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Endogenous Nod-factor-like signal molecules promote early somatic embryo development in Norway spruce. | LitMetric

AI Article Synopsis

  • Embryogenic cultures of Norway spruce are made up of pro-embryogenic masses (PEMs) and somatic embryos, with auxin being crucial for PEM development; its removal leads to cell death.
  • Extracts from embryogenic cultures can promote PEM growth in auxin-deficient environments, and researchers have identified the active compound as a lipophilic chitin oligosaccharide (LCO).
  • The presence of LCO is linked to PEM development stages, and adding LCO or similar compounds can prevent cell death caused by auxin depletion, suggesting LCO plays a vital signaling role in embryo development.

Article Abstract

Embryogenic cultures of Norway spruce (Picea abies) are composed of pro-embryogenic masses (PEMs) and somatic embryos of various developmental stages. Auxin is important for PEM formation and proliferation. In this report we show that depletion of auxin blocks PEM development and causes large-scale cell death. Extracts of the media conditioned by embryogenic cultures stimulate development of PEM aggregates in auxin-deficient cultures. Partial characterization of the conditioning factor shows that it is a lipophilic, low-molecular-weight molecule, which is sensitive to chitinase and contains GlcNAc residues. On the basis of this information, we propose that the factor is a lipophilic chitin oligosaccharide (LCO). The amount of LCO correlates to the developmental stages of PEMs and embryos, with the highest level in the media conditioned by developmentally blocked cultures. LCO is not present in nonembryogenic cultures. Cell death, induced by withdrawal of auxin, is suppressed by extra supply of endogenous LCO or Nod factor from Rhizobium sp. NGR234. The effect can be mimicked by a chitotetraose or chitinase from Streptomyces griseus. Taken together, our data suggest that endogenous LCO acts as a signal molecule stimulating PEM and early embryo development in Norway spruce.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC148915PMC
http://dx.doi.org/10.1104/pp.010547DOI Listing

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