Yang Ce, Lu Xiang, Du Dan, Liang Zhongyi, Li Cheng, Hu Kang, Wang Hongjie, Cheng Yanbo, Lian Tengxiang, Nian Hai, Ma Qibin
The State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, South China Agricultural University, Guangzhou, Guangdong, 510642, China.
Key Laboratory of Plant Molecular Breeding of Guangdong Province, College of Agriculture, South China Agricultural University, Guangzhou, Guangdong, 510642, China.
BMC Plant Biol. 2024 Dec 26;24(1):1251. doi: 10.1186/s12870-024-06004-5.
MYB transcription factors (TFs) play crucial roles in the response to diverse abiotic and biotic stress factors in plants. In this study, the GsMYB10 gene encoding a MYB-CC transcription factor was cloned from wild soybean BW69 line. However, there is less report on the aluminum (Al)-tolerant gene in this subfamily.
The GsMYB10 gene was up-regulated by acidic aluminum stress and rich in the roots with a constitutive expression pattern in soybean. It was found that GsMYB10 protein contains the MYB and coiled-coil (CC) domains, localizes in the nucleus and holds transcriptional activity. The analysis of the transgenic phenotype revealed that the taproot length and root fresh weights of the GsMYB10-OE plants were greater than those of the wild type when subjected to AlCl treatments. While the accumulation of Al in root tip of GsMYB10 transgenic plants (59.37 ± 3.59 µg/g) significantly reduced compared with that of wild type (80.40 ± 3.16 µg/g) which were shallowly stained by hematoxylin under the treatments of AlCl. Physiological indexes showed that the proline content significantly increased 39-45% and the malondialdehyde content significantly reduced 37-42% in GsMYB10-OE plants compared with that of wild type. Transcriptomic analysis showed that overexpression of GsMYB10 induced a large number of differentially expressed genes (DEGs) with Al-treatment, which were related to wall modification related genes included PGs (such as Glyma.19g006200, Glyma.05g005800), XTHs (such as Glyma.12g080100, Glyma.12g101800, Glyma.08g093900 and Glyma.13g322500), NRAMPs and ABCs.
In summary, the data presented in this paper indicate that GsMYB10, as a new soybean MYB-CC TF, is a positive regulator and increases the adaptability of soybeans to acidic aluminum stress. The findings will contribute to the understanding of soybean response to acidic aluminum stress.
MYB转录因子在植物对多种非生物和生物胁迫因子的响应中发挥关键作用。在本研究中,从野生大豆BW69品系中克隆了编码MYB-CC转录因子的GsMYB10基因。然而,关于该亚家族中耐铝基因的报道较少。
GsMYB10基因在酸性铝胁迫下上调,在大豆根系中丰富且呈组成型表达模式。发现GsMYB10蛋白包含MYB和卷曲螺旋(CC)结构域,定位于细胞核并具有转录活性。转基因表型分析表明,在AlCl处理下,GsMYB10-OE植株的主根长度和根鲜重均大于野生型。在AlCl处理下,GsMYB10转基因植株根尖中铝的积累量(59.37±3.59μg/g)与野生型(80.40±3.16μg/g)相比显著降低,野生型经苏木精浅染色。生理指标显示,与野生型相比,GsMYB-10-OE植株中脯氨酸含量显著增加39-45%,丙二醛含量显著降低37-42%。转录组分析表明,GsMYB10的过表达在铝处理下诱导了大量差异表达基因(DEG),这些基因与细胞壁修饰相关基因有关,包括多聚半乳糖醛酸酶(PGs,如Glyma.19g006200、Glyma.05g005800)、木葡聚糖内转糖基酶/水解酶(XTHs,如Glyma.12g080100、Glyma.12g101800、Glyma.08g093900和Glyma.13g322500)、天然抗性相关巨噬细胞蛋白(NRAMPs)和ATP结合盒转运蛋白(ABCs)。
综上所述,本文数据表明GsMYB10作为一种新的大豆MYB-CC转录因子,是一种正向调控因子,可提高大豆对酸性铝胁迫的适应性。这些发现将有助于理解大豆对酸性铝胁迫的响应。