利用加权基因共表达网络分析(WGCNA)与定量性状基因座(QTL)图谱联合鉴定水稻耐厌氧发芽的关键基因和途径

IF 4.8 1区 农林科学 Q1 AGRONOMY
Rice Pub Date : 2024-05-31 DOI:10.1186/s12284-024-00714-y
Ming Yin, Zhenzhen Zheng, Yue Zhang, Shanwen Wang, Liying Zuo, Yuxin Lei, Yaqiong Zhao, Xiuqin Zhao, Binying Fu, Yingyao Shi, Jianlong Xu, Wensheng Wang
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引用次数: 0

摘要

背景:水稻是世界上最重要的粮食作物之一:水稻是世界上最重要的粮食作物之一,随着水稻直播方法的发展,无氧胁迫已成为限制水稻生长的一个主要因素:在本实验中,我们测试了水稻品种 NIP 和 HD84 对厌氧发芽的耐受性,并以它们为亲本构建了一个 DH(双倍单倍体)群体。对NIP(高耐性)和HD86(不耐性)及其后代HR(高耐性)和NHR(不耐性)在正常和厌氧环境下的转录组进行了测序。对差异表达基因(DEGs)进行了 GO(基因本体论)、KEGG(京都基因和基因组百科全书)和 WGCNA 分析。DH 群体的 QTL 图谱确定了对厌氧发芽相关染色体片段的耐受性。将 24 个样本的转录组结果与 159 个 DH 群体品系的厌氧胁迫 QTL 结果相结合,构建了一个代谢网络以确定关键通路,并构建了一个基因相互作用网络以研究关键基因。对关键基因首先进行了严格的功能验证,然后进行了全面分析,旨在阐明其在驯化和育种实践中的潜在用途,尤其侧重于对显性单倍型的利用:结果表明,丙酮酸脱羧酶(PDC)和乙醇脱氢酶(ADH)是茎秆长度生长的能量代谢起始信号,辅助素转运体 EXPA 是茎秆长度生长的决定信号。关键基因 Os05g0498700 和 Os01g0866100 对颖花长度具有负调控作用,最终提高了水稻对厌氧发芽的耐受性。育种潜力分析强调了 Os05g0498700-hyp2 和 Os01g0866100-hyp2 的附加价值,突出了它们在通过育种计划进一步改良水稻方面的潜在作用。我们的研究结果将为培育耐厌氧水稻品种提供理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Identification of Key Genes and Pathways for Anaerobic Germination Tolerance in Rice Using Weighted Gene Co-Expression Network Analysis (WGCNA) in Association with Quantitative Trait Locus (QTL) Mapping.

Identification of Key Genes and Pathways for Anaerobic Germination Tolerance in Rice Using Weighted Gene Co-Expression Network Analysis (WGCNA) in Association with Quantitative Trait Locus (QTL) Mapping.

Background: Rice is one of the most important food crops in the world, and with the development of direct seeding methods for rice, exposure to anaerobic stress has become a major factor limiting its growth.

Results: In this experiment, we tested the tolerance to anaerobic germination of rice varieties NIP and HD84, and they were used as parents to construct a DH (doubled-haploid) population. The transcriptomes of NIP (highly tolerant) and HD86 (intolerant), and their progeny HR (highly tolerant) and NHR (intolerant) were sequenced from normal and anaerobic environments. The differentially-expressed genes (DEGs) were subjected to GO (Gene ontology), KEGG (Kyoto Encyclopedia of Genes and Genomes), and WGCNA analyses. QTL mapping of the DH population identified tolerance to anaerobic germination-related chromosomal segments. The transcriptome results from 24 samples were combined with the anaerobic stress QTL results for 159 DH population lines to construct a metabolic network to identify key pathways and a gene interaction network to study the key genes. Essential genes were initially subjected to rigorous functional validation, followed by a comprehensive analysis aimed at elucidating their potential utility in domestication and breeding practices, particularly focusing on the exploitation of dominant haplotypes.

Conclusion: The results show that pyruvate decarboxylase (PDC) and alcohol dehydrogenase (ADH) are the starting signals of energy metabolism for coleoptile length growth, the auxin transporter EXPA is the determining signal for coleoptile length growth. The pivotal genes Os05g0498700 and Os01g0866100 exert a negative regulatory influence on coleoptile length, ultimately enhancing tolerance to anaerobic germination in rice. Analyses of breeding potential underscore the additional value of Os05g0498700-hyp2 and Os01g0866100-hyp2, highlighting their potential utility in further improving rice through breeding programs. The results of our study will provide a theoretical basis for breeding anaerobic-tolerant rice varieties.

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来源期刊
Rice
Rice AGRONOMY-
CiteScore
10.10
自引率
3.60%
发文量
60
审稿时长
>12 weeks
期刊介绍: Rice aims to fill a glaring void in basic and applied plant science journal publishing. This journal is the world''s only high-quality serial publication for reporting current advances in rice genetics, structural and functional genomics, comparative genomics, molecular biology and physiology, molecular breeding and comparative biology. Rice welcomes review articles and original papers in all of the aforementioned areas and serves as the primary source of newly published information for researchers and students in rice and related research.
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