Abstract

Here, we compared miRNA expression profiles in embryonic cell cultures of the conifer Picea balfouriana following application of the synthetic cytokinin 6-benzylaminopurine (6-BAP). We used next-generation sequencing to analyze three libraries of small RNAs from the treated embryogenic cell cultures and generated 24,000,000 raw reads from each of the libraries. Over 70 differentially regulated micro RNA (miRNA) families (≥2 fold change in expression) were identified between pairs of treatments. A quantitative analysis showed that miR3633 and miR1026 were upregulated in tissues with the highest embryogenic ability. These two miRNAs were predicted to target genes encoding receptor-like protein kinase and GAMYB transcription factors, respectively. In one library, miR1160, miR5638, miR1315, and miR5225 were downregulated. These four miRNAs were predicted to target genes encoding APETALA2, calmodulin-binding protein, and calcium-dependent protein kinase transcription factors. The expression patterns of the miRNAs and their targets were negatively correlated. Approximately 181 potentially novel P. balfouriana miRNAs were predicted from the three libraries, and seven were validated during the quantitative analysis. This study is the first report of differential miRNA regulation in tissues treated with 6-BAP during somatic embryogenesis. The differentially expressed miRNAs will be of value for investigating the mechanisms of embryogenic processes that are responsive to 6-BAP in P. balfouriana.

Highlights

  • Somatic embryogenesis (SE) is an important method in spruce breeding programs and enables the regeneration and cloning of trees with desirable genotypes

  • SRNA libraries were constructed by high-throughput sequencing of P. balfouriana callus cultures treated with three 6-BAP concentrations

  • After processing the sequencing data, we identified more than 4,000 conserved and 50 novel micro RNA (miRNA) in each library

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Summary

Introduction

Somatic embryogenesis (SE) is an important method in spruce breeding programs and enables the regeneration and cloning of trees with desirable genotypes. The callus tissue formed from some genotypes can gradually lose embryogenic capacity. The mechanism of this effect is unclear, as the early stages of SE are insufficiently known [1,2,3]. This mechanism has been investigated by identifying differentially expressed genes between embryogenic and nonembryogenic tissues in order to elucidate the molecular regulatory networks that operate during SE in plant species [4], including Picea abies (L.) H. The genetic regulation of these differentially expressed genes and their specific functions remain largely unknown

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