A Two-Staged Model of Na+ Exclusion in Rice Explained by 3D Modeling of HKT Transporters and Alternative Splicing
The HKT family of Na(+) and Na(+)/K(+) transporters is implicated in plant salinity tolerance. Amongst these transporters, the cereal HKT1;4 and HKT1;5 are responsible for Na(+) exclusion from photosynthetic tissues, a key mechanism for plant salinity tolerance. It has been suggested that Na(+) is r...
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Published in | PloS one Vol. 7; no. 7; p. e39865 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Public Library of Science
11.07.2012
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Abstract | The HKT family of Na(+) and Na(+)/K(+) transporters is implicated in plant salinity tolerance. Amongst these transporters, the cereal HKT1;4 and HKT1;5 are responsible for Na(+) exclusion from photosynthetic tissues, a key mechanism for plant salinity tolerance. It has been suggested that Na(+) is retrieved from the xylem transpiration stream either in the root or the leaf sheath, protecting the leaf blades from excessive Na(+) accumulation. However, direct evidence for this scenario is scarce. Comparative modeling and evaluation of rice (Oryza sativa) HKT-transporters based on the recent crystal structure of the bacterial TrkH K(+) transporter allowed to reconcile transcriptomic and physiological data. For OsHKT1;5, both transcript abundance and protein structural features within the selectivity filter could control shoot Na(+) accumulation in a range of rice varieties. For OsHKT1;4, alternative splicing of transcript and the anatomical complexity of the sheath needed to be taken into account. Thus, Na(+) accumulation in a specific leaf blade seems to be regulated by abundance of a correctly spliced OsHKT1;4 transcript in a corresponding sheath. Overall, allelic variation of leaf blade Na(+) accumulation can be explained by a complex interplay of gene transcription, alternative splicing and protein structure. |
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AbstractList | The HKT family of Na(+) and Na(+)/K(+) transporters is implicated in plant salinity tolerance. Amongst these transporters, the cereal HKT1;4 and HKT1;5 are responsible for Na(+) exclusion from photosynthetic tissues, a key mechanism for plant salinity tolerance. It has been suggested that Na(+) is retrieved from the xylem transpiration stream either in the root or the leaf sheath, protecting the leaf blades from excessive Na(+) accumulation. However, direct evidence for this scenario is scarce. Comparative modeling and evaluation of rice (Oryza sativa) HKT-transporters based on the recent crystal structure of the bacterial TrkH K(+) transporter allowed to reconcile transcriptomic and physiological data. For OsHKT1;5, both transcript abundance and protein structural features within the selectivity filter could control shoot Na(+) accumulation in a range of rice varieties. For OsHKT1;4, alternative splicing of transcript and the anatomical complexity of the sheath needed to be taken into account. Thus, Na(+) accumulation in a specific leaf blade seems to be regulated by abundance of a correctly spliced OsHKT1;4 transcript in a corresponding sheath. Overall, allelic variation of leaf blade Na(+) accumulation can be explained by a complex interplay of gene transcription, alternative splicing and protein structure. The HKT family of Na(+) and Na(+)/K(+) transporters is implicated in plant salinity tolerance. Amongst these transporters, the cereal HKT1;4 and HKT1;5 are responsible for Na(+) exclusion from photosynthetic tissues, a key mechanism for plant salinity tolerance. It has been suggested that Na(+) is retrieved from the xylem transpiration stream either in the root or the leaf sheath, protecting the leaf blades from excessive Na(+) accumulation. However, direct evidence for this scenario is scarce. Comparative modeling and evaluation of rice (Oryza sativa) HKT-transporters based on the recent crystal structure of the bacterial TrkH K(+) transporter allowed to reconcile transcriptomic and physiological data. For OsHKT1;5, both transcript abundance and protein structural features within the selectivity filter could control shoot Na(+) accumulation in a range of rice varieties. For OsHKT1;4, alternative splicing of transcript and the anatomical complexity of the sheath needed to be taken into account. Thus, Na(+) accumulation in a specific leaf blade seems to be regulated by abundance of a correctly spliced OsHKT1;4 transcript in a corresponding sheath. Overall, allelic variation of leaf blade Na(+) accumulation can be explained by a complex interplay of gene transcription, alternative splicing and protein structure.The HKT family of Na(+) and Na(+)/K(+) transporters is implicated in plant salinity tolerance. Amongst these transporters, the cereal HKT1;4 and HKT1;5 are responsible for Na(+) exclusion from photosynthetic tissues, a key mechanism for plant salinity tolerance. It has been suggested that Na(+) is retrieved from the xylem transpiration stream either in the root or the leaf sheath, protecting the leaf blades from excessive Na(+) accumulation. However, direct evidence for this scenario is scarce. Comparative modeling and evaluation of rice (Oryza sativa) HKT-transporters based on the recent crystal structure of the bacterial TrkH K(+) transporter allowed to reconcile transcriptomic and physiological data. For OsHKT1;5, both transcript abundance and protein structural features within the selectivity filter could control shoot