Nguyen Yen Thi Hai, Nguyen Giang Thu, Nguyen Hung Duc, Vu Thuy Thi Thu, Nguyen Lan Thi Ngoc, Nguyen Quan Huu, Chu Mau Hoang
Thai Nguyen University of Sciences, Thai Nguyen, Viet Nam.
Pham Ngoc Thach University of Medicine, Ho Chi Minh City, Viet Nam.
Mol Biol Rep. 2025 Jun 30;52(1):656. doi: 10.1007/s11033-025-10767-x.
Salt stress is a significant challenge that disrupts soybean growth, development, yield, and quality. A few DREB genes in the soybean have been reported to activate downstream genes in response to abiotic stresses; however, the functions of many soybean DREB, including DREB5, remain uncharacterized. This study aimed to determine the expression of the GmDREB5 and its effects on the transcription of the NtP5CS and NtSODFe in tobacco's response to salt stress.
In this study, the construct containing the soybean GmDREB5 gene was transformed into tobacco, and the expression of GmDREB5 and its downstream genes was analyzed using real-time RT-PCR. The results showed that under salt stress, the transcription levels of GmDREB5, NtP5CS, and NtSODFe increased from 8.01-fold to 87.31-fold compared to wild-type (WT) and 4.12-fold to 4.77-fold compared to under no stress conditions. The TG08 line exhibited the highest transcription levels of these genes and proline content, 2.94-fold to 4.50-fold higher compared to the WT and under non-stress conditions. The analysis in silico molecular docking showed that the DNA binding sites of the AP2 region of the DREB transcription factor interacted with the cis-acting motifs, DRE/CRT, and GT-1 of the promoter, which regulate the NtP5CS and NtSODFe.
These findings indicate that overexpression of GmDREB5 could enhance the transcription of NtP5CS and NtSODFe, and the transcriptional activation mechanism of downstream genes was confirmed by the in silico molecular docking. This highlights GmDREB5 as a promising candidate for improving crop salt tolerance in response to salt stress.
盐胁迫是一个重大挑战,会干扰大豆的生长、发育、产量和品质。据报道,大豆中的一些DREB基因可响应非生物胁迫激活下游基因;然而,许多大豆DREB基因的功能,包括DREB5,仍未得到表征。本研究旨在确定GmDREB5在烟草响应盐胁迫中的表达及其对NtP5CS和NtSODFe转录的影响。
在本研究中,将含有大豆GmDREB5基因的构建体转化到烟草中,并使用实时RT-PCR分析GmDREB5及其下游基因的表达。结果表明,在盐胁迫下,与野生型(WT)相比,GmDREB5、NtP5CS和NtSODFe的转录水平提高了8.01倍至87.31倍,与非胁迫条件下相比提高了4.12倍至4.77倍。TG08株系这些基因的转录水平和脯氨酸含量最高,与WT相比以及在非胁迫条件下高2.94倍至4.50倍。计算机模拟分子对接分析表明,DREB转录因子AP2区域的DNA结合位点与启动子的顺式作用基序DRE/CRT和GT-1相互作用,后者调控NtP5CS和NtSODFe。
这些发现表明,GmDREB5的过表达可增强NtP5CS和NtSODFe的转录,并且通过计算机模拟分子对接证实了下游基因的转录激活机制。这突出了GmDREB5作为响应盐胁迫提高作物耐盐性的有前景的候选基因。