Liu Rui, Liu Yinggao, Ye Nenghui, Zhu Guohui, Chen Moxian, Jia Liguo, Xia Yiji, Shi Lu, Jia Wensuo, Zhang Jianhua
College of Life Science, Shandong University, Jinan, Shandong, China Department of Biology, Hong Kong Baptist University, Hong Kong, China.
State Key Laboratory of Crop Biology, College of Life Science, Shandong Agricultural University, Taian, Shandong, China.
J Exp Bot. 2015 Mar;66(5):1339-53. doi: 10.1093/jxb/eru484. Epub 2014 Dec 24.
Dual-specificity protein phosphatases (DsPTPs) target both tyrosine and serine/threonine residues and play roles in plant growth and development. We have characterized an Arabidopsis mutant, dsptp1, which shows a higher seed germination rate and better root elongation under osmotic stress than the wild type. By contrast, its overexpression line, DsPTP1-OE, shows inhibited seed germination and root elongation; and its complemented line, DsPTP1-Com, resembles the wild type and rescues DsPTP1-OE under osmotic stress. Expression of AtDsPTP1 is enhanced by osmotic stress in seed coats, bases of rosette leaves, and roots. Compared with the wild type, the dsptp1 mutant shows increased proline accumulation, reduced malondialdehyde (MDA) content and ion leakage, and enhanced antioxidant enzyme activity in response to osmotic stress. AtDsPTP1 regulates the transcript levels of various dehydration-responsive genes under osmotic stress. Abscisic acid (ABA) accumulation in dsptp1 under osmotic stress is reduced with reduced expression of the ABA-biosynthesis gene NCED3 and increased expression of the ABA-catabolism gene CYP707A4. AtDsPTP1 also regulates the expression of key components in the ABA-signalling pathway. In conclusion, AtDsPTP1 regulates ABA accumulation, and acts as a negative regulator in osmotic stress signalling during Arabidospsis seed germination and seedling establishment.
双特异性蛋白磷酸酶(DsPTPs)作用于酪氨酸和丝氨酸/苏氨酸残基,在植物生长发育中发挥作用。我们对拟南芥突变体dsptp1进行了表征,该突变体在渗透胁迫下比野生型表现出更高的种子萌发率和更好的根伸长。相比之下,其过表达株系DsPTP1-OE表现出种子萌发和根伸长受到抑制;而其互补株系DsPTP1-Com与野生型相似,并在渗透胁迫下拯救了DsPTP1-OE。AtDsPTP1在种皮、莲座叶基部和根中受渗透胁迫诱导表达增强。与野生型相比,dsptp1突变体在渗透胁迫下脯氨酸积累增加、丙二醛(MDA)含量和离子渗漏减少,抗氧化酶活性增强。AtDsPTP1在渗透胁迫下调节各种脱水响应基因的转录水平。渗透胁迫下dsptp1中脱落酸(ABA)积累减少,ABA生物合成基因NCED3表达降低,ABA分解代谢基因CYP707A4表达增加。AtDsPTP1还调节ABA信号通路关键组分的表达。总之,AtDsPTP1调节ABA积累,并在拟南芥种子萌发和幼苗建立过程中的渗透胁迫信号传导中作为负调节因子发挥作用。