4.7 Article

Gene expression profiling before and after internode culture for adventitious shoot formation in ipecac

Journal

BMC PLANT BIOLOGY
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12870-022-03756-w

Keywords

Adventitious shoot; Carapichea ipecacuanha; De novo transcriptome assembly; Internodal segment; RNA-seq; Transcriptional change

Categories

Funding

  1. Inoue Enryo Memorial Foundation for Promoting Science from Toyo University
  2. Japan Science Society [2022-4085]
  3. JST SPRING [JPMJSP2159]
  4. 30th and 31st Botanical Research Grant of Ichimura Foundation
  5. NIBB Collaborative Research Program [19-416, 20-418, 21-313, 22NIBB408]

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The study used RNA-seq analysis to compare gene expression patterns in apical and basal regions of internodal segments before and after a week of culture for adventitious shoot formation. The results identified 8987 differentially expressed genes, with 276 genes being upregulated in the apical region after culture. These genes include phytohormone-response and shoot-formation-related genes, as validated by quantitative real-time PCR assay.
Background In ipecac (Carapichea ipecacuanha (Brot.) L. Andersson), adventitious shoots can be induced simply by placing internodal segments on phytohormone-free culture medium. The shoots form locally on the epidermis of the apical region of the segments, but not the basal region. Levels of endogenous auxin and cytokinin transiently increase in the segments after 1 week of culture. Results Here, we conducted RNA-seq analysis to compare gene expression patterns in apical and basal regions of segments before culture and after 1 week of culture for adventitious shoot formation. The results revealed 8987 differentially expressed genes in a de novo assembly of 76,684 genes. Among them, 276 genes were upregulated in the apical region after 1 week of culture relative to before culture and the basal region after 1 week of culture. These genes include 18 phytohormone-response genes and shoot-formation-related genes. Validation of the gene expression by quantitative real-time PCR assay confirmed that the expression patterns were similar to those of the RNA-seq data. Conclusions The transcriptome data show that expression of cytokinin biosynthesis genes is induced along with the acquisition of cellular pluripotency and the initiation of cell division by wounding in the apical region of internodal segments, that trigger adventitious shoot formation without callusing.

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