Abstract

BackgroundWood formation affects the chemical and physical properties of wood, and thus affects its utility as a building material or a feedstock for biofuels, pulp and paper. To obtain genome-wide insights on the transcriptome changes and regulatory networks in wood formation, we used high-throughput RNA sequencing to characterize cDNA libraries of mature xylem from tension wood (TW), opposite wood (OW), and normal wood (NW), in the industrial tree species Populus tomentosa.ResultsOur sequencing generated 140,978,316 (TW), 128,972,228 (OW), and 117,672,362 (NW) reads, corresponding to 10,127 (TW), 10,129 (OW), and 10,129 (NW) unique genes. Of these, 361 genes were differentially transcribed between TW and OW (log2FC ≥ 1 or ≤ -1, FDR < 0.05), 2,658 differed between OW and NW, and 2,417 differed between TW and NW. This indicates that NW differs significantly from the wood in branches; GO term analysis also indicated that OW experienced more transcriptome remodeling. The differentially expressed genes included 97 encoding transcription factors (TFs), 40 involved in hormone signal transduction, 33 in lignin biosynthesis, 21 in flavonoid biosynthesis, and 43 in cell wall metabolism, including cellulose synthase, sucrose synthase, and COBRA. More than half of the differentially expressed TF showed more than 4-fold lower transcript levels in NW compared with TW or OW, indicating that TF abundances differed dramatically in different wood types and may have important roles in the formation of reaction wood. In addition, transcripts of most of the genes involved in lignin biosynthesis were more abundant in OW compared with TW, consistent with the higher lignin content of OW. We constructed two transcriptomic networks for the regulation of lignin and cellulose biosynthesis, including TFs, based on the co-expression patterns of different genes. Lastly, we used reverse transcription quantitative PCR to validate the differentially expressed genes identified.ConclusionsHere, we identified the global patterns and differences in gene expression among TW, OW, and NW, and constructed two transcriptomic regulatory networks involved in TW formation in P. tomentosa. We also identified candidate genes for molecular breeding of wood quality, and provided a starting point to decipher the molecular mechanisms of wood formation in Populus.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-1390-y) contains supplementary material, which is available to authorized users.

Highlights

  • Wood formation affects the chemical and physical properties of wood, and affects its utility as a building material or a feedstock for biofuels, pulp and paper

  • All genes showed similar patterns of expression in the three libraries (Figure 1). These analyses indicate that the RNA sequencing (RNA-seq) experiments conducted in this study were sufficiently reliable for the identification of genes that are differentially transcribed in the three wood tissues

  • Among the genes related to the cell wall, we found two differentially expressed genes encoding sucrose synthase (SUS), Pt-SUS1 (NW > opposite wood (OW) > tension wood (TW)) and Pt-SUS2 (OW > TW > normal wood (NW)), and their transcript levels indicated that different SUS genes have distinct expression patterns in NW and TW

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Summary

Introduction

Wood formation affects the chemical and physical properties of wood, and affects its utility as a building material or a feedstock for biofuels, pulp and paper. Many studies have used microarray analysis of TW and OW in artificially or naturally bent trunks of Populus to identify key genes that contribute to the formation of reaction wood, including genes encoding plant hormones, lignin and cellulose biosynthetic enzymes, and transcription factors (TFs) and other potential regulators [3,4,5,6]. 4-CoumarateCoA Ligase (4CL) expression increases during CW formation in pine species [7] and transgenic suppression of 4CL in Pinus radiata decreased lignin contents [8]. Plant hormones such as auxin, ethylene, and gibberellin have important roles in the formation of TW [2]. Recent work reported that the formation of TW and stem gravitropism in Acacia mangium seedlings requires gibberellins [10]

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