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Updated: Aug 5, 2026

A Microfluidics Approach for the Functional Investigation of Signaling Oscillations Governing Somitogenesis
Published on: March 19, 2021
TOR Signaling as a Central Integrator of Embryogenic Reprogramming During 2,4-D-Induced Somatic Embryogenesis
José Luis Cabrera-Ponce1, Alex Ricardo Bermudez-Valle2, Maria Del Rosario Cárdenas-Aquino3
1Departamento de Ingeniería Genética, PlanTECC, Centro de Investigación y de Estudios Avanzados del IPN, Unidad Irapuato, Irapuato 36824, Guanajuato, Mexico.
Target Of Rapamycin (TOR) signaling integrates plant development, metabolism, and genome stability for somatic embryogenesis (SE). This study identifies TOR as a hub coordinating gene expression and metabolic pathways crucial for plant regeneration and genetic engineering.
Area of Science:
- Plant Biology
- Molecular Biology
- Biotechnology
Background:
- 2,4-Dichlorophenoxyacetic acid (2,4-D) is a widely used herbicide that induces somatic embryogenesis (SE) in plants.
- The precise molecular mechanisms linking hormonal signaling, metabolic changes, and translational control during SE induction remain unclear.
- Target Of Rapamycin (TOR) signaling is a key regulator of cell growth and metabolism, potentially playing an integrative role in SE.
Purpose of the Study:
- To investigate the systems-level regulatory mechanisms of 2,4-D-induced somatic embryogenesis.
- To determine if TOR signaling acts as an integrative hub coordinating key cellular processes during SE.
- To identify molecular targets for improving plant regeneration and genetic engineering applications.
Main Methods:
- Integration of publicly available transcriptomic data from Arabidopsis thaliana.
- High-confidence protein-protein interaction (PPI) network analysis using STRING v12.0.
- Identification and module analysis of upregulated genes and regulatory axes associated with TOR signaling.
Main Results:
- Identified 1927 upregulated genes in 34 functional modules related to transcriptional regulation, translation, hormone signaling, and homeostasis.
- TOR kinase emerged as a central regulatory hub, connected to three major axes: TOR-FKBP12-RPS6A (translation), TOR-CBP20 (transcription, hormone signaling, SE regulators), and TOR-TAP46 (metabolism, genome stability).
- Network analysis revealed 411 embryo-lethal genes, highlighting the importance of coordinated regulation during embryogenesis.
Conclusions:
- TOR signaling acts as an integrative hub, coordinating transcriptional, metabolic, translational, and genome-stability pathways during 2,4-D-induced SE.
- The identified TOR-associated interactome provides a framework for understanding SE regulatory mechanisms.
- This study offers potential molecular targets for enhancing plant regeneration and crop genetic engineering.
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