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Aquaporin OsPIP2;2 Regulates Bakanae Disease Resistance in Rice
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作者 LIU Xin LI Chanyuan +2 位作者 CHEN Ling OUYANG Younan JI Zhijuan 《Rice science》 2025年第4期457-461,I0023-I0027,共10页
Bakanae disease,induced by the pathogen Fusarium fujikuroi,poses a significant stress on rice cultivation.However,the key resistance genes to this disease remain largely unknown.In this study,we reported that the plas... Bakanae disease,induced by the pathogen Fusarium fujikuroi,poses a significant stress on rice cultivation.However,the key resistance genes to this disease remain largely unknown.In this study,we reported that the plasma membrane intrinsic protein,OsPIP2;2,positively regulated to bakanae disease resistance in rice. 展开更多
关键词 bakanae disease ospip plasma membrane intrinsic proteinospip positively Fusarium fujikuroi resistance genes AQUAPORIN Bakanae disease bakanae diseaseinduced
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水稻OsPIP1;2植物过表达及亚细胞定位载体的构建 被引量:1
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作者 魏毅东 张扬 +3 位作者 许惠滨 谢华安 王宗华 张建福 《分子植物育种》 CAS CSCD 北大核心 2013年第4期485-493,共9页
水稻质膜内在蛋白OsPIPs是细胞水分运输的关键蛋白,与多种重要物质的运输交换有关,并在生长发育的各个阶段发挥重要作用。为了挖掘水稻OsPIP1;2基因的功能和应用,本研究利用电子克隆从提取的水稻叶片RNA中成功克隆了OsPIP1;2CDS序列,将... 水稻质膜内在蛋白OsPIPs是细胞水分运输的关键蛋白,与多种重要物质的运输交换有关,并在生长发育的各个阶段发挥重要作用。为了挖掘水稻OsPIP1;2基因的功能和应用,本研究利用电子克隆从提取的水稻叶片RNA中成功克隆了OsPIP1;2CDS序列,将其连接到植物表达载体pCAMBIA1301上,构建了35S启动子驱动的OsPIP1;2过表达载体,并成功将其导入到农杆菌EHA105中。此外,为了更全面的了解OsPIP1;2蛋白的亚细胞定位情况,本研究将不同的荧光蛋白分别融合到OsPIP1;2的N端和C端,构建了两个亚细胞定位载体。以上载体的构建,为深入了解和研究OsPIP1;2在水稻中的功能打下了基础。 展开更多
关键词 水稻质膜内在蛋白 ospip12 亚细胞定位 载体构建
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水稻水通道蛋白OsPIP1;3与白叶枯病菌harpin蛋白Hpa1互作关系研究 被引量:2
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作者 王欢 田沂民 董汉松 《植物生理学报》 CAS CSCD 北大核心 2016年第8期1223-1230,共8页
本文通过片段缺失和定点突变的方法构建产生水稻(Oryza sativa)水通道蛋白OsPIP1;3的变异本。通过膜酵母双杂交进行蛋白互作分析,实验结果表明水稻白叶枯病菌(Xanthomonas oryzae pv.oryzae)harpin蛋白Hpa1能与OsPIP1;3互作,但如果... 本文通过片段缺失和定点突变的方法构建产生水稻(Oryza sativa)水通道蛋白OsPIP1;3的变异本。通过膜酵母双杂交进行蛋白互作分析,实验结果表明水稻白叶枯病菌(Xanthomonas oryzae pv.oryzae)harpin蛋白Hpa1能与OsPIP1;3互作,但如果将OsPIP1;3的一个胞外序列(loopE)及OsPIP1;3的第六个跨膜区域(TM6)删除,则互作不能发生。进一步对276-279 aa进行替换,OsPIP1;3与Hpa1不再发生互作。这些结果说明,OsPIP1;3序列上的loop E和TM6上的氨基酸对OsPIP1;3–Hpa1互作有重要影响,而276-279 aa是可能的互作位点。 展开更多
关键词 Hpa1 ospip1 3 定点突变 膜酵母双杂交 蛋白互作
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A cluster of mutagenesis revealed an osmotic regulatory role of the OsPIP1 genes in enhancing rice salt tolerance 被引量:2
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作者 Leyuan Tao Bing Wang +6 位作者 Shichao Xin Wei Li Shengcai Huang Laihua Liu Jing Cui Qianru Zhang Xianguo Cheng 《The Crop Journal》 SCIE CSCD 2023年第4期1204-1217,共14页
Aquaporins play important regulatory roles in improving plant abiotic stress tolerance.To better understand whether the Os PIP1 genes collectively dominate the osmotic regulation in rice under salt stress,a cluster ed... Aquaporins play important regulatory roles in improving plant abiotic stress tolerance.To better understand whether the Os PIP1 genes collectively dominate the osmotic regulation in rice under salt stress,a cluster editing of the Os PIP1;1,Os PIP1;2 and Os PIP1;3 genes in rice was performed by CRISPR/Cas9 system.Sequencing showed that two mutants with Cas9-free,line 14 and line 18 were successfully