱的研究得到了极大的关注,但我们对RKNs翻译前景的理解仍然有限。在这项研究中,我们通过翻译组、转录组和定量蛋白质组分析的整合,阐明了Meloidogyne incognita的翻译景观。我们的发现揭示了许多以前未注释的翻译事件,并改进了基因组注释。通过对寄生蜂寄生过程中全基因组翻译动态的研究,我们发现寄生蜂的基因在翻译水平上受到寄生期特异性调控。有趣的是,我们确定了470个微肽(含有少于100个氨基酸)具有潜在的效应物功能。此外,我们还观察到,在M. incognita中,效应编码基因表现出更高的翻译效率(TE)。进一步的分析表明,M. incognita有可能调节效应编码基因的TE,而不会同时改变其转录物的丰度,从而促进效应合成。总的来说,我们的研究提供了全面的数据集,并探索了incognita的全基因组翻译景观,揭示了寄生过程中翻译调控的贡献。
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Integrative multi-omics analysis reveals the translational landscape of the plant-parasitic nematode Meloidogyne incognita.

Root-knot nematodes (RKNs) of the genus Meloidogyne pose the most significant threats to global food security due to their destructive nature as plant-parasitic nematodes. Although significant attention has been devoted to investigating the gene transcription profiling of RKNs, our understanding of the translational landscape of RKNs remains limited. In this study, we elucidated the translational landscape of Meloidogyne incognita through the integration of translatome, transcriptome and quantitative proteome analyses. Our findings revealed numerous previously unannotated translation events and refined the genome annotation. By investigating the genome-wide translational dynamics of M. incognita during parasitism, we revealed that the genes of M. incognita undergo parasitic stage-specific regulation at the translational level. Interestingly, we identified 470 micropeptides (containing fewer than 100 amino acids) with the potential to function as effectors. Additionally, we observed that the effector-coding genes in M. incognita exhibit higher translation efficiency (TE). Further analysis suggests that M. incognita has the potential to regulate the TE of effector-coding genes without simultaneous alterations in their transcript abundance, facilitating effector synthesis. Collectively, our study provides comprehensive datasets and explores the genome-wide translational landscape of M. incognita, shedding light on the contributions of translational regulation during parasitism.

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来源期刊
Communications Biology
Communications Biology Medicine-Medicine (miscellaneous)
CiteScore
8.60
自引率
1.70%
发文量
1233
审稿时长
13 weeks
期刊介绍: Communications Biology is an open access journal from Nature Research publishing high-quality research, reviews and commentary in all areas of the biological sciences. Research papers published by the journal represent significant advances bringing new biological insight to a specialized area of research.
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