Vacuolar Sulfate Transporters Are Essential Determinants Controlling Internal Distribution of Sulfate in Arabidopsis

التفاصيل البيبلوغرافية
العنوان: Vacuolar Sulfate Transporters Are Essential Determinants Controlling Internal Distribution of Sulfate in Arabidopsis
المؤلفون: Akiko Watanabe-Takahashi, Peter Buchner, Tomoyuki Yamaya, Tetsuro Mimura, Tatsuhiko Kataoka, Miwa Ohnishi, Naomi Hayashi, Hideki Takahashi, Malcolm J. Hawkesford
المصدر: The Plant Cell. 16:2693-2704
بيانات النشر: Oxford University Press (OUP), 2004.
سنة النشر: 2004
مصطلحات موضوعية: Molecular Sequence Data, Arabidopsis, chemistry.chemical_element, Plant Science, Vacuole, chemistry.chemical_compound, Arabidopsis thaliana, Sulfate, Research Articles, DNA Primers, Base Sequence, biology, Sulfates, Membrane Transport Proteins, Xylem, Cell Biology, Plants, Genetically Modified, biology.organism_classification, Sulfur, Cell biology, chemistry, Biochemistry, Sulfate Transporters, Cytoplasm, Vacuoles, Efflux
الوصف: Uptake of external sulfate from the environment and use of internal vacuolar sulfate pools are two important aspects of the acquisition of sulfur for metabolism. In this study, we demonstrated that the vacuolar SULTR4-type sulfate transporter facilitates the efflux of sulfate from the vacuoles and plays critical roles in optimizing the internal distribution of sulfate in Arabidopsis thaliana. SULTR4;1-green fluorescent protein (GFP) and SULTR4;2-GFP fusion proteins were expressed under the control of their own promoters in transgenic Arabidopsis. The fusion proteins were accumulated specifically in the tonoplast membranes and were localized predominantly in the pericycle and xylem parenchyma cells of roots and hypocotyls. In roots, SULTR4;1 was constantly accumulated regardless of the changes of sulfur conditions, whereas SULTR4;2 became abundant by sulfur limitation. In shoots, both transporters were accumulated by sulfur limitation. Vacuoles isolated from callus of the sultr4;1 sultr4;2 double knockout showed excess accumulation of sulfate, which was substantially decreased by overexpression of SULTR4;1-GFP. In seedlings, the supplied [(35)S]sulfate was retained in the root tissue of the sultr4;1 sultr4;2 double knockout mutant. Comparison of the double and single knockouts suggested that SULTR4;1 plays a major role and SULTR4;2 has a supplementary function. Overexpression of SULTR4;1-GFP significantly decreased accumulation of [(35)S]sulfate in the root tissue, complementing the phenotype of the double mutant. These results suggested that SULTR4-type transporters, particularly SULTR4;1, actively mediate the efflux of sulfate from the vacuole lumen into the cytoplasm and influence the capacity for vacuolar storage of sulfate in the root tissue. The efflux function will promote rapid turnover of sulfate from the vacuoles particularly in the vasculature under conditions of low-sulfur supply, which will optimize the symplastic (cytoplasmic) flux of sulfate channeled toward the xylem vessels.
تدمد: 1532-298X
1040-4651
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9387d2650236f080d5c99de7b74b3848Test
https://doi.org/10.1105/tpc.104.023960Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....9387d2650236f080d5c99de7b74b3848
قاعدة البيانات: OpenAIRE