Ndosomal localization. The mutant lacking the EH domain behaves like an

Ndosomal localization. The mutant lacking the EH domain behaves like an EHD1 knock-down while the mutant lacking the coiled-coil domain behaves similarly to EHD1 overexpressing seedlings. This would suggest that the relative salt tolerance conferred by EHD1 may require intact localization and/or recycling function of the protein. One optional mechanism may be increased salt clearance in seedlings possessing increased recycling levels; simplistically, it 18325633 is possible that proteins in charge of salt clearance are able to function more rapidly. Vesicle trafficking seems to be involved in salt tolerance. As in the case of our EHD1 Knock-down seedlings, the Arabidopsis mutant tno-1 displays delayed formation of BFA bodies and increased sensitivity to salt stress [55]. TNO1 is a SNARE binding protein involved in vacuolar trafficking and salt tolerance, potentially via roles in vesicle fusion and in maintaining TGN structure or identity.We demonstrate here that plant EHD1 is an endocytic recycling protein; similar to what was reported for EHD1 in other organisms. The EH domain appears to be crucial for this function. Research into plant recycling is still in its infancy and additional advances are required before the exact pathway of recycling in which EHD1 functions can be elucidated. The involvement of EHD1 in salt tolerance may open new avenues for improving salinity tolerance by specifically modifying EHD1 expression and/ or recycling mechanisms, as they become elucidated.Materials and Methods Plant and cell culture material and growth conditionsNicotiana benthamiana and Arabidopsis thaliana cv Columbia were grown from seeds under greenhouse conditions. Transgenic plants were either germinated on the appropriate sterile selective solid media and transferred to soil 2? weeks after germination, or, for imaging, were germinated upright in desired media containing 0.8 plant agar.VectorsAtEHD1 was cloned in the sense orientation upstream of the GFP gene into the binary vector pBINPLUS between the 35S-VFigure 5. Effect of salt treatment on seed germination. Arabidopsis seeds were gereminated on 200 mM NaCl. ML-240 chemical information germination was normalized based on the germination values on media without NaCl. Values represent mean 6 SE of 6 experiments. doi:10.1371/journal.pone.0054533.gEHD1 Function AnalysisFigure 8. Viability of Arabidopsis seedlings treated with NaCl. Seedlings were floated on a 200 mM NaCl solution for 24 hours and then stained for viability with Neutral red. Values represent mean 6 SE of 4 experiments. doi:10.1371/journal.pone.0054533.gThe truncation mutants were generated by amplifying fragments of the cDNA as desired, with the following primers: EHD1_DEH FOR: 59atgcttattagcgatgttg (used with the EHD1 reverse primer); EHD1 DCC(1) REV: CATTATCGCTGGCATCTCC (used with the EHD1 forward primer to generate the first fragment); EHD1-DCC(2) FOR: TTTGGAAAGGTACAAAGAG (used with the EHD1 reverse primer to generate the second fragment; the fragments were then ligated to form EHD1 DCC); In addition to the forward and reverse primers disclosed in [25]. All constructs were cloned in pBINPLUS as described above for AtEHD1. The constructs were electroporated into Agrobacterium tumefaciens GV3101 and the bacteria used for transient expression assays. The Wave lines constructs were 478-01-3 site obtained from Prof. Geldner [37].Stable and transient transformationArabidopsis plants were transformed as previously described [58]. Transient expression was performed as previously d.Ndosomal localization. The mutant lacking the EH domain behaves like an EHD1 knock-down while the mutant lacking the coiled-coil domain behaves similarly to EHD1 overexpressing seedlings. This would suggest that the relative salt tolerance conferred by EHD1 may require intact localization and/or recycling function of the protein. One optional mechanism may be increased salt clearance in seedlings possessing increased recycling levels; simplistically, it 18325633 is possible that proteins in charge of salt clearance are able to function more rapidly. Vesicle trafficking seems to be involved in salt tolerance. As in the case of our EHD1 Knock-down seedlings, the Arabidopsis mutant tno-1 displays delayed formation of BFA bodies and increased sensitivity to salt stress [55]. TNO1 is a SNARE binding protein involved in vacuolar trafficking and salt tolerance, potentially via roles in vesicle fusion and in maintaining TGN structure or identity.We demonstrate here that plant EHD1 is an endocytic recycling protein; similar to what was reported for EHD1 in other organisms. The EH domain appears to be crucial for this function. Research into plant recycling is still in its infancy and additional advances are required before the exact pathway of recycling in which EHD1 functions can be elucidated. The involvement of EHD1 in salt tolerance may open new avenues for improving salinity tolerance by specifically modifying EHD1 expression and/ or recycling mechanisms, as they become elucidated.Materials and Methods Plant and cell culture material and growth conditionsNicotiana benthamiana and Arabidopsis thaliana cv Columbia were grown from seeds under greenhouse conditions. Transgenic plants were either germinated on the appropriate sterile selective solid media and transferred to soil 2? weeks after germination, or, for imaging, were germinated upright in desired media containing 0.8 plant agar.VectorsAtEHD1 was cloned in the sense orientation upstream of the GFP gene into the binary vector pBINPLUS between the 35S-VFigure 5. Effect of salt treatment on seed germination. Arabidopsis seeds were gereminated on 200 mM NaCl. Germination was normalized based on the germination values on media without NaCl. Values represent mean 6 SE of 6 experiments. doi:10.1371/journal.pone.0054533.gEHD1 Function AnalysisFigure 8. Viability of Arabidopsis seedlings treated with NaCl. Seedlings were floated on a 200 mM NaCl solution for 24 hours and then stained for viability with Neutral red. Values represent mean 6 SE of 4 experiments. doi:10.1371/journal.pone.0054533.gThe truncation mutants were generated by amplifying fragments of the cDNA as desired, with the following primers: EHD1_DEH FOR: 59atgcttattagcgatgttg (used with the EHD1 reverse primer); EHD1 DCC(1) REV: CATTATCGCTGGCATCTCC (used with the EHD1 forward primer to generate the first fragment); EHD1-DCC(2) FOR: TTTGGAAAGGTACAAAGAG (used with the EHD1 reverse primer to generate the second fragment; the fragments were then ligated to form EHD1 DCC); In addition to the forward and reverse primers disclosed in [25]. All constructs were cloned in pBINPLUS as described above for AtEHD1. The constructs were electroporated into Agrobacterium tumefaciens GV3101 and the bacteria used for transient expression assays. The Wave lines constructs were obtained from Prof. Geldner [37].Stable and transient transformationArabidopsis plants were transformed as previously described [58]. Transient expression was performed as previously d.