The wheat TdRL1 is the functional homolog of the rice RSS1 and promotes plant salt stress tolerance

被引:4
|
作者
Mahjoubi, Habib [1 ,2 ]
Tamari, Yutaka [3 ]
Takeda, Shin [3 ]
Bouchabke-Coussa, Oumaya [4 ]
Hanin, Moez [5 ]
Herzog, Etienne [2 ]
Schmit, Anne-Catherine [2 ]
Chaboute, Marie-Edith [2 ]
Ebel, Chantal [5 ]
机构
[1] Ctr Biotechnol Sfax, Lab Biotechnol & Ameliorat Plantes, BP 1177, Sfax 3018, Tunisia
[2] Univ Strasbourg, CNRS, UPR 2357, Inst Biol Mol Plantes, 12 Rue Gen Zimmer, F-67084 Strasbourg, France
[3] Nagoya Univ, Biosci & Biotechnol Ctr, Chikusa Ku, Nagoya, Aichi 4648601, Japan
[4] Univ Paris Saclay, AgroParisTech, Inst Jean Pierre Bourgin, INRA,CNRS, F-78000 Versailles, France
[5] Univ Sfax, Inst Biotechnol, Plant Physiol & Funct Genom Res Unit, BP 1175, Sfax 3038, Tunisia
关键词
Abiotic stress; Salt; RSS1; Durum wheat TdRL1; Cellular localization; Oxidative stress; AGROBACTERIUM-MEDIATED TRANSFORMATION; PROTEINS; VECTORS; SHUGOSHINS; PATRONUS; COHESION; GIP2; SET;
D O I
10.1007/s00299-018-2333-2
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Key messageRice rss1 complementation assays show that wheat TdRL1 and RSS1 are true functional homologs. TdRL1 over-expression in Arabidopsis conferred salt stress tolerance and alleviated ROS accumulation.AbstractPlants have developed highly flexible adaptive responses to their ever-changing environment, which are often mediated by intrinsically disordered proteins (IDP). RICE SALT SENSITIVE 1 and Triticum durum RSS1-Like 1 protein (TdRL1) are both IDPs involved in abiotic stress responses, and possess conserved D and DEN-Boxes known to be required for post-translational degradation by the APC/C-cdc20 cyclosome. To further understand their function, we performed a computational analysis to compare RSS1 and TdRL1 co-expression networks revealing common gene ontologies, among which those related to cell cycle progression and regulation of microtubule (MT) networks were over-represented. When over-expressed in Arabidopsis, TdRL1::GFP was present in dividing cells and more visible in cortical and endodermal cells of the Root Apical Meristem (RAM). Incubation with the proteasome inhibitor MG132 stabilized TdRL1::GFP expression in RAM cells showing a post-translational regulation. Moreover, immuno-cytochemical analyses of transgenic roots showed that TdRL1 was present in the cytoplasm and within the microtubular spindle of mitotic cells, while, in interphasic cells, it was rather restricted to the cytoplasm with a spotty pattern at the nuclear periphery. Interestingly in cells subjected to stress, TdRL1 was partly relocated into the nucleus. Moreover, TdRL1 transgenic lines showed increased germination rates under salt stress conditions as compared to wild type. This enhanced salt stress tolerance was associated to an alleviation of oxidative damage. Finally, when expressed in the rice rss1 mutant, TdRL1 suppressed its dwarf phenotype upon salt stress, confirming that both proteins are true functional homologs required for salt stress tolerance in cereals.
引用
收藏
页码:1625 / 1637
页数:13
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