Rice SPX1 and SPX2 inhibit phosphate starvation responses through interacting with PHR2 in a phosphate-dependent manner
about
Engineering food crops to grow in harsh environmentsSPX proteins regulate Pi homeostasis and signaling in different subcellular levelReplace, reuse, recycle: improving the sustainable use of phosphorus by plantsControl of eukaryotic phosphate homeostasis by inositol polyphosphate sensor domainsDissecting nutrient-related co-expression networks in phosphate starved poplarsA novel role for the root cap in phosphate uptake and homeostasis.Identification and expression analysis of OsLPR family revealed the potential roles of OsLPR3 and 5 in maintaining phosphate homeostasis in riceGenome-Wide Identification and Analysis of Genes, Conserved between japonica and indica Rice Cultivars, that Respond to Low-Temperature Stress at the Vegetative Growth Stage.SPX1 is a phosphate-dependent inhibitor of Phosphate Starvation Response 1 in Arabidopsis.Integration of P, S, Fe, and Zn nutrition signals in Arabidopsis thaliana: potential involvement of PHOSPHATE STARVATION RESPONSE 1 (PHR1).Stress induced gene expression drives transient DNA methylation changes at adjacent repetitive elements.Identification of plant vacuolar transporters mediating phosphate storageDeciphering Phosphate Deficiency-Mediated Temporal Effects on Different Root Traits in Rice Grown in a Modified Hydroponic SystemHeat Stress Affects Pi-related Genes Expression and Inorganic Phosphate Deposition/Accumulation in BarleyInteraction between carbon metabolism and phosphate accumulation is revealed by a mutation of a cellulose synthase-like protein, CSLF6.Tissue specific transcript profiling of wheat phosphate transporter genes and its association with phosphate allocation in grains.Genome-Wide Identification and Characterization of SPX Domain-Containing Members and Their Responses to Phosphate Deficiency in Brassica napus.Integrative Comparison of the Role of the PHOSPHATE RESPONSE1 Subfamily in Phosphate Signaling and Homeostasis in Rice.NPKS uptake, sensing, and signaling and miRNAs in plant nutrient stress.Performance and Limitations of Phosphate Quantification: Guidelines for Plant Biologists.Role of vacuoles in phosphorus storage and remobilization.Improving phosphorus use efficiency: a complex trait with emerging opportunities.Transport and homeostasis of potassium and phosphate: limiting factors for sustainable crop production.AtSPX1 affects the AtPHR1 -DNA binding equilibrium by binding monomeric AtPHR1 in solution.Arabidopsis PHL2 and PHR1 Act Redundantly as the Key Components of the Central Regulatory System Controlling Transcriptional Responses to Phosphate Starvation.Rice SPX-Major Facility Superfamily3, a Vacuolar Phosphate Efflux Transporter, Is Involved in Maintaining Phosphate Homeostasis in Rice.Down-regulation of OsSPX1 caused semi-male sterility, resulting in reduction of grain yield in riceStMYB44 negatively regulates phosphate transport by suppressing expression of PHOSPHATE1 in potato.The rice CK2 kinase regulates trafficking of phosphate transporters in response to phosphate levels.Altered Expression of OsNLA1 Modulates Pi Accumulation in Rice (Oryza sativa L.) Plants.GmPHR25, a GmPHR member up-regulated by phosphate starvation, controls phosphate homeostasis in soybean.Evolution of the SPX gene family in plants and its role in the response mechanism to phosphorus stress.The EXS Domain of PHO1 Participates in the Response of Shoots to Phosphate Deficiency via a Root-to-Shoot Signal.The phosphate transporters LjPT4 and MtPT4 mediate early root responses to phosphate status in non mycorrhizal roots.Rice nucleosome patterns undergo remodeling coincident with stress-induced gene expression.GIPS: A Software Guide to Sequencing-Based Direct Gene Cloning in Forward Genetics Studies.The role of OsPT8 in arsenate uptake and varietal difference in arsenate tolerance in rice.Understanding Fe2+ toxicity and P deficiency tolerance in rice for enhancing productivity under acidic soils.The Chloroplast Protease AMOS1/EGY1 Affects Phosphate Homeostasis under Phosphate Stress.Characterization of the AtSPX3 Promoter Elucidates its Complex Regulation in Response to Phosphorus Deficiency.
