» Articles » PMID: 38392968

The Emerging Role of Non-Coding RNAs (ncRNAs) in Plant Growth, Development, and Stress Response Signaling

Overview
Journal Noncoding RNA
Date 2024 Feb 23
PMID 38392968
Authors
Affiliations
Soon will be listed here.
Abstract

Plant species utilize a variety of regulatory mechanisms to ensure sustainable productivity. Within this intricate framework, numerous non-coding RNAs (ncRNAs) play a crucial regulatory role in plant biology, surpassing the essential functions of RNA molecules as messengers, ribosomal, and transfer RNAs. ncRNAs represent an emerging class of regulators, operating directly in the form of small interfering RNAs (siRNAs), microRNAs (miRNAs), long noncoding RNAs (lncRNAs), and circular RNAs (circRNAs). These ncRNAs exert control at various levels, including transcription, post-transcription, translation, and epigenetic. Furthermore, they interact with each other, contributing to a variety of biological processes and mechanisms associated with stress resilience. This review primarily concentrates on the recent advancements in plant ncRNAs, delineating their functions in growth and development across various organs such as root, leaf, seed/endosperm, and seed nutrient development. Additionally, this review broadens its scope by examining the role of ncRNAs in response to environmental stresses such as drought, salt, flood, heat, and cold in plants. This compilation offers updated information and insights to guide the characterization of the potential functions of ncRNAs in plant growth, development, and stress resilience in future research.

Citing Articles

Bol-miR168a is a key regulator of defense responses to Sclerotinia sclerotiorum in Brassica oleracea.

Zha D, Raza M, Ye X, Song J Plant Cell Rep. 2025; 44(3):67.

PMID: 40014221 DOI: 10.1007/s00299-025-03451-8.


The importance of genotyping within the climate-smart plant breeding value chain - integrative tools for genetic enhancement programs.

Garcia-Oliveira A, Ortiz R, Sarsu F, Rasmussen S, Agre P, Asfaw A Front Plant Sci. 2025; 15:1518123.

PMID: 39980758 PMC: 11839310. DOI: 10.3389/fpls.2024.1518123.


Genome-Wide Identification of the miRNA Family and Exploration of Their Expression Characteristics Caused by the Replant Disease Formation-Related Principal Factor.

Gu L, Lai Y, Zhang G, Yang Y, Zhang B, Wang J Genes (Basel). 2024; 15(9).

PMID: 39336830 PMC: 11431045. DOI: 10.3390/genes15091239.


Advances in CircRNAs in the Past Decade: Review of CircRNAs Biogenesis, Regulatory Mechanisms, and Functions in Plants.

Zhang D, Ma Y, Naz M, Ahmed N, Zhang L, Zhou J Genes (Basel). 2024; 15(7).

PMID: 39062737 PMC: 11276256. DOI: 10.3390/genes15070958.

References
1.
Wang S, Sun X, Hoshino Y, Yu Y, Jia B, Sun Z . MicroRNA319 positively regulates cold tolerance by targeting OsPCF6 and OsTCP21 in rice (Oryza sativa L.). PLoS One. 2014; 9(3):e91357. PMC: 3965387. DOI: 10.1371/journal.pone.0091357. View

2.
Yang T, Wang Y, Teotia S, Wang Z, Shi C, Sun H . The interaction between miR160 and miR165/166 in the control of leaf development and drought tolerance in Arabidopsis. Sci Rep. 2019; 9(1):2832. PMC: 6391385. DOI: 10.1038/s41598-019-39397-7. View

3.
Kindgren P, Ard R, Ivanov M, Marquardt S . Transcriptional read-through of the long non-coding RNA SVALKA governs plant cold acclimation. Nat Commun. 2018; 9(1):4561. PMC: 6212407. DOI: 10.1038/s41467-018-07010-6. View

4.
Schommer C, Debernardi J, Bresso E, Rodriguez R, Palatnik J . Repression of cell proliferation by miR319-regulated TCP4. Mol Plant. 2014; 7(10):1533-44. DOI: 10.1093/mp/ssu084. View

5.
Zhao T, Tao X, Li M, Gao M, Chen J, Zhou N . Role of phasiRNAs from two distinct phasing frames of GhMYB2 loci in cis- gene regulation in the cotton genome. BMC Plant Biol. 2020; 20(1):219. PMC: 7227086. DOI: 10.1186/s12870-020-02430-3. View