Transcriptional Dynamics Underlying Somatic Embryogenesis in Coffea canephora

In <i>Coffea canephora</i>, a direct somatic embryogenesis (SE) protocol has been established by pretreating plants with NAA and kinetin, followed by the induction of leaf explants in a liquid medium with BA. Through a transcriptomic analysis of 10 key moments of the induction of SE in <i>C. canephora</i>, we were able to establish that the transcriptional responses of this process are divided into four stages. These stages correspond to the pretreatment, characterized by the positive regulation of genes associated with cell wall remodeling, flavonoid biosynthesis, and antioxidant activity that prepare the explants for the intense cellular activity that represents the induction of SE. During the first few hours, the early response to induction occurs, characterized by the highest number of differentially expressed genes, most related to the response to multiple stimuli. At 24 h, a late response begins with the upregulation of genes related to energy production and the biosynthesis of amino acids. Finally, <i>WOX</i>, <i>BBM</i>, and <i>ABI3</i> genes are upregulated during the embryogenic response. The downregulation of genes related to the circadian cycle, photomorphogenesis, photosynthesis, and chloroplast components were observed throughout the process. The detailed analysis of the primary transcriptional responses that occur during the SE of <i>C. canephora</i> helps us to clarify how auxins and cytokinins orchestrate the integration of different networks of plant metabolism and lead to the development of somatic embryos.

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Publication Details

Journal
Plants
Published
2025-04-02
DOI
https://doi.org/10.3390/plants14071108
Citations
2
Primary Topic
Plant tissue culture and regeneration
Type
article
Field-Weighted Citation Impact
1.61
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article

Transcriptional Dynamics Underlying Somatic Embryogenesis in Coffea canephora

Rosa M. Galáz-Ávalos, Hugo A. Méndez-Hernández, Enrique Ibarra‐Laclette, Ana O. Quintana-Escobar et al.
2 citations
Plants
Plant tissue culture and regeneration
1.61
article

Transcriptional Dynamics Underlying Somatic Embryogenesis in Coffea canephora

Rosa M. Galáz-Ávalos, Hugo A. Méndez-Hernández, Enrique Ibarra‐Laclette, Ana O. Quintana-Escobar, Víctor M. Loyola‐Vargas, Marcos-David Couoh-Cauich
article en
2 citations

Abstract

In <i>Coffea canephora</i>, a direct somatic embryogenesis (SE) protocol has been established by pretreating plants with NAA and kinetin, followed by the induction of leaf explants in a liquid medium with BA. Through a transcriptomic analysis of 10 key moments of the induction of SE in <i>C. canephora</i>, we were able to establish that the transcriptional responses of this process are divided into four stages. These stages correspond to the pretreatment, characterized by the positive regulation of genes associated with cell wall remodeling, flavonoid biosynthesis, and antioxidant activity that prepare the explants for the intense cellular activity that represents the induction of SE. During the first few hours, the early response to induction occurs, characterized by the highest number of differentially expressed genes, most related to the response to multiple stimuli. At 24 h, a late response begins with the upregulation of genes related to energy production and the biosynthesis of amino acids. Finally, <i>WOX</i>, <i>BBM</i>, and <i>ABI3</i> genes are upregulated during the embryogenic response. The downregulation of genes related to the circadian cycle, photomorphogenesis, photosynthesis, and chloroplast components were observed throughout the process. The detailed analysis of the primary transcriptional responses that occur during the SE of <i>C. canephora</i> helps us to clarify how auxins and cytokinins orchestrate the integration of different networks of plant metabolism and lead to the development of somatic embryos.

PlantsVol. 14(7)
Secretaría de Investigación, Innovación y Educación Superior (MX), Instituto de Ecología (MX)
Affordable and clean energy
Openalex Percentile: Top 18%
Plant tissue culture and regeneration
1.61
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