» Articles » PMID: 30626336

Rice OsRH58, a Chloroplast DEAD-box RNA Helicase, Improves Salt or Drought Stress Tolerance in Arabidopsis by Affecting Chloroplast Translation

Overview
Journal BMC Plant Biol
Publisher Biomed Central
Specialty Biology
Date 2019 Jan 11
PMID 30626336
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Despite increasing characterization of DEAD-box RNA helicases (RHs) in chloroplast gene expression regulation at posttranscriptional levels in plants, their functional roles in growth responses of crops, including rice (Oryza sativa), to abiotic stresses are yet to be characterized. In this study, rice OsRH58 (LOC_Os01g73900), a chloroplast-localized DEAD-box RH, was characterized for its expression patterns upon stress treatment and its functional roles using transgenic Arabidopsis plants under normal and abiotic stress conditions.

Results: Chloroplast localization of OsRH58 was confirmed by analyzing the expression of OsRH58-GFP fusion proteins in tobacco leaves. Expression of OsRH58 in rice was up-regulated by salt, drought, or heat stress, whereas its expression was decreased by cold, UV, or ABA treatment. The OsRH58-expressing Arabidopsis plants were taller and had more seeds than the wild type under favorable conditions. The transgenic plants displayed faster seed germination, better seedling growth, and a higher survival rate than the wild type under high salt or drought stress. Importantly, levels of several chloroplast proteins were increased in the transgenic plants under salt or dehydration stress. Notably, OsRH58 harbored RNA chaperone activity.

Conclusions: These findings suggest that the chloroplast-transported OsRH58 possessing RNA chaperone activity confers stress tolerance by increasing translation of chloroplast mRNAs.

Citing Articles

Major components of RNAi gene families in cultivar : discovery and characterization.

Naim M, Alamin M, Mosharof M, Imtiaj A, Haque Mollah M Heliyon. 2024; 10(22):e40395.

PMID: 39624287 PMC: 11609679. DOI: 10.1016/j.heliyon.2024.e40395.


GWAS for Drought Resilience Traits in Red Clover ( L.).

Vleugels T, Ruttink T, Ariza-Suarez D, Dubey R, Saleem A, Roldan-Ruiz I Genes (Basel). 2024; 15(10).

PMID: 39457472 PMC: 11507065. DOI: 10.3390/genes15101347.


CRISPR/Cas9 mediated genome editing for crop improvement against Abiotic stresses: current trends and prospects.

Adane M, Alamnie G Funct Integr Genomics. 2024; 24(6):199.

PMID: 39453513 DOI: 10.1007/s10142-024-01480-2.


OsRH52A, a DEAD-box protein, regulates functional megaspore specification and is required for embryo sac development in rice.

Huang J, Qiao Z, Yu H, Lu Z, Chen W, Lu J J Exp Bot. 2024; 75(16):4802-4821.

PMID: 38642102 PMC: 11350083. DOI: 10.1093/jxb/erae180.


DEAD-Box RNA Helicase Family in Physic Nut ( L.): Structural Characterization and Response to Salinity.

da Silva R, Silva M, Ferreira-Neto J, Souza B, de Araujo F, Oliveira E Plants (Basel). 2024; 13(6).

PMID: 38592921 PMC: 10974417. DOI: 10.3390/plants13060905.


References
1.
Xia B, Ke H, Inouye M . Acquirement of cold sensitivity by quadruple deletion of the cspA family and its suppression by PNPase S1 domain in Escherichia coli. Mol Microbiol. 2001; 40(1):179-88. DOI: 10.1046/j.1365-2958.2001.02372.x. View

2.
Gallardo K, Job C, Groot S, Puype M, Demol H, Vandekerckhove J . Proteomic analysis of arabidopsis seed germination and priming. Plant Physiol. 2001; 126(2):835-48. PMC: 111173. DOI: 10.1104/pp.126.2.835. View

3.
Mohr S, Stryker J, Lambowitz A . A DEAD-box protein functions as an ATP-dependent RNA chaperone in group I intron splicing. Cell. 2002; 109(6):769-79. DOI: 10.1016/s0092-8674(02)00771-7. View

4.
Cordin O, Banroques J, Tanner N, Linder P . The DEAD-box protein family of RNA helicases. Gene. 2005; 367:17-37. DOI: 10.1016/j.gene.2005.10.019. View

5.
Vashisht A, Tuteja N . Stress responsive DEAD-box helicases: a new pathway to engineer plant stress tolerance. J Photochem Photobiol B. 2006; 84(2):150-60. DOI: 10.1016/j.jphotobiol.2006.02.010. View