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本文引用的文献

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Nuclear targeting in plants.植物中的核靶向。
Plant Physiol. 1992 Dec;100(4):1627-32. doi: 10.1104/pp.100.4.1627.
2
GIBBERELLIN BIOSYNTHESIS: Enzymes, Genes and Their Regulation.赤霉素生物合成:酶、基因及其调控
Annu Rev Plant Physiol Plant Mol Biol. 1997 Jun;48:431-460. doi: 10.1146/annurev.arplant.48.1.431.
3
Cloning the Arabidopsis GA1 Locus by Genomic Subtraction.通过基因组消减克隆拟南芥GA1基因座
Plant Cell. 1992 Feb;4(2):119-128. doi: 10.1105/tpc.4.2.119.
4
Derivative Alleles of the Arabidopsis Gibberellin-Insensitive (gai) Mutation Confer a Wild-Type Phenotype.拟南芥赤霉素不敏感(gai)突变的衍生等位基因赋予野生型表型。
Plant Cell. 1993 Mar;5(3):351-360. doi: 10.1105/tpc.5.3.351.
5
Perception of Gibberellin and Abscisic Acid at the External Face of the Plasma Membrane of Barley (Hordeum vulgare L.) Aleurone Protoplasts.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
Plant Physiol. 1994 Apr;104(4):1185-1192. doi: 10.1104/pp.104.4.1185.
6
Phenotypic Suppression of the Gibberellin-Insensitive Mutant (gai) of Arabidopsis.拟南芥赤霉素不敏感突变体(gai)的表型抑制
Plant Physiol. 1995 Jun;108(2):495-502. doi: 10.1104/pp.108.2.495.
7
Genetic Analysis of Gibberellin Signal Transduction.赤霉素信号转导的遗传分析
Plant Physiol. 1996 Sep;112(1):11-17. doi: 10.1104/pp.112.1.11.
8
The Arabidopsis GAI gene defines a signaling pathway that negatively regulates gibberellin responses.拟南芥GAI基因定义了一条对赤霉素反应起负调控作用的信号通路。
Genes Dev. 1997 Dec 1;11(23):3194-205. doi: 10.1101/gad.11.23.3194.
9
Developmental regulation of the gibberellin biosynthetic gene GA1 in Arabidopsis thaliana.拟南芥中赤霉素生物合成基因GA1的发育调控
Plant J. 1997 Jul;12(1):9-19. doi: 10.1046/j.1365-313x.1997.12010009.x.
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Sequence and characterization of two Arabidopsis thaliana cDNAs isolated by functional complementation of a yeast gln3 gdh1 mutant.
FEBS Lett. 1997 Jun 30;410(2-3):213-8. doi: 10.1016/s0014-5793(97)00590-5.

拟南芥RGA基因编码一种转录调节因子,可抑制赤霉素信号转导途径。

The Arabidopsis RGA gene encodes a transcriptional regulator repressing the gibberellin signal transduction pathway.

作者信息

Silverstone A L, Ciampaglio C N, Sun T

机构信息

Developmental, Cell and Molecular Biology Group, Department of Botany, Box 91000, Duke University, Durham, North Carolina 27708-1000, USA.

出版信息

Plant Cell. 1998 Feb;10(2):155-69. doi: 10.1105/tpc.10.2.155.

DOI:10.1105/tpc.10.2.155
PMID:9490740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC143987/
Abstract

The recessive rga mutation is able to partially suppress phenotypic defects of the Arabidopsis gibberellin (GA) biosynthetic mutant ga1-3. Defects in stem elongation, flowering time, and leaf abaxial trichome initiation are suppressed by rga. This indicates that RGA is a negative regulator of the GA signal transduction pathway. We have identified 10 additional alleles of rga from a fast-neutron mutagenized ga1-3 population and used them to isolate the RGA gene by genomic subtraction. Our data suggest that RGA may be functioning as a transcriptional regulator. RGA was found to be a member of the VHIID regulatory family, which includes the radial root organizing gene SCARECROW and another GA signal transduction repressor, GAI. RGA and GAI proteins share a high degree of homology, but their N termini are more divergent. The presence of several structural features, including homopolymeric serine and threonine residues, a putative nuclear localization signal, leucine heptad repeats, and an LXXLL motif, indicates that the RGA protein may be a transcriptional regulator that represses the GA response. In support of the putative nuclear localization signal, we demonstrated that a transiently expressed green fluorescent protein-RGA fusion protein is localized to the nucleus in onion epidermal cells. Because the rga mutation abolished the high level of expression of the GA biosynthetic gene GA4 in the ga1-3 mutant background, we conclude that RGA may also play a role in controlling GA biosynthesis.

摘要

隐性rga突变能够部分抑制拟南芥赤霉素(GA)生物合成突变体ga1-3的表型缺陷。rga抑制了茎伸长、开花时间和叶片下表皮毛起始方面的缺陷。这表明RGA是GA信号转导途径的负调控因子。我们从经快中子诱变的ga1-3群体中鉴定出了10个额外的rga等位基因,并利用它们通过基因组扣除法分离出了RGA基因。我们的数据表明RGA可能作为转录调节因子发挥作用。发现RGA是VHIID调节家族的成员,该家族包括径向根组织基因SCARECROW和另一个GA信号转导抑制因子GAI。RGA和GAI蛋白具有高度同源性,但它们的N端差异更大。包括同聚丝氨酸和苏氨酸残基、一个假定的核定位信号、亮氨酸七聚体重复序列和一个LXXLL基序在内的几个结构特征的存在,表明RGA蛋白可能是一个抑制GA反应的转录调节因子。为了支持假定的核定位信号,我们证明了瞬时表达的绿色荧光蛋白-RGA融合蛋白在洋葱表皮细胞中定位于细胞核。由于rga突变消除了ga1-3突变背景下GA生物合成基因GA4的高水平表达,我们得出结论,RGA可能在控制GA生物合成中也发挥作用。