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本文引用的文献

1
Measuring intracellular ca levels in plant cells using the fluorescent probes, indo-1 and fura-2 : progress and prospects.使用荧光探针 indo-1 和 fura-2 测量植物细胞内的 ca 水平:进展与展望。
Plant Physiol. 1990 Jul;93(3):841-5. doi: 10.1104/pp.93.3.841.
2
Mode of action of abscisic Acid in barley aleurone layers : abscisic Acid induces its own conversion to phaseic Acid.脱落酸在大麦糊粉层中的作用方式:脱落酸诱导自身向玉米素羧酸的转化。
Plant Physiol. 1984 Aug;75(4):1126-32. doi: 10.1104/pp.75.4.1126.
3
Role of Calcium in Signal Transduction of Commelina Guard Cells.钙在鸭跖草保卫细胞信号转导中的作用。
Plant Cell. 1991 Apr;3(4):333-344. doi: 10.1105/tpc.3.4.333.
4
Evidence for an Extracellular Reception Site for Abscisic Acid in Commelina Guard Cells.鸭跖草保卫细胞中脱落酸细胞外受体位点的证据。
Plant Physiol. 1994 Apr;104(4):1177-1183. doi: 10.1104/pp.104.4.1177.
5
Visualizing Enzyme Secretion from Individual Barley (Hordeum vulgare) Aleurone Protoplasts.可视化单个大麦(Hordeum vulgare)糊粉层原生质体的酶分泌
Plant Physiol. 1993 May;102(1):279-286. doi: 10.1104/pp.102.1.279.
6
An auxin-binding protein is localized to the plasma membrane of maize coleoptile cells: identification by photoaffinity labeling and purification of a 23-kda polypeptide.一种生长素结合蛋白定位于玉米胚芽鞘细胞的质膜:通过光亲和标记鉴定并纯化出一种23 kDa的多肽。
Proc Natl Acad Sci U S A. 1992 Jan 15;89(2):475-9. doi: 10.1073/pnas.89.2.475.
7
Characterization of a G-protein-regulated outward K+ current in mesophyll cells of vicia faba L.蚕豆叶肉细胞中G蛋白调节的外向钾离子电流的特性分析
Proc Natl Acad Sci U S A. 1993 Jan 1;90(1):262-6. doi: 10.1073/pnas.90.1.262.
8
Gibberellic acid and abscisic acid coordinately regulate cytoplasmic calcium and secretory activity in barley aleurone protoplasts.赤霉素和脱落酸协同调节大麦糊粉层原生质体中的细胞质钙和分泌活性。
Proc Natl Acad Sci U S A. 1992 Apr 15;89(8):3591-5. doi: 10.1073/pnas.89.8.3591.
9
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.
10
Gibberellin perception and the Avena fatua aleurone: do our molecular keys fit the correct locks?赤霉素感知与野燕麦糊粉层:我们的分子钥匙能打开正确的锁吗?
Biochem Soc Trans. 1992 Feb;20(1):85-9. doi: 10.1042/bst0200085.

大麦(Hordeum vulgare L.)糊粉层原生质体质膜外表面对赤霉素和脱落酸的感知

Perception of Gibberellin and Abscisic Acid at the External Face of the Plasma Membrane of Barley (Hordeum vulgare L.) Aleurone Protoplasts.

作者信息

Gilroy S., Jones R. L.

机构信息

Department of Plant Biology, University of California, 111 Koshland Hall, Berkeley, California 94720.

出版信息

Plant Physiol. 1994 Apr;104(4):1185-1192. doi: 10.1104/pp.104.4.1185.

DOI:10.1104/pp.104.4.1185
PMID:12232156
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC159279/
Abstract

The response of protoplasts isolated from aleurone layers of barley (Hordeum vulgare L. cv Himalaya) to internally and externally applied hormone was analyzed to localize the site of perception of the hormonal signal. Protoplasts responded to externally applied gibberellic acid (GA3) with increased synthesis and secretion of [alpha]-amylase, transient expression of the glucuronidase reporter gene fused to the hormone-responsive elements of the [alpha]-amylase promoter, and the vacuolation typical of GA3-treated aleurone cells. When up to 250 [mu]M GA3 was microinjected into the protoplast cytoplasm, none of these responses were observed. This did not reflect damage to the protoplasts during the microinjection procedure, since microinjected protoplasts remained responsive to externally applied hormone. Nor did it reflect loss of microinjected GA3 from the protoplast, since 50% of microinjected [3H]GA20 was retained by protoplasts for at least 24 h. Externally applied abscisic acid (ABA) could reverse the stimulation of [alpha]-amylase synthesis and secretion, whereas microinjecting up to 250 [mu]M ABA was ineffective at antagonizing the stimulatory effect of GA3. These results suggest that the site of perception of GA3 and ABA in the barley aleurone protoplast is on the external face of the plasma membrane.

摘要

分析从大麦(Hordeum vulgare L. cv Himalaya)糊粉层分离的原生质体对内部和外部施加激素的反应,以确定激素信号的感知位点。原生质体对外源施加的赤霉素(GA3)作出反应,表现为α-淀粉酶的合成和分泌增加、与α-淀粉酶启动子的激素反应元件融合的葡糖醛酸酶报告基因的瞬时表达,以及GA3处理的糊粉层细胞典型的液泡化。当向原生质体细胞质中显微注射高达250μM的GA3时,未观察到这些反应。这并不反映显微注射过程中原生质体受到损伤,因为显微注射的原生质体对外源施加的激素仍有反应。这也不反映显微注射的GA3从原生质体中流失,因为50%显微注射的[3H]GA20至少在原生质体中保留24小时。外源施加脱落酸(ABA)可逆转对α-淀粉酶合成和分泌的刺激,而显微注射高达250μM的ABA在拮抗GA3的刺激作用方面无效。这些结果表明,大麦糊粉层原生质体中GA3和ABA的感知位点位于质膜的外表面。