Genotype and transcriptome effects on somatic embryogenesis in Cryptomeria japonica

PLoS One. 2020 Dec 29;15(12):e0244634. doi: 10.1371/journal.pone.0244634. eCollection 2020.

Abstract

Somatic embryogenesis (SE), which is in vitro regeneration of plant bodies from somatic cells, represents a useful means of clonal propagation and genetic engineering of forest trees. While protocols to obtain calluses and induce regeneration in somatic embryos have been reported for many tree species, the knowledge of molecular mechanisms of SE development is still insufficient to achieve an efficient supply of somatic embryos required for the industrial application. Cryptomeria japonica, a conifer species widely used for plantation forestry in Japan, is one of the tree species waiting for a secure SE protocol; the probability of normal embryo development appears to depend on genotype. To discriminate the embryogenic potential of embryonal masses (EMs) and efficiently obtain normal somatic embryos of C. japonica, we investigated the effects of genotype and transcriptome on the variation in embryogenic potential. Using an induction experiment with 12 EMs each from six genotypes, we showed that embryogenic potential differs between/within genotypes. Comparisons of gene expression profiles among EMs with different embryogenic potentials revealed that 742 differently expressed genes were mainly associated with pattern forming and metabolism. Thus, we suggest that not only genotype but also gene expression profiles can determine success in SE development. Consistent with previous findings for other conifer species, genes encoding leafy cotyledon, wuschel, germin-like proteins, and glutathione-S-transferases are likely to be involved in SE development in C. japonica and indeed highly expressed in EMs with high-embryogenic potential; therefore, these proteins represent candidate markers for distinguishing embryogenic potential.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cryptomeria / genetics
  • Cryptomeria / growth & development*
  • Gene Expression Profiling / methods*
  • Gene Expression Regulation, Developmental
  • Gene Expression Regulation, Plant
  • Gene Regulatory Networks*
  • Genetic Variation
  • Genotype
  • Japan
  • Plant Proteins
  • Plant Somatic Embryogenesis Techniques / methods*
  • Sequence Analysis, RNA

Substances

  • Plant Proteins

Grants and funding

This work was supported in part by grants from the Ministry of Agriculture, Forestry and Fisheries of Japan and NARO Bio-oriented Technology Research Advancement Institution to Y. M. (No. 28013B and No. 28013BC). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.