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本文引用的文献

1
Coordinate Expression of Rubisco Activase and Rubisco during Barley Leaf Cell Development.大麦叶片细胞发育过程中核酮糖-1,5-二磷酸羧化酶/加氧酶激活酶与核酮糖-1,5-二磷酸羧化酶/加氧酶的协同表达
Plant Physiol. 1989 Jun;90(2):516-21. doi: 10.1104/pp.90.2.516.
2
A Mutant of Arabidopsis thaliana Which Lacks Activation of RuBP Carboxylase In Vivo.拟南芥体内缺乏 RuBP 羧化酶激活突变体。
Plant Physiol. 1982 Aug;70(2):381-7. doi: 10.1104/pp.70.2.381.
3
Multiple DNA-Protein Complexes at a Circadian-Regulated Promoter Element.昼夜节律调控启动子元件处的多个DNA-蛋白质复合物
Plant Cell. 1995 Dec;7(12):2039-2051. doi: 10.1105/tpc.7.12.2039.
4
Differential Involvement of the Circadian Clock in the Expression of Genes Required for Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase Synthesis, Assembly, and Activation in Arabidopsis thaliana.拟南芥生物钟对1,5-二磷酸核酮糖羧化酶/加氧酶合成、组装和激活所需基因表达的差异影响
Plant Physiol. 1993 Oct;103(2):553-564. doi: 10.1104/pp.103.2.553.
5
A DNA binding activity for one of two closely defined phytochrome regulatory elements in an Lhcb promoter is more abundant in etiolated than in green plants.在Lhcb启动子中,两种紧密定义的光敏色素调节元件之一的DNA结合活性在黄化植物中比在绿色植物中更丰富。
Plant Cell. 1996 Jan;8(1):31-41. doi: 10.1105/tpc.8.1.31.
6
CA-1, a novel phosphoprotein, interacts with the promoter of the cab140 gene in Arabidopsis and is undetectable in det1 mutant seedlings.CA-1是一种新型磷蛋白,它与拟南芥中cab140基因的启动子相互作用,并且在det1突变体幼苗中无法检测到。
Plant Cell. 1993 Jan;5(1):109-21. doi: 10.1105/tpc.5.1.109.
7
Investigation of the mechanism underlying the inhibitory effect of heterologous ras genes in plant cells.异源ras基因对植物细胞抑制作用的机制研究。
Plant Mol Biol. 1993 Aug;22(5):751-65. doi: 10.1007/BF00027362.
8
'Circadian clock' directs the expression of plant genes.“生物钟”指导植物基因的表达。
Plant Mol Biol. 1993 Jun;22(3):533-42. doi: 10.1007/BF00015982.
9
Localization of light-inducible and tissue-specific regions of the spinach ribulose bisphosphate carboxylase/oxygenase (rubisco) activase promoter in transgenic tobacco plants.菠菜核酮糖二磷酸羧化酶/加氧酶(rubisco)激活酶启动子在转基因烟草植株中光诱导及组织特异性区域的定位
Plant Mol Biol. 1993 Dec;23(6):1129-38. doi: 10.1007/BF00042347.
10
Constitutive, light-responsive and circadian clock-responsive factors compete for the different l box elements in plant light-regulated promoters.组成型、光响应型和生物钟响应型因子竞争植物光调控启动子中的不同l盒元件。
Plant J. 1993 Oct;4(4):611-9. doi: 10.1046/j.1365-313x.1993.04040611.x.

鉴定受光和生物钟调控的拟南芥核酮糖-1,5-二磷酸羧化酶/加氧酶激活酶(RCA)最小启动子。

Identification of an Arabidopsis thaliana ribulose-1,5-bisphosphate carboxylase/oxygenase activase (RCA) minimal promoter regulated by light and the circadian clock.

作者信息

Liu Z, Taub C C, McClung C R

机构信息

Department of Biological Sciences, Dartmouth College, Hanover, New Hampshire 03755, USA.

出版信息

Plant Physiol. 1996 Sep;112(1):43-51. doi: 10.1104/pp.112.1.43.

DOI:10.1104/pp.112.1.43
PMID:8819320
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC157921/
Abstract

Transcription of the Arabidopsis thaliana gene encoding ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) activase (RCA) is organ-specific, light-responsive, and regulated by the circadian clock. RCA is transcribed throughout the green parts of the plant, but not in roots and petals. Responses elicited by short pulses of light indicate that the light response is mediated, at least in part, by phytochrome. Analysis of transgenic tobacco and Arabidopsis carrying RCA 5' untranscribed regions fused to reporter genes (uidA, encoding beta-glucuronidase, or cat, encoding chloramphenicol acetyltransferase) indicate that elements sufficient to confer organ-specific, light-responsive, and clock-regulated transcription are localized within 317 base pairs upstream of the site of transcription initiation. A clock-responsive element sufficient to confer a low-amplitude (approximately 2-fold) circadian oscillation lies within 317 base pairs of the trascription start, but other elements necessary for high-amplitude (approximately 10-fold) circadian oscillation lie upstream of -317 and are removed by deletion from -970 to -317.

摘要

拟南芥中编码核酮糖-1,5-二磷酸羧化酶/加氧酶(Rubisco)激活酶(RCA)的基因转录具有器官特异性、光响应性,并受生物钟调控。RCA在植物的绿色部分均有转录,但在根和花瓣中不转录。短时光脉冲引发的反应表明,光反应至少部分是由光敏色素介导的。对携带与报告基因(编码β-葡萄糖醛酸酶的uidA或编码氯霉素乙酰转移酶的cat)融合的RCA 5'非转录区的转基因烟草和拟南芥的分析表明,足以赋予器官特异性、光响应性和生物钟调控转录的元件位于转录起始位点上游317个碱基对范围内。一个足以赋予低振幅(约2倍)昼夜节律振荡的生物钟响应元件位于转录起始的317个碱基对范围内,但高振幅(约10倍)昼夜节律振荡所需的其他元件位于-317上游,并且通过从-970到-317的缺失而被去除。