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Agrobacterium tumefaciens-mediated transformation of Arabidopsis thaliana root explants by using kanamycin selection.利用卡那霉素筛选进行拟南芥根外植体的根癌农杆菌介导转化。
Proc Natl Acad Sci U S A. 1988 Aug;85(15):5536-40. doi: 10.1073/pnas.85.15.5536.
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14-3-3 PROTEINS AND SIGNAL TRANSDUCTION.14-3-3蛋白与信号转导
Annu Rev Plant Physiol Plant Mol Biol. 1996 Jun;47:49-73. doi: 10.1146/annurev.arplant.47.1.49.
3
Ablation of Papillar Cell Function in Brassica Flowers Results in the Loss of Stigma Receptivity to Pollination.甘蓝型油菜花朵中乳头细胞功能的消融导致柱头对授粉的接受性丧失。
Plant Cell. 1993 Mar;5(3):263-275. doi: 10.1105/tpc.5.3.263.
4
Identification of genes required for pollen-stigma recognition in Arabidopsis thaliana.拟南芥花粉-柱头识别所需基因的鉴定。
Plant J. 1995 Nov;8(5):703-14. doi: 10.1046/j.1365-313x.1995.08050703.x.
5
A conditional sterile mutation eliminates surface components from Arabidopsis pollen and disrupts cell signaling during fertilization.一种条件性不育突变会消除拟南芥花粉的表面成分,并在受精过程中破坏细胞信号传导。
Genes Dev. 1993 Jun;7(6):974-85. doi: 10.1101/gad.7.6.974.
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Phosphorylation and calcium binding properties of an Arabidopsis GF14 brain protein homolog.拟南芥GF14脑蛋白同源物的磷酸化和钙结合特性
Plant Cell. 1994 Apr;6(4):501-10. doi: 10.1105/tpc.6.4.501.
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Mapping of transcriptional start and capping points by a modified 5' RACE technique.采用改良的5' RACE技术对转录起始点和加帽位点进行定位。
Biotechniques. 1994 May;16(5):807-8.
8
A single Arabidopsis GF14 isoform possesses biochemical characteristics of diverse 14-3-3 homologues.单个拟南芥GF14亚型具有多种14-3-3同源物的生化特性。
Plant Mol Biol. 1994 Jul;25(4):659-67. doi: 10.1007/BF00029604.
9
Characterization of 14-3-3 proteins in adrenal chromaffin cells and demonstration of isoform-specific phospholipid binding.肾上腺嗜铬细胞中14-3-3蛋白的特性及亚型特异性磷脂结合的证明。
Biochem J. 1994 Jul 1;301 ( Pt 1)(Pt 1):305-10. doi: 10.1042/bj3010305.
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Cloning and characterization of the epsilon and zeta isoforms of the 14-3-3 proteins.
DNA Cell Biol. 1994 Jun;13(6):629-40. doi: 10.1089/dna.1994.13.629.

拟南芥14-3-3基因的分子结构与组织特异性表达

Molecular organization and tissue-specific expression of an Arabidopsis 14-3-3 gene.

作者信息

Daugherty C J, Rooney M F, Miller P W, Ferl R J

机构信息

Horticultural Sciences Department, University of Florida, Gainesville 32611, USA.

出版信息

Plant Cell. 1996 Aug;8(8):1239-48. doi: 10.1105/tpc.8.8.1239.

DOI:10.1105/tpc.8.8.1239
PMID:8776894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC161235/
Abstract

The 14-3-3 proteins, originally described as mammalian brain proteins, are ubiquitous in eukaryotes. We isolated an Arabidopsis 14-3-3 gene, designated GRF1-GF14 chi (for general regulatory factor1-G-box factor 14-3-3 homolog isoform chi), and characterized its expression within plant tissues. Sequence comparison of the GRF1-GF14 chi genomic clone with other 14-3-3 proteins demonstrated that the extreme conservation of 14-3-3 residues in several domains is encoded by the first three exons. The highly variable C-terminal domain is encoded by a divergent fourth exon that is unique among 14-3-3 homologs, suggesting that exon shuffling might confer gene-specific functions among the isoforms. The anatomical distribution and developmental expression of the Arabidopsis 14-3-3 protein were examined in transgenic plants carrying a GRF1-GF14 chi promoter-beta-glucuronidase construct. GF14 chi promoter activity was observed in the roots of both seedlings and mature plants. In immature flowers, GF14 chi promoter activity was localized to the buds. However, as the flowers matured, GF14 chi promoter activity was restricted to the stigma, anthers, and pollen. In immature siliques, GF14 chi promoter activity was initially localized to styles and abscission zones but was subsequently observed throughout mature siliques. In situ hybridization demonstrated that GF14 chi mRNA expression was prominent in epidermal tissue of roots, petals, and sepals of flower buds, papillae cells of flowers, siliques, and endosperm of immature seeds. Thus, plant 14-3-3 gene expression exhibits cell- and tissue-specific localization rivaling that observed for 14-3-3 proteins within the mammalian brain.

摘要

14-3-3蛋白最初被描述为哺乳动物脑蛋白,在真核生物中普遍存在。我们分离出一个拟南芥14-3-3基因,命名为GRF1-GF14 chi(通用调控因子1-G盒因子14-3-3同源异构体chi),并对其在植物组织中的表达进行了表征。GRF1-GF14 chi基因组克隆与其他14-3-3蛋白的序列比较表明,几个结构域中14-3-3残基的高度保守性由前三个外显子编码。高度可变的C末端结构域由一个不同的第四外显子编码,该外显子在14-3-3同源物中是独特的,这表明外显子重排可能赋予异构体基因特异性功能。在携带GRF1-GF14 chi启动子- β-葡萄糖醛酸酶构建体的转基因植物中检测了拟南芥14-3-3蛋白的解剖分布和发育表达。在幼苗和成熟植物的根中均观察到GF14 chi启动子活性。在未成熟花中,GF14 chi启动子活性定位于芽。然而,随着花的成熟,GF14 chi启动子活性局限于柱头、花药和花粉。在未成熟角果中,GF14 chi启动子活性最初定位于花柱和脱落区,但随后在整个成熟角果中都能观察到。原位杂交表明,GF14 chi mRNA表达在根、花瓣和花芽萼片的表皮组织、花的乳头细胞、角果和未成熟种子的胚乳中很突出。因此,植物14-3-3基因表达表现出细胞和组织特异性定位,可与哺乳动物脑中14-3-3蛋白的定位相媲美。