Abstract

Somatic embryogenesis (SE) is a process of somatic cells that dedifferentiate to totipotent embryonic stem cells and generate embryos in vitro. Despite recent scientific headway in deciphering the difficulties of somatic embryogenesis, the overall picture of key genes, pathways, and co-expression networks regulating SE is still fragmented. Therefore, deciphering the molecular basis of somatic embryogenesis of hybrid sweetgum remains pertinent. In the present study, we analyzed the transcriptome profiles and gene expression regulation changes via RNA sequencing from three distinct developmental stages of hybrid sweetgum: non-embryogenic callus (NEC), embryogenic callus (EC), and redifferentiation. Comparative transcriptome analysis showed that 19,957 genes were differentially expressed in ten pairwise comparisons of SE. Among these, plant hormone signaling-related genes, especially the auxin and cytokinin signaling components, were significantly enriched in NEC and EC early. The K-means method was used to identify multiple transcription factors, including HB-WOX, B3-ARF, AP2/ERF, and GRFs (growth regulating factors). These transcription factors showed distinct stage- or tissue-specific expression patterns mirroring each of the 12 superclusters to which they belonged. For example, the WOX transcription factor family was expressed only at NEC and EC stages, ARF transcription factor was expressed in EC early, and GRFs was expressed in late SE. It was noteworthy that the AP2/ERF transcription factor family was expressed during the whole SE process, but almost not in roots, stems and leaves. A weighted gene co-expression network analysis (WGCNA) was used in conjunction with the gene expression profiles to recognize the genes and modules that may associate with specific tissues and stages. We constructed co-expression networks and revealed 22 gene modules. Four of these modules with properties relating to embryonic potential, early somatic embryogenesis, and somatic embryo development, as well as some hub genes, were identified for further functional studied. Through a combination analysis of WGCNA and K-means, SE-related genes including AUX22, ABI3, ARF3, ARF5, AIL1, AIL5, AGL15, WOX11, WOX9, IAA29, BBM1, MYB36, LEA6, SMR4 and others were obtained, indicating that these genes play an important role in the processes underlying the progression from EC to somatic embryos (SEs) morphogenesis. The transcriptome information provided here will form the foundation for future research on genetic transformation and epigenetic control of plant embryogenesis at a molecular level. In follow-up studies, these data could be used to construct a regulatory network for SE; Key genes obtained from coexpression network analysis at each critical stage of somatic embryo can be considered as potential candidate genes to verify these networks.

Highlights

  • Chinese sweetgum (Liquidambar formosana Hance) is distributed in most temperate and subtropical regions of China and is used mainly for medicinal and ornamental purposes (Sun et al, 2016)

  • There are 4 candidate genes that seem to affect the maintain of totipotency, like the homeotic transcription factor WOX9, an important regulator of plant stem cell fate in the shoot meristem, which may regulate the stem cell fate in the callus; the BBM1 transcription factor involved in the growth regulation of organ primordia; the R2R3MYB transcription factors are involved in cell proliferation and elongation, which may promote callus proliferation

  • MYB15 was involved in drought and salt tolerance and may enhance expression levels of genes involved in abscisic acid (ABA) biosynthesis and signaling, as well as those encoding stressprotective proteins

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Summary

Introduction

Chinese sweetgum (Liquidambar formosana Hance) is distributed in most temperate and subtropical regions of China and is used mainly for medicinal and ornamental purposes (Sun et al, 2016). American sweetgum (Liquidambar styraciflua L.) is a common southern American hardwood that has become an important feedstock for the timber and paper industries. These two species are interfertile even after 10 million years of separation (Vendrame et al, 2001). The breeding of hybrid sweetgum is expected to have great potential value for the wood industry. We successfully developed a SE system for hybrid sweetgum from hybrid immature seed explants. This system will be the foundation for breeding research and large-scale propagation of hybrid sweetgum. The mechanism of its SE remains unclear, which strongly hampers the advancement of breeding research and efficient propagation

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