{"title":"翻译景观为亚种间杂交水稻杂种优势的分子机制提供了新的视角","authors":"Zengde Xi, Mengyao Wang, Fei Wang, Jianbo Wang","doi":"10.1111/tpj.70297","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Heterosis has been widely applied in crop breeding and has significantly improved grain yield worldwide. Many studies have attempted to elucidate heterosis from various perspectives; however, its genetic basis—especially at the translational level—remains elusive. In this study, we performed RNA-seq and ribosome profiling on the inter-subspecific hybrid rice ZY19 (<i>Oryza sativa</i> L. subsp. <i>indica</i> Kato × <i>O. sativa</i> L. subsp. <i>japonica</i> Kato) and its parental lines to examine genome-wide translational dynamics. Differential gene expression between the hybrid and its parents revealed a strong discordance between transcriptional and translational levels, and translational regulation appeared to buffer the transcriptional differences. Although additive and non-additive gene expression patterns shifted during translation, additive expression remained the predominant pattern at the translational level in the hybrid. Moreover, a high proportion of single-parent expression genes also exhibited additive expression. In the hybrid, allele-specific expression (ASE) was differentially regulated in transcription and translation. Notably, <i>cis</i> and <i>trans</i>-regulation tended to function independently in transcription, whereas they were more likely to act together in translation. Finally, we investigated the effects of various regulatory mechanisms and elements on translation and found that genes with more alternative splicing (AS) events had a lower translational efficiency (TE) than genes with fewer AS events. In addition, translation was repressed by the upstream open reading frames (uORFs), downstream open reading frames (dORFs), N<sup>6</sup>-methyladenosines (m<sup>6</sup>As) and microRNAs (miRNAs). Overall, our study provides new insights into the molecular mechanisms of heterosis in inter-subspecific hybrid rice.</p>\n </div>","PeriodicalId":233,"journal":{"name":"The Plant Journal","volume":"122 6","pages":""},"PeriodicalIF":6.2000,"publicationDate":"2025-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Translational landscape provides insight into the molecular mechanism of heterosis in inter-subspecific hybrid rice\",\"authors\":\"Zengde Xi, Mengyao Wang, Fei Wang, Jianbo Wang\",\"doi\":\"10.1111/tpj.70297\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>Heterosis has been widely applied in crop breeding and has significantly improved grain yield worldwide. Many studies have attempted to elucidate heterosis from various perspectives; however, its genetic basis—especially at the translational level—remains elusive. 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Notably, <i>cis</i> and <i>trans</i>-regulation tended to function independently in transcription, whereas they were more likely to act together in translation. Finally, we investigated the effects of various regulatory mechanisms and elements on translation and found that genes with more alternative splicing (AS) events had a lower translational efficiency (TE) than genes with fewer AS events. In addition, translation was repressed by the upstream open reading frames (uORFs), downstream open reading frames (dORFs), N<sup>6</sup>-methyladenosines (m<sup>6</sup>As) and microRNAs (miRNAs). 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引用次数: 0
摘要
杂种优势在作物育种中得到了广泛的应用,并在世界范围内显著提高了粮食产量。许多研究试图从不同的角度阐明杂种优势;然而,它的遗传基础——尤其是在翻译水平上——仍然难以捉摸。在本研究中,我们对杂交水稻ZY19 (Oryza sativa L. subsp.)进行了RNA-seq和核糖体分析。籼稻(Kato × O. sativa L.)日本加藤(japonica Kato)及其亲本系研究全基因组翻译动力学。杂种与亲本之间的差异基因表达揭示了转录和翻译水平之间的强烈不一致,翻译调控似乎可以缓冲转录差异。虽然加性和非加性基因表达模式在翻译过程中发生了变化,但在翻译水平上,加性表达仍然是杂种的主要表达模式。此外,高比例的单亲表达基因也表现出加性表达。在杂交中,等位基因特异性表达(ASE)在转录和翻译中受到差异调控。值得注意的是,顺式和反式调控往往在转录中独立起作用,而在翻译中它们更有可能一起起作用。最后,我们研究了各种调控机制和元件对翻译的影响,发现选择性剪接(AS)事件较多的基因的翻译效率(TE)低于选择性剪接(AS)事件较少的基因。此外,翻译还受到上游开放阅读框(uorf)、下游开放阅读框(dorf)、n6 -甲基腺苷(m6As)和microrna (miRNAs)的抑制。本研究为亚种间杂交稻杂种优势的分子机制提供了新的认识。
Translational landscape provides insight into the molecular mechanism of heterosis in inter-subspecific hybrid rice
Heterosis has been widely applied in crop breeding and has significantly improved grain yield worldwide. Many studies have attempted to elucidate heterosis from various perspectives; however, its genetic basis—especially at the translational level—remains elusive. In this study, we performed RNA-seq and ribosome profiling on the inter-subspecific hybrid rice ZY19 (Oryza sativa L. subsp. indica Kato × O. sativa L. subsp. japonica Kato) and its parental lines to examine genome-wide translational dynamics. Differential gene expression between the hybrid and its parents revealed a strong discordance between transcriptional and translational levels, and translational regulation appeared to buffer the transcriptional differences. Although additive and non-additive gene expression patterns shifted during translation, additive expression remained the predominant pattern at the translational level in the hybrid. Moreover, a high proportion of single-parent expression genes also exhibited additive expression. In the hybrid, allele-specific expression (ASE) was differentially regulated in transcription and translation. Notably, cis and trans-regulation tended to function independently in transcription, whereas they were more likely to act together in translation. Finally, we investigated the effects of various regulatory mechanisms and elements on translation and found that genes with more alternative splicing (AS) events had a lower translational efficiency (TE) than genes with fewer AS events. In addition, translation was repressed by the upstream open reading frames (uORFs), downstream open reading frames (dORFs), N6-methyladenosines (m6As) and microRNAs (miRNAs). Overall, our study provides new insights into the molecular mechanisms of heterosis in inter-subspecific hybrid rice.
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.