Functional and regulatory diversity of homeobox-leucine zipper transcription factors BnaHB6 under dehydration and salt stress in Brassica napus L.

被引:0
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作者
Zyla, Natalia [1 ]
Ciesla, Agata [2 ]
Szala, Laurencja [3 ]
Babula-Skowronska, Danuta [1 ]
机构
[1] Polish Acad Sci, Inst Plant Genet, Strzeszynska 34, PL-60479 Poznan, Poland
[2] Adam Mickiewicz Univ, Inst Mol Biol & Biotechnol, Fac Biol, Lab Biotechnol, Poznan, Poland
[3] Natl Res Inst Radzikow, Plant Breeding & Acclimatizat Inst, Dept Oilseed Crops, Poznan Div, Strzeszynska 36, PL-60479 Poznan, Poland
关键词
HD-Zip I subfamily; BnaHB6; homologues; Abiotic stress; Circadian rhythm; Functional divergence; Brassica napus; CLASS-I; ARABIDOPSIS-THALIANA; EXPRESSION PROFILE; WATER-DEFICIT; GENE FAMILY; DNA-BINDING; PROTEIN; EVOLUTION; RESPONSES; ATHB-1;
D O I
10.1007/s11103-024-01465-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The plant-specific homeodomain-leucine zipper I subfamily is involved in the regulation of various biological processes, particularly growth, development and stress response. In the present study, we characterized four BnaHB6 homologues from Brassica napus. All BnaHB6 proteins have transcriptional activation activity. Structural and functional data indicate the complex role of BnaHB6 genes in regulating biological processes, with some functions conserved and others diverged. Transcriptional analyzes revealed that they are induced in a similar manner in different tissues but show different expression patterns in response to stress and circadian rhythm. Only the BnaA09HB6 and BnaC08HB6 genes are expressed under dehydration and salt stress, and in darkness. The partial transcriptional overlap of BnaHB6s with the evolutionarily related genes BnaHB5 and BnaHB16 was also observed. Transgenic Arabidopsis thaliana plants expressing a single proBnaHB6::GUS partially confirmed the expression results. Bioinformatic analysis allowed the identification of TF-binding sites in the BnaHB6 promoters that may control their expression under stress and circadian rhythm. ChIP-qPCR analysis revealed that BnaA09HB6 and BnaC08HB6 bind directly to the promoters of the target genes BnaABF4 and BnaDREB2A. Comparison of their expression patterns in the WT plants and the bnac08hb6 mutant showed that BnaC08HB6 positively regulates the expression of the BnaABF4 and BnaDREB2A genes under dehydration and salt stress. We conclude that four BnaHB6 homologues have distinct functions in response to stress despite high sequence similarity, possibly indicating different binding preferences with BnaABF4 and BnaDREB2A. We hypothesize that BnaC08HB6 and BnaA09HB6 function in a complex regulatory network under stress.
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页数:17
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