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rolB转化烟草原生质体中生长素感知的变化。rolB mRNA表达的时间进程和生长素敏感性的增加揭示了生长素的多重调控。

Alterations of auxin perception in rolB-transformed tobacco protoplasts. Time course of rolB mRNA expression and increase in auxin sensitivity reveal multiple control by auxin.

作者信息

Maurel C, Leblanc N, Barbier-Brygoo H, Perrot-Rechenmann C, Bouvier-Durand M, Guern J

机构信息

Institut des Sciences Végétales, Centre National de la Recherche Scientifique, Gif-sur-Yvette, France.

出版信息

Plant Physiol. 1994 Aug;105(4):1209-15. doi: 10.1104/pp.105.4.1209.

DOI:10.1104/pp.105.4.1209
PMID:7972494
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC159450/
Abstract

Expression and physiological effects of the root-inducing rolB gene of Agrobacterium rhizogenes T-DNA were studied simultaneously in tobacco (Nicotiana tabacum) mesophyll protoplasts. The kinetic study of the expression of rolB mRNA following exogenous auxin application showed that auxin transiently stimulated rolB expression, with mRNA levels starting to accumulate 6 to 9 h after auxin was supplied and increasing 300-fold after 12 to 18 h. The parallel study of the auxin sensitivity of rolB-transformed protoplasts, as assayed by their electrical response to the hormone, showed that the auxin treatment generated an increase in sensitivity by a factor of up to 100,000, whereas in untransformed protoplasts the same auxin treatment induced an increase in auxin sensitivity that never exceeded 30- to 50-fold. This reflects a strong cooperative effect of auxin and rolB in transformed protoplasts. Surprisingly, the maximal increase in sensitivity was observed several hours before the maximal accumulation of rolB mRNA, suggesting that the dramatic control of auxin sensitivity by auxin in rolB-transformed protoplasts requires only low levels of rolB expression. Antibodies directed against ZmER-abp1, the major auxin-binding protein from maize, differentially altered the auxin sensitivity of the electrical response of rolB-transformed and normal protoplasts. This suggests that alterations of the auxin reception-transduction pathway at the plasma membrane of rolB-transformed protoplasts may account for their increased auxin sensitivity.

摘要

发根农杆菌T-DNA的诱导根rolB基因在烟草(Nicotiana tabacum)叶肉原生质体中的表达及生理效应被同时进行了研究。对外源生长素处理后rolB mRNA表达的动力学研究表明,生长素短暂刺激rolB表达,在供应生长素后6至9小时mRNA水平开始积累,12至18小时后增加300倍。通过对rolB转化原生质体对激素的电反应测定来平行研究其生长素敏感性,结果显示生长素处理使敏感性提高了高达100,000倍,而在未转化的原生质体中,相同的生长素处理诱导的生长素敏感性增加从未超过30至50倍。这反映了生长素和rolB在转化原生质体中有很强的协同效应。令人惊讶的是,在rolB mRNA最大积累之前数小时就观察到了敏感性的最大增加,这表明在rolB转化的原生质体中,生长素对生长素敏感性的显著调控仅需要低水平的rolB表达。针对玉米主要生长素结合蛋白ZmER-abp1的抗体,对rolB转化原生质体和正常原生质体电反应的生长素敏感性产生了不同的影响。这表明rolB转化原生质体质膜上生长素接收-转导途径的改变可能是其生长素敏感性增加的原因。

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1
Alterations of auxin perception in rolB-transformed tobacco protoplasts. Time course of rolB mRNA expression and increase in auxin sensitivity reveal multiple control by auxin.rolB转化烟草原生质体中生长素感知的变化。rolB mRNA表达的时间进程和生长素敏感性的增加揭示了生长素的多重调控。
Plant Physiol. 1994 Aug;105(4):1209-15. doi: 10.1104/pp.105.4.1209.
2
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本文引用的文献

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High Sensitivity to Auxin is a Common Feature of Hairy Root.生长素高敏感性是毛状根的共同特征。
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Auxin effect on the transmembrane potential difference of wild-type and mutant tobacco protoplasts exhibiting a differential sensitiity to auxin.生长素对表现出对生长素不同敏感性的野生型和突变型烟草原生质体跨膜电位差的影响。
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The rolB Gene of Agrobacterium rhizogenes Does Not Increase the Auxin Sensitivity of Tobacco Protoplasts by Modifying the Intracellular Auxin Concentration.发根农杆菌的rolB基因不会通过改变细胞内生长素浓度来提高烟草原生质体对生长素的敏感性。
Plant Physiol. 1994 Jun;105(2):563-569. doi: 10.1104/pp.105.2.563.
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Expression of Agrobacterium rhizogenes rolB gene fusions in Escherichia coli: production of antibodies against the RolB protein.发根农杆菌rolB基因融合体在大肠杆菌中的表达:抗RolB蛋白抗体的产生
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Different promoter regions control level and tissue specificity of expression of Agrobacterium rhizogenes rolB gene in plants.不同的启动子区域控制发根农杆菌rolB基因在植物中的表达水平和组织特异性。
Plant Mol Biol. 1991 Mar;16(3):427-36. doi: 10.1007/BF00023993.
10
Antibodies to a peptide from the maize auxin-binding protein have auxin agonist activity.针对玉米生长素结合蛋白中一段肽的抗体具有生长素激动剂活性。
Proc Natl Acad Sci U S A. 1992 Aug 1;89(15):7208-12. doi: 10.1073/pnas.89.15.7208.