edited.Briefly,line 14 deleted a single C base in both the Os PIP1;1 and Os PIP1;3 genes,and inserted a single T base in the Os PIP1;2 gene,respectively.While line 18 demonstrated an insertion of a single A base in the Os PIP1;1gene and a single T base in both the Os PIP1;2 and Os PIP1;3 genes,respectively.Multiplex editing of the Os PIP1 genes significantly inhibited photosynthetic rate and accumulation of compatible metabolites,but increased MDA contents and osmotic potentials in the mutants,thus delaying rice growth under salt stress.Functional loss of the Os PIP1 genes obviously suppressed the expressions of the Os PIP1,Os SOS1,Os CIPK24 and Os CBL4 genes,and increased the influxes of Na+and effluxes of K^(+)/H^(+)in the roots,thus accumulating more Na+in rice mutants under salt stress.This study suggests that the Os PIP1 genes are essential modulators collectively contributing to the enhancement of rice salt stress tolerance,and multiplex editing of the Os PIP1 genes provides insight into the osmotic regulation of the PIP genes. 展开更多
关键词 AQUAPORIN Multiplex gene editing CRISPR/Cas9 ospip1 genes Rice(Oryza sativa L.) Salt tolerance
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Differential Responses of Water Uptake Pathways and Expression of Two Aquaporin Genes to Water-Deficit in Rice Seedlings of Two Genotypes
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作者 XUAi-hua CUIKe-hui +5 位作者 WANGWen-cheng WANGZhen-mei HUANG Jian-liang NIE Li-xiao LI Yong PENG Shao-bing 《Rice science》 SCIE CSCD 2017年第4期187-197,共11页
Water-deficit (WD) is a major abiotic stress constraining crop productivity worldwide. Zhenshan 97 is a drought-susceptible rice genotype, while IRAT109 is a drought-resistant one. However, the physiological basis o... Water-deficit (WD) is a major abiotic stress constraining crop productivity worldwide. Zhenshan 97 is a drought-susceptible rice genotype, while IRAT109 is a drought-resistant one. However, the physiological basis of the difference remains unclear. These two genotypes had similar total water uptake rates under both WD and well-watered (WW) conditions, and their water uptake rates under WD were significantly decreased compared with those under WW. However, the water uptake rate via the cell-to-cell pathway was significantly increased in Zhenshan 97 but decreased in IRAT109 under WD, whereas the opposite trends were observed through the apoplastic pathway. These results indicated that the stress responses and relative contributions of these two water uptake pathways were associated with rice genotype under WD. The expression levels of OsPIP2;4 and OsPIP2;5 genes were significantly higher in roots of Zhenshan 97 than in IRAT109 under the two conditions. OsPIP2;4 expression in roots was significantly up-regulated under WD, while OsPIP2;5 expression showed no significant change. These results suggest that the expression levels of OsPIP2;4 and OsPIP2;5 in rice are dependent on genotype and water availability. Compared with Zhenshan 97, IRAT109 had a higher root dry weight, water uptake rate and xylem sap flow rate, and lower leaf water potential and root porosity under WD, which might be responsible for the drought resistance in IRAT109. 展开更多
关键词 aquaporin expression ospip2 4 ospip2 5 rice root porosity WATER-DEFICIT water uptake pathway
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