Expression profiling of water stress responsive miroRNAs in banana (Musa spp.)
By: Amal Mohamud Naushad.
Contributor(s): K B Soni (Guide).
Material type:
Item type | Current location | Collection | Call number | Status | Date due | Barcode |
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KAU Central Library, Thrissur Theses | Reference Book | 660.6 AMA/EX PG (Browse shelf) | Not For Loan | 175430 |
MSc
The study entitled “Expression profiling of water stress responsive
microRNAs in Banana (Musa spp)” was conducted during 2019-2021, in the
Department of Plant Biotechnology, College of Agriculture, Vellayani. The study
envisaged expression profiling of selected computationally predicted miRNAs in
banana cultivar Nendran (Musa AAB) under water stress conditions.
Fifty-two novel miRNAs and their targets have been computationally predicted
in banana genome A, using NOVOMIR (Mathew, 2018) in a previous study conducted
in the Department of Plant Biotechnology. Among five miRNAs were selected in this
study for their validation and identifying their association with water stress response.
The microRNAs selected are miR-3900-5p (target: Heat shock protein, HSP gene),
miR-2172-5p (target: Putative Ethylene Responsive Transcription factor 1 (ERT)
gene), miR-971-5p (target: Argonaute, (ARG) gene, miR-6928-5p (target: FADdependent oxidoreductase gene), and miR-2172-5p (target: Diacylglycerol, DAG
gene).
Six months old in-vitro raised banana plants of cv. Nendran (Musa AAB) were
used in this study. Water stress was induced in the potted plants by withholding
irrigation for seven consecutive days. After 7 days, the relative water content in the leaf
samples was reduced from 93.84 to 59.32, indicating water stress.
The expression profile of the miRNAs and their target genes in banana plants
under water stress conditions was analysed by performing Real-time quantitative PCR
(RT-qPCR). Total RNA was extracted from leaf samples using the modified RodriguesGarcia method and reverse transcribed to cDNA using the miRNA specific stem-loop
primers designed. Selected miRNAs were amplified using miRNA specific forward and
universal reverse primers. The target genes were also amplified by designing primers.
The specificity of the primers was determined using a melt curve analysis. All the
reactions are conducted with three biological and two technical replicates.
Out of the four, three miRNAs (miR-2172-5p, miR-6928-5p and miR-971-
5p) and their target genes showed amplification in all the samples. All the water stressed
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plants showed upregulation of miR-2712-5p (4 to 11fold), and downregulation of
miR971-5p (0.1 to 0.4fold) and miR-6928-5p (0.2 to 0.7fold).
The two targets of miR2712-5p showed differential expression under the water
stressed conditions, DAG gene was downregulated (0.1 to 0.2folds) and ERT gene was
upregulated (2 to 3folds). Expression of FAD dependant oxidorductase (The target of
miR-6928-5p) and ARG (the target of miR971-5p) was increased up to 3 to 4folds
respectively in water stress conditions.
Relative gene expression analysis in the water-stressed plants indicated an
inverse correlation between all the three miRNAs and their targets, suggesting their
strong miRNA: target relation.
The study showed that miR-2172-5p, miR-971-5p, miR-6928-5p are water
stress-responsive in banana cv. Nendran. Since the products of all the target genes are
related to stress responses in plants, an in-depth study of these miRNAs may help
develop strategies for water stress management in bananas.
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