超越亲本系:多组学分析揭示了水稻×水稻杂种优势的表观遗传和转录机制

IF 5.7 1区 生物学 Q1 PLANT SCIENCES
Xin Peng, Yahui Wu, Yuli Gan, Jiantao Tan, Qian Qian, MengYuan Shen, Kangli Sun, Xing Huo, Degui Zhou, Qi Liu
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引用次数: 0

摘要

杂种优势,或称杂种优势,是指杂种比其亲本具有优越的表型,在农业上得到了广泛的应用。稻属种间杂交种在水稻品种的系统改良中显示出巨大的潜力。然而,水稻种间杂交种杂种优势的机制基础仍然知之甚少。在这里,我们系统地使用Oryza sativa L. ssp进行表型表征,全基因组亚硫酸盐测序,RNA测序和小RNA分析。粳稻的履历。Nipponbare (NIP), Oryza rufipogon Griff。acc。CWR,以及它们产生的F1杂交(命名为NC)。NIP和CWR表现出明显的表型和分子差异。种间杂交种NC表现出显著的产量优势。在杂交种中,大多数表观遗传和转录特征表现出相对于亲本系的加性遗传模式。分析显示,驯化选择基因在杂交和亲本中保持相对较低的DNA甲基化,并具有较高的表达水平。此外,我们发现非加性mirna可能参与调节杂种的生育、细胞生长和细胞分裂过程。DNA甲基化水平与基因表达呈显著负相关。功能富集分析表明,杂交mpv基因与开花时间调控、碳水化合物代谢、光合作用、蛋白质磷酸化、种子发育和防御反应显著相关。通过加权基因共表达网络分析,鉴定出102个功能基因模块,其中6个与产量相关杂种优势显著相关。总的来说,我们的研究结果提供了一个多组学框架来理解精英品种和野生水稻近缘种间杂交,突出了CWR作为水稻改良的一个未开发的遗传库。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Beyond parental lines: multi-omics analyses reveal epigenetic and transcriptional mechanisms underlying heterosis in Oryza sativa × Oryza rufipogon hybrids

Heterosis, or hybrid vigor, refers to the superior phenotypes of a hybrid compared with their parents and is widely exploited in agriculture. Interspecific hybrids within the Oryza genus demonstrate significant potential for the systematic improvement of rice varieties. Nevertheless, the mechanistic basis underlying heterosis in interspecific Oryza hybrids remains poorly understood. Here, we systematically performed phenotypic characterization, whole-genome bisulfite sequencing, RNA sequencing, and small RNA profiling using Oryza sativa L. ssp. japonica cv. Nipponbare (NIP), Oryza rufipogon Griff. acc. CWR, and their resulting F1 hybrid (named as NC). NIP and CWR showed distinct phenotypic and molecular differences. The interspecific hybrid, NC, exhibited significant yield heterosis. In the hybrid, most epigenetic and transcriptional features displayed additive inheritance patterns relative to parental lines. Analysis revealed that domestication-selected genes maintained relatively low DNA methylation coupled with high expression levels in both hybrid and parental lines. Additionally, we identified that non-additive miRNAs were potentially involved in regulating fertility, cell growth, and cell division processes in the hybrid. A significant negative correlation was observed between DNA methylation level and gene expression. Functional enrichment analysis revealed that hybrid-MPV DEGs were significantly associated with flowering time regulation, carbohydrate metabolism, photosynthesis, protein phosphorylation, seed development, and defense responses. Through weighted gene co-expression network analysis, we identified 102 functional gene modules, six of which were significantly associated with yield-related heterosis. Collectively, our results provide a multi-omics framework for understanding interspecific hybridization between elite cultivars and wild rice relatives, highlighting CWR as an untapped genetic reservoir for rice improvement.

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来源期刊
The Plant Journal
The Plant Journal 生物-植物科学
CiteScore
13.10
自引率
4.20%
发文量
415
审稿时长
2.3 months
期刊介绍: Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community. Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.
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