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Transcriptome Analysis Reveals the Effect of Propyl Gallate on Kiwifruit Callus Formation

Overview
Journal Plant Cell Rep
Publisher Springer
Date 2024 Feb 9
PMID 38334781
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Abstract

Exploring the potential action mechanisms of reactive oxygen species during the callus inducing, they can activate specific metabolic pathways in explants to regulate callus development. Reactive oxygen species (ROS) play an important role in the regulation of plant growth and development, but the mechanism of their action on plant callus formation remains to be elucidated. To address this question, kiwifruit was selected as the explant for callus induction, and the influence of ROS on callus formation was investigated by introducing propyl gallate (PG) as an antioxidant into the medium used for inducing callus. The results have unveiled that the inclusion of PG in the medium has disturbed the equilibrium of ROS during the formation of the kiwifruit callus. We selected the callus that was induced by the addition of 0.05 mmol/L PG to the MS medium. The callus exhibited a significant difference in the amount compared to the control medium without PG. The callus induced by the MS medium without PG was used as the control for comparison. KEGG enrichment indicated that PG exposure resulted in significant differences in gene expression in related pathways, such as phytohormone signaling and glutathione in kiwifruit callus. Weighted gene co-expression analysis indicated that the pertinent regulatory networks of both ROS and phytohormone signaling were critical for the establishment of callus in kiwifruit leaves. In addition, during the process of callus establishment, the ROS level of the explants was also closely related to the genes for transmembrane transport of substances, cell wall formation, and plant organ establishment. This investigation expands the theory of ROS-regulated callus formation and presents a new concept for the expeditious propagation of callus in kiwifruit.

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References
1.
Altpeter F, Springer N, Bartley L, Blechl A, Brutnell T, Citovsky V . Advancing Crop Transformation in the Era of Genome Editing. Plant Cell. 2016; 28(7):1510-20. PMC: 4981132. DOI: 10.1105/tpc.16.00196. View

2.
Atta R, Laurens L, Boucheron-Dubuisson E, Guivarch A, Carnero E, Giraudat-Pautot V . Pluripotency of Arabidopsis xylem pericycle underlies shoot regeneration from root and hypocotyl explants grown in vitro. Plant J. 2008; 57(4):626-44. DOI: 10.1111/j.1365-313X.2008.03715.x. View

3.
Birnbaum K, Roudier F . Epigenetic memory and cell fate reprogramming in plants. Regeneration (Oxf). 2017; 4(1):15-20. PMC: 5350078. DOI: 10.1002/reg2.73. View

4.
Che P, Lall S, Howell S . Developmental steps in acquiring competence for shoot development in Arabidopsis tissue culture. Planta. 2007; 226(5):1183-94. DOI: 10.1007/s00425-007-0565-4. View

5.
Chen S, Zhou Y, Chen Y, Gu J . fastp: an ultra-fast all-in-one FASTQ preprocessor. Bioinformatics. 2018; 34(17):i884-i890. PMC: 6129281. DOI: 10.1093/bioinformatics/bty560. View