Na(+) accumulation in a range of rice varieties. For OsHKT1;4, alternative splicing of transcript and the anatomical complexity of the sheath needed to be taken into account. Thus, Na(+) accumulation in a specific leaf blade seems to be regulated by abundance of a correctly spliced OsHKT1;4 transcript in a corresponding sheath. Overall, allelic variation of leaf blade Na(+) accumulation can be explained by a complex interplay of gene transcription, alternative splicing and protein structure. The HKT family of Na + and Na + /K + transporters is implicated in plant salinity tolerance. Amongst these transporters, the cereal HKT1;4 and HKT1;5 are responsible for Na + exclusion from photosynthetic tissues, a key mechanism for plant salinity tolerance. It has been suggested that Na + is retrieved from the xylem transpiration stream either in the root or the leaf sheath, protecting the leaf blades from excessive Na + accumulation. However, direct evidence for this scenario is scarce. Comparative modeling and evaluation of rice (Oryza sativa) HKT-transporters based on the recent crystal structure of the bacterial TrkH K + transporter allowed to reconcile transcriptomic and physiological data. For OsHKT1;5, both transcript abundance and protein structural features within the selectivity filter could control shoot Na + accumulation in a range of rice varieties. For OsHKT1;4, alternative splicing of transcript and the anatomical complexity of the sheath needed to be taken into account. Thus, Na + accumulation in a specific leaf blade seems to be regulated by abundance of a correctly spliced OsHKT1;4 transcript in a corresponding sheath. Overall, allelic variation of leaf blade Na + accumulation can be explained by a complex interplay of gene transcription, alternative splicing and protein structure. |
Author | Hrmova, Maria Plett, Darren Shirley, Neil Tester, Mark Cotsaftis, Olivier |
AuthorAffiliation | United States Department of Agriculture, Agricultural Research Service, United States of America Australian Centre for Plant Functional Genomics, University of Adelaide, Adelaide, South Australia, Australia |
AuthorAffiliation_xml | – name: Australian Centre for Plant Functional Genomics, University of Adelaide, Adelaide, South Australia, Australia – name: United States Department of Agriculture, Agricultural Research Service, United States of America |
Author_xml | – sequence: 1 givenname: Olivier surname: Cotsaftis fullname: Cotsaftis, Olivier – sequence: 2 givenname: Darren surname: Plett fullname: Plett, Darren – sequence: 3 givenname: Neil surname: Shirley fullname: Shirley, Neil – sequence: 4 givenname: Mark surname: Tester fullname: Tester, Mark – sequence: 5 givenname: Maria surname: Hrmova fullname: Hrmova, Maria |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22808069$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | 2012 Cotsaftis et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Cotsaftis et al. 2012 |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Conceived and designed the experiments: OC DP NS MH. Performed the experiments: OC DP NS MH. Analyzed the data: OC. Contributed reagents/materials/analysis tools: NS MT MH. Wrote the paper: OC MT MH. Plant growth and salinity essay: DP OC. Radioactive fluxes: DP. Molecular biology: OC. Individual leaf experiment: OC. qRT-PCR and HPLC: NS. Protein modeling: MH. |
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Snippet | The HKT family of Na(+) and Na(+)/K(+) transporters is implicated in plant salinity tolerance. Amongst these transporters, the cereal HKT1;4 and HKT1;5 are... The HKT family of Na+ and Na+/K+ transporters is implicated in plant salinity tolerance. Amongst these transporters, the cereal HKT1;4 and HKT1;5 are... The HKT family of Na + and Na + /K + transporters is implicated in plant salinity tolerance. Amongst these transporters, the cereal HKT1;4 and HKT1;5 are... The HKT family of Na + and Na + /K + transporters is implicated in plant salinity tolerance. Amongst these transporters, the cereal HKT1;4 and HKT1;5 are... |
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SubjectTerms | Abiotic stress Abundance Accumulation Alleles Alternative Splicing Arabidopsis Biology Cation Transport Proteins - chemistry Cation Transport Proteins - genetics Cation Transport Proteins - metabolism Cellulose Cluster analysis Complexity Computer Science Crystal structure Crystallography, X-Ray Gene Expression Regulation, Plant Genes Genomes Genomics Ion Transport Leaves Modelling Models, Molecular Oryza - genetics Oryza - metabolism Oryza sativa Photosynthesis Plant Leaves - genetics Plant Leaves - metabolism Plant Proteins - chemistry Plant Proteins - genetics Plant Proteins - metabolism Plant Roots - genetics Plant Roots - metabolism Plant Shoots - genetics Plant Shoots - metabolism Potassium - metabolism Protein Conformation Protein Isoforms - chemistry Protein Isoforms - genetics Protein Isoforms - metabolism Protein structure Proteins Quantitative analysis RNA, Messenger - genetics RNA, Messenger - metabolism Salinity Salinity effects Salinity tolerance Salt-Tolerant Plants - genetics Salt-Tolerant Plants - metabolism Sodium - metabolism Symporters - chemistry Symporters - genetics Symporters - metabolism Three dimensional models Tissues Transcription Transpiration Xylem |
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Title | A Two-Staged Model of Na+ Exclusion in Rice Explained by 3D Modeling of HKT Transporters and Alternative Splicing |
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