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本文引用的文献

1
PIFs: pivotal components in a cellular signaling hub.PIFs:细胞信号枢纽中的关键组成部分。
Trends Plant Sci. 2011 Jan;16(1):19-28. doi: 10.1016/j.tplants.2010.08.003. Epub 2010 Sep 20.
2
SPATULA links daytime temperature and plant growth rate.SPATULA 关联日温与植物生长速率。
Curr Biol. 2010 Aug 24;20(16):1493-7. doi: 10.1016/j.cub.2010.07.028. Epub 2010 Aug 12.
3
Transcriptional diversification and functional conservation between DELLA proteins in Arabidopsis.拟南芥中 DELLA 蛋白的转录多样化和功能保守性。
Mol Biol Evol. 2010 Jun;27(6):1247-56. doi: 10.1093/molbev/msq012. Epub 2010 Jan 21.
4
The bHLH transcription factor SPATULA controls final leaf size in Arabidopsis thaliana.bHLH 转录因子 SPATULA 控制拟南芥的最终叶片大小。
Plant Cell Physiol. 2010 Feb;51(2):252-61. doi: 10.1093/pcp/pcp184. Epub 2009 Dec 29.
5
Definition of early transcriptional circuitry involved in light-induced reversal of PIF-imposed repression of photomorphogenesis in young Arabidopsis seedlings.早期转录电路在光诱导的拟南芥幼苗中 PIF 介导的光形态建成抑制的逆转中的作用。
Plant Cell. 2009 Nov;21(11):3535-53. doi: 10.1105/tpc.109.070672. Epub 2009 Nov 17.
6
Obituary: Norman E. Borlaug (1914-2009).讣告:诺曼·E·博洛格(1914 - 2009)。
Nature. 2009 Oct 15;461(7266):894. doi: 10.1038/461894a.
7
Phytochrome functions in Arabidopsis development.光敏色素在拟南芥发育中的功能。
J Exp Bot. 2010;61(1):11-24. doi: 10.1093/jxb/erp304.
8
Phytochrome interacting factors 4 and 5 redundantly limit seedling de-etiolation in continuous far-red light.光敏色素相互作用因子 4 和 5 在连续远红光中冗余地限制幼苗去黄化。
Plant J. 2009 Nov;60(3):449-61. doi: 10.1111/j.1365-313X.2009.03971.x. Epub 2009 Jul 8.
9
Gibberellin signaling in the endodermis controls Arabidopsis root meristem size.内皮层中的赤霉素信号传导控制拟南芥根分生组织的大小。
Curr Biol. 2009 Jul 28;19(14):1194-9. doi: 10.1016/j.cub.2009.06.023. Epub 2009 Jul 2.
10
Gibberellin signaling controls cell proliferation rate in Arabidopsis.赤霉素信号传导调控拟南芥中的细胞增殖速率。
Curr Biol. 2009 Jul 28;19(14):1188-93. doi: 10.1016/j.cub.2009.05.059. Epub 2009 Jul 2.

伪装的 DELLA:SPATULA 抑制拟南芥幼苗的生长。

A DELLA in disguise: SPATULA restrains the growth of the developing Arabidopsis seedling.

机构信息

School of Biological Sciences, Institute of Molecular Plant Sciences, University of Edinburgh, Edinburgh EH93JH, United Kingdom.

出版信息

Plant Cell. 2011 Apr;23(4):1337-51. doi: 10.1105/tpc.110.082594. Epub 2011 Apr 8.

DOI:10.1105/tpc.110.082594
PMID:21478445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3101537/
Abstract

The period following seedling emergence is a particularly vulnerable stage in the plant life cycle. In Arabidopsis thaliana, the phytochrome-interacting factor (PIF) subgroup of basic-helix-loop-helix transcription factors has a pivotal role in regulating growth during this early phase, integrating environmental and hormonal signals. We previously showed that SPATULA (SPT), a PIF homolog, regulates seed dormancy. In this article, we establish that unlike PIFs, which mainly promote hypocotyl elongation, SPT is a potent regulator of cotyledon expansion. Here, SPT acts in an analogous manner to the gibberellin-dependent DELLAs, REPRESSOR OF GA1-3 and GIBBERELLIC ACID INSENSITIVE, which restrain cotyledon expansion alongside SPT. However, although DELLAs are not required for SPT action, we demonstrate that SPT is subject to negative regulation by DELLAs. Cross-regulation of SPT by DELLAs ensures that SPT protein levels are limited when DELLAs are abundant but rise following DELLA depletion. This regulation provides a means to prevent excessive growth suppression that would result from the dual activity of SPT and DELLAs, yet maintain growth restraint under DELLA-depleted conditions. We present evidence that SPT and DELLAs regulate common gene targets and illustrate that the balance of SPT and DELLA action depends on light quality signals in the natural environment.

摘要

幼苗出土后的时期是植物生命周期中特别脆弱的阶段。在拟南芥中,光受体相互作用因子(PIF)亚组的碱性螺旋-环-螺旋转录因子在早期生长调控中发挥着关键作用,整合环境和激素信号。我们之前曾表明,PIF 同源物 SPATULA(SPT)调节种子休眠。在本文中,我们确定 SPT 不同于主要促进下胚轴伸长的 PIFs,而是子叶扩张的有力调节因子。在这里,SPT 以类似于赤霉素依赖的 DELLAs 的方式发挥作用,REPRESSOR OF GA1-3 和 GIBBERELLIC ACID INSENSITIVE,与 SPT 一起限制子叶扩张。然而,尽管 DELLAs 不是 SPT 作用所必需的,但我们证明 SPT 受 DELLAs 的负调控。DELLAs 对 SPT 的交叉调节确保了当 DELLAs 丰富时 SPT 蛋白水平受到限制,但在 DELLA 耗尽后 SPT 蛋白水平上升。这种调节提供了一种防止由于 SPT 和 DELLAs 的双重活性而导致的过度生长抑制的方法,但在 DELLA 耗尽的条件下仍维持生长抑制。我们提出了 SPT 和 DELLAs 调节共同靶基因的证据,并说明了 SPT 和 DELLA 作用的平衡取决于自然环境中的光质信号。