2019
DOI: 10.1371/journal.pone.0224429
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Transcriptional foliar profile of the C3-CAM bromeliad Guzmania monostachia

Abstract: Guzmania monostachia is an epiphytic tank bromeliad that displays the inducible CAM photosynthesis under stressful conditions and had the highest stomata density in the leaf apex, while the base portion has the highest density of trichomes, which are specialized structures used to acquire water and nutrients from the tank solution. In order to correlate the genetic factors behind these morpho-physiological characteristics along the leaf blade of G. monostachia, a comparative transcriptome analysis was performe… Show more

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Cited by 9 publications
(9 citation statements)
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“…In Guzmania monostachia, people found that the up-regulated genes of the leaf tip are mainly enriched in the regulation of stomatal movement, tryptophan metabolic process, chlorophyll biosynthetic process, and aspartate metabolic process. However, the up-regulated genes of leaf base are mainly related to response to water deprivation, starch, and sucrose metabolic processes [ 41 ]. These results are consistent with our findings, indicating that core CAM-related genes and steps between inducible and constitutive CAM plants are similar.…”
Section: Discussionmentioning
confidence: 99%
“…In Guzmania monostachia, people found that the up-regulated genes of the leaf tip are mainly enriched in the regulation of stomatal movement, tryptophan metabolic process, chlorophyll biosynthetic process, and aspartate metabolic process. However, the up-regulated genes of leaf base are mainly related to response to water deprivation, starch, and sucrose metabolic processes [ 41 ]. These results are consistent with our findings, indicating that core CAM-related genes and steps between inducible and constitutive CAM plants are similar.…”
Section: Discussionmentioning
confidence: 99%
“…Total RNA was extracted using the PureLink ® RNA Mini Kit (Ambion) according to the manufacturer's protocol. RNA concentration, quality, and integrity were checked as described in Mercier et al (2019). Samples with integrity number ≥6.5 were pooled to generate libraries using TruSeq RNA Sample Preparation Kit, Set A (Illumina Inc., United States).…”
Section: Rna Extraction Rna-seq De Novo Assembly Annotation and Analysismentioning
confidence: 99%
“…Samples with integrity number ≥6.5 were pooled to generate libraries using TruSeq RNA Sample Preparation Kit, Set A (Illumina Inc., United States). Paired-end sequences were generated as described by Mercier et al (2019), and only high-quality sequences (with average PhredScore over 24) were used. Sequence normalization and de novo transcriptome assembly were performed using Trinity (Grabherr et al, 2011;Haas et al, 2013) as described in Mercier et al (2019), and the reads were deposited at NCBI at the Bioproject ID PRJNA532595.…”
Section: Rna Extraction Rna-seq De Novo Assembly Annotation and Analysismentioning
confidence: 99%
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