Liu Wenqing, Li Peng, Wang Xiu, Zhang Zhongxing, Wang Yanxiu
College of Horticulture, Gansu Agricultural University, Lanzhou 730070, China.
Plants (Basel). 2024 Jun 29;13(13):1803. doi: 10.3390/plants13131803.
Saline-alkali stress is a significant abiotic stress that restricts plant growth globally. Basic region leucine zipper () transcription factor proteins are widely involved in plants in response to abiotic stress such as saline-alkali stress. Based on transcriptome and quantitative real-time PCR (qRT-PCR), we found that the gene could respond to saline-alkali stress. Despite this discovery, the underlying mechanism by which the transcription factor responds to saline-alkaline stress remains unexplored. To address this gap in knowledge, we successfully cloned the (MD05G1121500) gene from for heterologous expression in , facilitating the investigation of its functional role in stress response. Compared to the wild type (WT), plants demonstrated enhanced growth and a lower degree of wilting when subjected to saline-alkali stress. Furthermore, several physiological indices of the plants altered under such stress conditions. The transgenic plants (OE-5, 6, and 8), which grew normally, exhibited a higher chlorophyll content and had greater root length in comparison to the control check (CK). effectively regulated the levels of the osmoregulatory substance proline (Pro), enhanced the activities of antioxidant enzymes such as peroxidase (POD) and superoxide dismutase (SOD), and reduced the levels of malondialdehyde (MDA) and relative conductivity (REC). These actions improved the ability of plant cells in transgenic to counteract ROS, as evidenced by the decreased accumulation of O and hydrogen peroxide (HO). In summary, the gene demonstrated effectiveness in alleviating saline-alkali stress in , presenting itself as an outstanding resistance gene for apples to combat saline-alkali stress.
盐碱胁迫是一种严重的非生物胁迫,在全球范围内限制植物生长。碱性区域亮氨酸拉链(bZIP)转录因子蛋白广泛参与植物对盐碱胁迫等非生物胁迫的响应。基于转录组和定量实时PCR(qRT-PCR),我们发现Md05G1121500基因可响应盐碱胁迫。尽管有这一发现,但bZIP转录因子响应盐碱胁迫的潜在机制仍未得到探索。为填补这一知识空白,我们成功从苹果中克隆了Md05G1121500基因,用于在拟南芥中进行异源表达,便于研究其在胁迫响应中的功能作用。与野生型(WT)相比,转基因拟南芥在遭受盐碱胁迫时生长增强且萎蔫程度较低。此外,在这种胁迫条件下,植物的几个生理指标发生了变化。正常生长的转基因拟南芥植株(OE-5、6和8)与对照(CK)相比,叶绿素含量更高,根长更长。Md05G1121500有效调节了渗透调节物质脯氨酸(Pro)的水平,增强了过氧化物酶(POD)和超氧化物歧化酶(SOD)等抗氧化酶的活性,并降低了丙二醛(MDA)和相对电导率(REC)的水平。这些作用提高了转基因拟南芥植物细胞对抗活性氧的能力,这一点从超氧阴离子(O₂⁻)和过氧化氢(H₂O₂)积累的减少得到证明。总之,Md05G1121500基因在减轻苹果的盐碱胁迫方面表现出有效性,是苹果对抗盐碱胁迫出色的抗性基因。