Transcriptome analysis provides insights into xylogenesis formation in Moso bamboo (Phyllostachys edulis) shoot

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作者
Hui Zhang
Ye-qing Ying
Jie Wang
Xian-hai Zhao
Wei Zeng
Cherie Beahan
Jun-bo He
Xiao-yang Chen
Antony Bacic
Li-li Song
Ai-min Wu
机构
[1] Zhejiang A&F University,State Key Laboratory of Subtropical Silviculture, School of Forestry and Biotechnology
[2] Lin’an,College of Forest
[3] Guangdong Key Laboratory for Innovative Development and Utilization of Forest Plant Germplasm,ARC Center of Excellence in Plant Cell Walls, School of BioSciences
[4] South China Agricultural University,undefined
[5] the University of Melbourne,undefined
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Maturation-related changes in cell wall composition and the molecular mechanisms underlying cell wall changes were investigated from the apical, middle and basal segments in moso bamboo shoot (MBS). With maturation extent from apical to basal regions in MBS, lignin and cellulose content increased, whereas heteroxylan exhibited a decreasing trend. Activities of phenylalanine amonnialyase (PAL), cinnamyl alcohol dehydrogenase (CAD) and cinnamate-4-hydroxylase (C4H), which are involved in lignin biosynthesis, increased rapidly from the apex to the base sections. The comparative transcriptomic analysis was carried out to identify some key genes involved in secondary cell walls (SCW) formation underlying the cell wall compositions changes including 63, 8, 18, and 31 functional unigenes encoding biosynthesis of lignin, cellulose, xylan and NAC-MYB-based transcription factors, respectively. Genes related to secondary cell wall formation and lignin biosynthesis had higher expression levels in the middle and basal segments compared to those in the apical segments. Furthermore, the expression profile of PePAL gene showed positive relationships with cellulose-related gene PeCESA4, xylan-related genes PeIRX9 and PeIRX10. Our results indicated that lignification occurred in the more mature middle and basal segments in MBS at harvest while lignification of MBS were correlated with higher expression levels of PeCESA4, PeIRX9 and PeIRX10 genes.
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