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Article|28 Feb 2024|OPEN
Transcriptomic analyses to summarize gene expression patterns that occur during leaf initiation of Chinese cabbage
XiaoXue Sun1,3 , Zihan Liu2,3 , Rui Liu1 , Johan Bucher2 and Jianjun Zhao1 , , Richard G.F. Visser2 , , Guusje Bonnema,2 ,
1State Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Ministry of Education of China-Hebei Province Joint Innovation Center for Efficient Green Vegetable Industry, College of Horticulture, Hebei Agricultural University, Baoding 071000, China
2Plant Breeding, Wageningen University & Research, 6708 PB Wageningen, The Netherlands
3Co-first authors
*Corresponding author. E-mail: jjz1971@aliyun.com,richard.visser@wur.nl,guusje.bonnema@wur.nl

Horticulture Research 11,
Article number: uhae059 (2024)
doi: https://doi.org/10.1093/hr/uhae059
Views: 1407

Received: 25 Aug 2023
Accepted: 19 Feb 2024
Published online: 28 Feb 2024

Abstract

In Chinese cabbage, rosette leaves expose their adaxial side to the light converting light energy into chemical energy, acting as a source for the growth of the leafy head. In the leafy head, the outer heading leaves expose their abaxial side to the light while the inner leaves are shielded from the light and have become a sink organ of the growing Chinese cabbage plant. Interestingly, variation in several ad/abaxial polarity genes is associated with the typical leafy head morphotype. The initiation of leaf primordia and the establishment of leaf ad/abaxial polarity are essential steps in the initiation of marginal meristem activity leading to leaf formation. Understanding the molecular genetic mechanisms of leaf primordia formation, polar differentiation, and leaf expansion is thus relevant to understand leafy head formation. As Brassica's are mesa-hexaploids, many genes have multiple paralogues, complicating analysis of the genetic regulation of leaf development. In this study, we used laser dissection of Chinese cabbage leaf primordia and the shoot apical meristem (SAM) to compare gene expression profiles between both adaxial and abaxial sides and the SAM aiming to capture transcriptome changes underlying leaf primordia development. We highlight genes with roles in hormone pathways and transcription factors. We also assessed gene expression gradients along expanded leaf blades from the same plants to analyze regulatory links between SAM, leaf primordia and the expanding rosette leaf. The catalogue of differentially expressed genes provides insights in gene expression patterns involved in leaf development and form a starting point to unravel leafy head formation.