» Articles » PMID: 30314311

Combinations of Small RNA, RNA, and Degradome Sequencing Uncovers the Expression Pattern of MicroRNA⁻mRNA Pairs Adapting to Drought Stress in Leaf and Root of L

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2018 Oct 14
PMID 30314311
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Drought stress is a global problem, and the lack of water is a key factor that leads to agricultural shortages. MicroRNAs play a crucial role in the plant drought stress response; however, the microRNAs and their targets involved in drought response have not been well elucidated. In the present study, we used Illumina platform (https://www.illumina.com/) and combined data from miRNA, RNA, and degradome sequencing to explore the drought- and organ-specific miRNAs in orchardgrass ( L.) leaf and root. We aimed to find potential miRNA⁻mRNA regulation patterns responding to drought conditions. In total, 519 (486 conserved and 33 novel) miRNAs were identified, of which, 41 miRNAs had significant differential expression among the comparisons ( < 0.05). We also identified 55,366 unigenes by RNA-Seq, where 12,535 unigenes were differently expressed. Finally, our degradome analysis revealed that 5950 transcripts were targeted by 487 miRNAs. A correlation analysis identified that miRNA and its target heat shock protein family A (HSP70) member 5 gene () may be essential in organ-specific plant drought stress response and/or adaptation in orchardgrass. Additionally, Gene ontology (GO) and Kyoto encyclopedia of genes and genomes (KEGG) analyses found that "antigen processing and presentation" was the most enriched downregulated pathway in adaptation to drought conditions. Taken together, we explored the genes and miRNAs that may be involved in drought adaptation of orchardgrass and identified how they may be regulated. These results serve as a valuable genetic resource for future studies focusing on how plants adapted to drought conditions.

Citing Articles

MicroRNAs in Plant Genetic Regulation of Drought Tolerance and Their Function in Enhancing Stress Adaptation.

Zhakypbek Y, Belkozhayev A, Kerimkulova A, Kossalbayev B, Murat T, Tursbekov S Plants (Basel). 2025; 14(3).

PMID: 39942972 PMC: 11820447. DOI: 10.3390/plants14030410.


Advanced Biotechnological Interventions in Mitigating Drought Stress in Plants.

Simsek O, Isak M, Donmez D, Dalda Sekerci A, Izgu T, Kacar Y Plants (Basel). 2024; 13(5).

PMID: 38475564 PMC: 10934033. DOI: 10.3390/plants13050717.


Transcriptome Profiling Provides Insights into the Early Development of Tiller Buds in High- and Low-Tillering Orchardgrass Genotypes.

Feng G, Xu X, Liu W, Hao F, Yang Z, Nie G Int J Mol Sci. 2023; 24(22).

PMID: 38003564 PMC: 10671593. DOI: 10.3390/ijms242216370.


Comparative transcriptomic analysis of the gene expression and underlying molecular mechanism of submergence stress response in orchardgrass roots.

Qu M, Zheng Y, Bi L, Yang X, Shang P, Zhou X Front Plant Sci. 2023; 13:1104755.

PMID: 36704155 PMC: 9871833. DOI: 10.3389/fpls.2022.1104755.


Molecular Aspects of MicroRNAs and Phytohormonal Signaling in Response to Drought Stress: A Review.

Ahmad H, Wang X, Ijaz M, Mahmood-Ur-Rahman , Oranab S, Ali M Curr Issues Mol Biol. 2022; 44(8):3695-3710.

PMID: 36005149 PMC: 9406886. DOI: 10.3390/cimb44080253.


References
1.
Voinnet O . Origin, biogenesis, and activity of plant microRNAs. Cell. 2009; 136(4):669-87. DOI: 10.1016/j.cell.2009.01.046. View

2.
Thiebaut F, Grativol C, Tanurdzic M, Carnavale-Bottino M, Vieira T, Romeiro Motta M . Differential sRNA regulation in leaves and roots of sugarcane under water depletion. PLoS One. 2014; 9(4):e93822. PMC: 3973653. DOI: 10.1371/journal.pone.0093822. View

3.
Ma D, Sun D, Wang C, Li Y, Guo T . Expression of flavonoid biosynthesis genes and accumulation of flavonoid in wheat leaves in response to drought stress. Plant Physiol Biochem. 2014; 80:60-6. DOI: 10.1016/j.plaphy.2014.03.024. View

4.
Wang J, Cheng G, Wang C, He Z, Lan X, Zhang S . The bHLH transcription factor CgbHLH001 is a potential interaction partner of CDPK in halophyte Chenopodium glaucum. Sci Rep. 2017; 7(1):8441. PMC: 5559460. DOI: 10.1038/s41598-017-06706-x. View

5.
Ji Y, Zhang X, Pen Y, Liang X, Huang L, Chen L . [Effects of drought stress on the root growth and photosynthetic characters of Dactylis glomerata seedlings]. Ying Yong Sheng Tai Xue Bao. 2014; 24(10):2763-9. View