Liyong Sun, Yao Chen, Tangjie Nie, Xiaoxia Wan, Xuan Zou, Zheng Jiang, Huilin Zhu, Qiang Wei, Yaling Wang, Shuxian Li, Zengfang Yin
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The temporal dynamics of a large number of differentially expressed genes (DEGs) involved in multiple signaling (transduction) pathways contributed to multi-tepal primordia initiation during early floral differentiation. In particular, the dynamic expression of , , , and might be responsible for floral meristem activation and maintenance, while and potentially regulated floral organ initiation. Floral homeotic genes, such as , contributed to subsequent organ identity specialization. We further isolated a nucleus-localized APETALA3 homolog from , terming it the () gene, which was expressed in almost all vegetative and reproductive tissues. Ectopically expressing in resulted in altered phenotypes of rosette leaves, inflorescences, and florets, particularly generating extra petals instead of undergoing homeotic organ conversion. This discovery revealed an additional function of in regulating organ initiation in addition to its conserved B-function in floral architecture plasticity. In summary, the multi-tepals of originated from the early tepal primordia initiation event rather than stamen petalody. The formation of the multi-tepal trait was attributed to the coordinated regulation of several vital DEGs, with the gene playing an important role. These results provide additional insight into the regulation underlying the floral architecture formation in ancient species and suggest that manipulating the gene may hold promising potential for genetic breeding in ornamental plants.","PeriodicalId":13178,"journal":{"name":"Horticultural Plant Journal","volume":"237 1","pages":""},"PeriodicalIF":5.7000,"publicationDate":"2024-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"B-class floral homeotic gene MapoAPETALA3 may play an important role in the origin and formation of multi-tepals in Magnolia polytepala\",\"authors\":\"Liyong Sun, Yao Chen, Tangjie Nie, Xiaoxia Wan, Xuan Zou, Zheng Jiang, Huilin Zhu, Qiang Wei, Yaling Wang, Shuxian Li, Zengfang Yin\",\"doi\":\"10.1016/j.hpj.2023.08.004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In angiosperms, floral architecture diversity reflects its significance in exploring plant evolution. , an endemic and ancient species in China, possesses a unique multi-tepal trait. 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We further isolated a nucleus-localized APETALA3 homolog from , terming it the () gene, which was expressed in almost all vegetative and reproductive tissues. Ectopically expressing in resulted in altered phenotypes of rosette leaves, inflorescences, and florets, particularly generating extra petals instead of undergoing homeotic organ conversion. This discovery revealed an additional function of in regulating organ initiation in addition to its conserved B-function in floral architecture plasticity. In summary, the multi-tepals of originated from the early tepal primordia initiation event rather than stamen petalody. The formation of the multi-tepal trait was attributed to the coordinated regulation of several vital DEGs, with the gene playing an important role. 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引用次数: 0
摘要
在被子植物中,花结构的多样性反映了其在探索植物进化中的重要意义。中国特有的一个古老物种--榆叶梅,具有独特的多花被特征。值得注意的是,人们对这些多花被片的起源和形成知之甚少。在这项研究中,我们通过表型分析、测序和分子实验,研究了多花被片的起源和形成,并阐明了其背后的分子调控机制。我们发现,多花被片的形态解剖特征与正常花被片相似,但与瓣状雄蕊和正常雄蕊不同。在早期花分化过程中,涉及多种信号(传导)途径的大量差异表达基因(DEGs)的时间动态促进了多花被片原基的形成。其中,、、和的动态表达可能对花分生组织的激活和维持负责,而和则可能调控花器官的萌发。花的同源基因,如 、 和 ,有助于随后的器官特征特化。我们进一步从Ⅳ中分离出一个细胞核定位的APETALA3同源基因,称其为()基因,该基因在几乎所有无性和生殖组织中都有表达。异位表达in基因会导致莲座叶、花序和小花的表型发生改变,尤其是产生额外的花瓣,而不是进行同源器官转换。这一发现揭示了 in 除了在花卉结构可塑性中保守的 B 功能外,还具有调控器官萌发的其他功能。总之,多花被片起源于早期的花被片原基萌发,而不是雄蕊花瓣。多花被性状的形成归因于几个重要的 DEGs 的协调调控,其中该基因发挥了重要作用。这些结果进一步揭示了古老物种花卉结构形成的内在调控机制,并表明操纵该基因有可能为观赏植物的遗传育种带来希望。
B-class floral homeotic gene MapoAPETALA3 may play an important role in the origin and formation of multi-tepals in Magnolia polytepala
In angiosperms, floral architecture diversity reflects its significance in exploring plant evolution. , an endemic and ancient species in China, possesses a unique multi-tepal trait. Notably, the origin and formation of these multi-tepals are poorly understood. In this study, we investigated the origin and formation of multi-tepals from the inner floral whorl and elucidated the underlying molecular regulatory mechanisms by combining phenotypic analysis, sequencing, and molecular experiments. We found that the multi-tepals exhibited morpho-anatomical characteristics similar to normal tepals but differed from petaloid and normal stamens. The temporal dynamics of a large number of differentially expressed genes (DEGs) involved in multiple signaling (transduction) pathways contributed to multi-tepal primordia initiation during early floral differentiation. In particular, the dynamic expression of , , , and might be responsible for floral meristem activation and maintenance, while and potentially regulated floral organ initiation. Floral homeotic genes, such as , contributed to subsequent organ identity specialization. We further isolated a nucleus-localized APETALA3 homolog from , terming it the () gene, which was expressed in almost all vegetative and reproductive tissues. Ectopically expressing in resulted in altered phenotypes of rosette leaves, inflorescences, and florets, particularly generating extra petals instead of undergoing homeotic organ conversion. This discovery revealed an additional function of in regulating organ initiation in addition to its conserved B-function in floral architecture plasticity. In summary, the multi-tepals of originated from the early tepal primordia initiation event rather than stamen petalody. The formation of the multi-tepal trait was attributed to the coordinated regulation of several vital DEGs, with the gene playing an important role. These results provide additional insight into the regulation underlying the floral architecture formation in ancient species and suggest that manipulating the gene may hold promising potential for genetic breeding in ornamental plants.
期刊介绍:
Horticultural Plant Journal (HPJ) is an OPEN ACCESS international journal. HPJ publishes research related to all horticultural plants, including fruits, vegetables, ornamental plants, tea plants, and medicinal plants, etc. The journal covers all aspects of horticultural crop sciences, including germplasm resources, genetics and breeding, tillage and cultivation, physiology and biochemistry, ecology, genomics, biotechnology, plant protection, postharvest processing, etc. Article types include Original research papers, Reviews, and Short communications.