P2860
Q26784195-589388A3-88C0-4643-8A9E-A5C27837D457Q26801707-73217CA6-4EEB-47C2-85A5-87309CB05D96Q26859282-2F69D487-56D9-44A3-8CD2-914D0595D85AQ27704571-44B70E72-4725-4D1A-82D8-5494A63FAA1DQ30378484-7142CE9E-51B4-4FC6-8D6E-DD4C17D6052FQ33362905-041F1CA2-F42B-48A6-AC40-5F1EBF7E5FFAQ33364038-90EEABAF-F32F-4301-820A-3D76706C1E4DQ33855308-D11C7AAC-FE68-4102-9E14-41730CC90FE6Q34383930-6A9B5C83-4F09-4D21-9AF1-087C827B34D0Q35545436-DAD73253-10AC-4387-89F6-D99B98BED9ACQ35947977-A66A94CD-2B78-4D1C-9082-13B2DCA11B00Q36768265-32FF936D-A1AA-4C39-BF4D-9D3855A650D2Q36864235-67C1E6DF-8350-485C-A8EE-8BC4D27E7036Q37034143-C81A342E-13A8-4166-980B-C5650F9BD34AQ37179853-BED7B602-B6FA-4C0E-A30D-84957809D9B4Q37519456-1CAB5AEF-AFC5-4C63-958B-869591C0D79AQ37604128-179FB27E-EF61-4D33-A0A8-352E4C9D74C1Q38298240-27ABBC78-9446-4EE0-8AC0-77D32E67F8E8Q38530654-7DF23609-2F22-46A8-87CB-0DC7F00C9215Q38729141-952B42B5-EE89-4EED-B8EC-2B90ECCA8E49Q38771707-63F865B6-FADC-4F84-A051-97C81895808DQ39012380-45F75433-69D1-410A-8FD6-F3FE8777CADFQ39037953-02879AD0-75D0-4D1F-AF19-3CBF1A6E2E88Q40059671-27F32150-78F5-4EF0-9E84-5AD7B1A6CCA5Q40299228-A1BE0CA5-E940-4064-940A-0CAB03D794E7Q40480543-174BE879-ACF1-4520-9E55-B25A4DFB0743Q41477192-3D990724-1ABF-454E-A0A7-80439D4D6AE6Q42063476-7E22A399-A16D-47AD-8220-A894EA5A65A0Q42158822-E3876900-DFA7-4DF3-8D62-BFBF76B8BEDEQ42230389-182EE021-8A9A-4363-ABCC-AB096153975CQ46290672-6FD604A3-37B3-4522-BB96-F043F8DD4209Q47212735-B5E33044-B8A4-4E5C-9D34-F9C4296DF065Q48107707-20696DD8-1561-4ADA-BEA5-F16B8E733E6AQ48118488-0A1F55C6-99BA-436E-8039-BACB9A8BBECCQ48158685-C79D6206-B60B-40B7-B630-B3F56EDA5332Q48247576-761D0B6B-0B5F-4887-B0A2-9C3ACEBE21DDQ48248650-F536D5CD-70B7-496B-9F71-44EAC68C2095Q50016455-7AAF0886-103C-4763-8513-AF70ED926E60Q50492846-8CD47547-87BF-4E41-8B04-3E7BC348F42BQ50500539-1135C98B-66BB-4851-AC4B-D2BA2ECC2701
P2860
Rice SPX1 and SPX2 inhibit phosphate starvation responses through interacting with PHR2 in a phosphate-dependent manner
description
2014 nî lūn-bûn
@nan
2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Rice SPX1 and SPX2 inhibit pho ...... n a phosphate-dependent manner
@ast
Rice SPX1 and SPX2 inhibit pho ...... n a phosphate-dependent manner
@en
Rice SPX1 and SPX2 inhibit pho ...... n a phosphate-dependent manner
@nl
type
label
Rice SPX1 and SPX2 inhibit pho ...... n a phosphate-dependent manner
@ast
Rice SPX1 and SPX2 inhibit pho ...... n a phosphate-dependent manner
@en
Rice SPX1 and SPX2 inhibit pho ...... n a phosphate-dependent manner
@nl
prefLabel
Rice SPX1 and SPX2 inhibit pho ...... n a phosphate-dependent manner
@ast
Rice SPX1 and SPX2 inhibit pho ...... n a phosphate-dependent manner
@en
Rice SPX1 and SPX2 inhibit pho ...... n a phosphate-dependent manner
@nl
P2093
P2860
P356
P1476
Rice SPX1 and SPX2 inhibit pho ...... n a phosphate-dependent manner
@en
P2093
Changying Li
Chuanzao Mao
Huixia Shou
Wenyuan Ruan
Xiaorong Mo
P2860
P304
14953-14958
P356
10.1073/PNAS.1404680111
P407
P577
2014-09-30T00:00:00Z