Yao Luming, Jiang Yina, Lu Xinxin, Wang Biao, Zhou Pei, Wu Tianlong
School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai, China.
Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai, China.
Mol Biol Rep. 2016 Oct;43(10):1089-100. doi: 10.1007/s11033-016-4042-7. Epub 2016 Jul 20.
Few regulators for drought tolerance have been identified in Lablab purpureus which is a multipurpose leguminous crop. The transcription factor MYB is involved in regulatory networks in response to abiotic and biotic stresses in plants. A novel R2R3-MYB factor in L. purpureus has been identified. An suppression subtraction hybridization (SSH) library was constructed using root tissues of L. purpureus MEIDOU 2012 from well-watered and water-stress treatments that were subjected to drought stress for 10 days. In addition, the cDNA of LpMYB1 was identified based on the SSH library. The cDNA of LpMYB1 is 858 bp and encodes a 285-amino acid protein with a calculated mass of 33.4 kDa. The LpMYB1 protein localizes to the nucleus and has transactivation activity with the activation domain in the C terminal region of the protein. In LpMYB1 overexpressed Arabidopsis, the tolerance of transgenic seedlings to drought and salt was improved, and the germination potential of transgenic seeds increase in the presence of NaCl or ABA. LpMYB1 is a drought-responsive R2R3-MYB factor that can increase the drought and salt tolerance of LpMYB1-overexpressed Arabidopsis.
作为一种多用途豆科作物,在豆科豇豆中,很少有耐旱调节因子被鉴定出来。转录因子MYB参与植物对非生物和生物胁迫的调控网络。在豆科豇豆中已鉴定出一种新型R2R3-MYB因子。利用在水分充足和水分胁迫处理下经受10天干旱胁迫的豆科豇豆“美豆2012”的根组织构建了一个抑制性消减杂交(SSH)文库。此外,基于SSH文库鉴定出了LpMYB1的cDNA。LpMYB1的cDNA为858 bp,编码一个285个氨基酸的蛋白质,计算分子量为33.4 kDa。LpMYB1蛋白定位于细胞核,并且在该蛋白质C末端区域具有转录激活活性。在过表达LpMYB1的拟南芥中,转基因幼苗对干旱和盐的耐受性提高了,并且在存在NaCl或ABA的情况下转基因种子的发芽势增加。LpMYB1是一种干旱响应型R2R3-MYB因子,可提高过表达LpMYB1的拟南芥的耐旱性和耐盐性。