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GTPase ROP6 negatively modulates phosphate deficiency through inhibition of PHT1;1 and PHT1;4 in Arabidopsis thaliana 被引量:1
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作者 Huiling Gao Tian Wang +5 位作者 Yanting Zhang Lili Li Chuanqing Wang Shiyuan Guo Tianqi Zhang Cun Wang 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2021年第10期1775-1786,共12页
Phosphorus,an essential macroelement for plant growth and development,is a major limiting factor for sustainable crop yield.The Rho of plant(ROP)GTPase is involved in regulating multiple signal transduction processes ... Phosphorus,an essential macroelement for plant growth and development,is a major limiting factor for sustainable crop yield.The Rho of plant(ROP)GTPase is involved in regulating multiple signal transduction processes in plants,but potentially including the phosphate deficiency signaling pathway remains unknown.Here,we identified that the rop6 mutant exhibited a dramatic tolerant phenotype under Pi-deficient conditions,with higher phosphate accumulation and lower anthocyanin content.In contrast,the rop6 mutant was more sensitive to arsenate(As(V))toxicity,the analog of Pi.Immunoblot analysis displayed that the ROP6 protein was rapidly degraded through ubiquitin/26S proteasome pathway under Pi-deficient conditions.In addition,pull-down assay using GST-RIC1 demonstrated that the ROP6 activity was decreased obviously under Pi-deficient conditions.Strikingly,protein-protein interaction and two-voltage clamping assays demonstrated that ROP6 physically interacted with and inhibited the key phosphate uptake transporters PHT1;1 and PHT1;4 in vitro and in vivo.Moreover,genetic analysis showed that ROP6 functioned upstream of PHT1;1 and PHT1;4.Thus,we conclude that GTPase ROP6 modulates the uptake of phosphate by inhibiting the activities of PHT1;1 and PHT1;4 in Arabidopsis. 展开更多
关键词 ARABIDOPSIS AS(V) phosphate deficiency PHT1 1 PHT1 4 rop6
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百脉根结瘤因子受体NFR5及其相互作用蛋白的研究 被引量:1
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作者 陈春芬 朱辉 +2 位作者 杨绮 朱浩 张忠明 《中国油料作物学报》 CAS CSCD 北大核心 2007年第4期372-376,共5页
以豆科植物百脉根的mRNA为模板,利用RT-PCR方法,扩增到1.0kb结瘤因子受体5(nod factorreceptor NFR5)蛋白激酶结构域的DNA片段(nfr5-pk),并将该片段克隆到酵母双杂交BD载体pGBKT7上。通过酵母双杂交技术,筛选接种根瘤菌的百脉根AD-cDNA... 以豆科植物百脉根的mRNA为模板,利用RT-PCR方法,扩增到1.0kb结瘤因子受体5(nod factorreceptor NFR5)蛋白激酶结构域的DNA片段(nfr5-pk),并将该片段克隆到酵母双杂交BD载体pGBKT7上。通过酵母双杂交技术,筛选接种根瘤菌的百脉根AD-cDNA酵母双杂交文库,从文库中分离到与nfr5-pk相互作用的221个阳性克隆。从这些阳性克隆酵母中分离AD质粒经反复验证,对26个确定阳性克隆的外源片段进行测序和同源性分析。通过NCBI数据库比对分析鉴定出小G蛋白Rop6等6个与NFR5-PK相互作用的不同蛋白,为进一步研究NFR5基因的功能和调控机制提供了材料。 展开更多
关键词 酵母双杂交 NFR5 小G蛋白rop6 百脉根
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