文献类型：期刊文献

英文题名：Floral organ transcriptome in Camellia sasanqua provided insight into stamen petaloid

作者：Fan, Menglong[1,2] Li, Xinlei[1] Zhang, Ying[1] Wu, Si[1] Song, Zhixin[1] Yin, Hengfu[1] Liu, Weixin[1] Fan, Zhengqi[1] Li, Jiyuan[1]

第一作者：Fan, Menglong

通信作者：Li, XL[1]

机构：[1]Chinese Acad Forestry, Res Inst Subtrop Forestry, Hangzhou 311400, Zhejiang, Peoples R China;[2]Chinese Acad Forestry, Res Inst Forestry, Beijing 100091, Peoples R China

年份：2022

卷号：22

期号：1

外文期刊名：BMC PLANT BIOLOGY

收录：;WOS:【SCI-EXPANDED(收录号:WOS:000864299500001)】；

基金：This work was supported by National Key R&D Program of China [2020YFD1000500] and Zhejiang Basic and Public Welfare Research Program [LGN20C160006].

语种：英文

外文关键词：Camellia sasanqua; Double flower; Transcriptome; Petaloid stamen; ABCE model; Phytohormone

摘要：Background The cultivated Camellia sasanqua forms a divergent double flower pattern, and the stamen petaloid is a vital factor in the phenomenon. However, the regulation mechanism remains largely unclear. Results Here, a comprehensive comparative transcriptome analysis of the wild-type, "semi-double", "peony double", and "rose double" was performed. The cluster analysis of global gene expression level showed petal and stamen difficulty separable in double flower. The crucial pathway and genes related to double flower patterns regulation were identified by pairwise comparisons and weighted gene coexpression network (WGCNA). Divergent genes expression, such as AUX1 and AHP, are involved in plant hormone signaling and photosynthesis, and secondary metabolites play an important role. Notably, the diversity of a petal-specific model exhibits a similar molecular signature to the stamen, containing extensin protein and PSBO1, supporting the stamen petaloid point. Moreover, the expansion of class A gene activity influenced the double flower formation, showing that the key function of gene expression was probably demolished. Conclusions Overall, this work confirmed the ABCE model and provided new insights for elucidating the molecular signature of double formation.