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Genome-wide Identification, Phylogenetic and Expression Pattern Analysis of HSF Family Genes in the Rye (Secale Cereale L.)

Overview
Journal BMC Plant Biol
Publisher Biomed Central
Specialty Biology
Date 2023 Sep 19
PMID 37726665
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Abstract

Background: Heat shock factor (HSF), a typical class of transcription factors in plants, has played an essential role in plant growth and developmental stages, signal transduction, and response to biotic and abiotic stresses. The HSF genes families has been identified and characterized in many species through leveraging whole genome sequencing (WGS). However, the identification and systematic analysis of HSF family genes in Rye is limited.

Results: In this study, 31 HSF genes were identified in Rye, which were unevenly distributed on seven chromosomes. Based on the homology of A. thaliana, we analyzed the number of conserved domains and gene structures of ScHSF genes that were classified into seven subfamilies. To better understand the developmental mechanisms of ScHSF family during evolution, we selected one monocotyledon (Arabidopsis thaliana) and five (Triticum aestivum L., Hordeum vulgare L., Oryza sativa L., Zea mays L., and Aegilops tauschii Coss.) specific representative dicotyledons associated with Rye for comparative homology mapping. The results showed that fragment replication events modulated the expansion of the ScHSF genes family. In addition, interactions between ScHSF proteins and promoters containing hormone- and stress-responsive cis-acting elements suggest that the regulation of ScHSF expression was complex. A total of 15 representative genes were targeted from seven subfamilies to characterize their gene expression responses in different tissues, fruit developmental stages, three hormones, and six different abiotic stresses.

Conclusions: This study demonstrated that ScHSF genes, especially ScHSF1 and ScHSF3, played a key role in Rye development and its response to various hormones and abiotic stresses. These results provided new insights into the evolution of HSF genes in Rye, which could help the success of molecular breeding in Rye.

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References
1.
Bartlomiej S, Justyna R, Ewa N . Bioactive compounds in cereal grains - occurrence, structure, technological significance and nutritional benefits - a review. Food Sci Technol Int. 2012; 18(6):559-68. DOI: 10.1177/1082013211433079. View

2.
Fan Y, Yan J, Lai D, Yang H, Xue G, He A . Genome-wide identification, expression analysis, and functional study of the GRAS transcription factor family and its response to abiotic stress in sorghum [Sorghum bicolor (L.) Moench]. BMC Genomics. 2021; 22(1):509. PMC: 8259154. DOI: 10.1186/s12864-021-07848-z. View

3.
Scharf K, Rose S, Zott W, Schoffl F, Nover L, Schoff F . Three tomato genes code for heat stress transcription factors with a region of remarkable homology to the DNA-binding domain of the yeast HSF. EMBO J. 1990; 9(13):4495-501. PMC: 552242. DOI: 10.1002/j.1460-2075.1990.tb07900.x. View

4.
Shabalina S, Ogurtsov A, Spiridonov A, Novichkov P, Spiridonov N, Koonin E . Distinct patterns of expression and evolution of intronless and intron-containing mammalian genes. Mol Biol Evol. 2010; 27(8):1745-9. PMC: 2908711. DOI: 10.1093/molbev/msq086. View

5.
Del Campo E, Casano L, Barreno E . Evolutionary implications of intron-exon distribution and the properties and sequences of the RPL10A gene in eukaryotes. Mol Phylogenet Evol. 2012; 66(3):857-67. DOI: 10.1016/j.ympev.2012.11.013. View