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本文引用的文献

1
Naturally occurring auxin transport regulators.天然存在的生长素运输调节剂。
Science. 1988 Jul 15;241(4863):346-9. doi: 10.1126/science.241.4863.346.
2
Immunophilin-like TWISTED DWARF1 modulates auxin efflux activities of Arabidopsis P-glycoproteins.类亲免素扭曲矮化蛋白1调节拟南芥P-糖蛋白的生长素外排活性。
J Biol Chem. 2006 Oct 13;281(41):30603-12. doi: 10.1074/jbc.M604604200. Epub 2006 Aug 3.
3
High-affinity auxin transport by the AUX1 influx carrier protein.由AUX1内流载体蛋白介导的高亲和力生长素运输。
Curr Biol. 2006 Jun 6;16(11):1123-7. doi: 10.1016/j.cub.2006.04.029. Epub 2006 May 4.
4
Acyltransferases in plants: a good time to be BAHD.植物中的酰基转移酶:成为BAHD家族成员的黄金时期
Curr Opin Plant Biol. 2006 Jun;9(3):331-40. doi: 10.1016/j.pbi.2006.03.016. Epub 2006 Apr 17.
5
Polar PIN localization directs auxin flow in plants.极性PIN定位引导植物中的生长素流动。
Science. 2006 May 12;312(5775):883. doi: 10.1126/science.1121356. Epub 2006 Apr 6.
6
PIN proteins perform a rate-limiting function in cellular auxin efflux.PIN蛋白在细胞生长素外流中发挥限速功能。
Science. 2006 May 12;312(5775):914-8. doi: 10.1126/science.1123542. Epub 2006 Apr 6.
7
A coumaroyl-ester-3-hydroxylase insertion mutant reveals the existence of nonredundant meta-hydroxylation pathways and essential roles for phenolic precursors in cell expansion and plant growth.一个香豆酰酯-3-羟化酶插入突变体揭示了非冗余间位羟基化途径的存在以及酚类前体在细胞扩张和植物生长中的重要作用。
Plant Physiol. 2006 Jan;140(1):30-48. doi: 10.1104/pp.105.069690. Epub 2005 Dec 23.
8
Cellular efflux of auxin catalyzed by the Arabidopsis MDR/PGP transporter AtPGP1.由拟南芥MDR/PGP转运蛋白AtPGP1催化的生长素细胞外排。
Plant J. 2005 Oct;44(2):179-94. doi: 10.1111/j.1365-313X.2005.02519.x.
9
Reassessment of effects on lignification and vascular development in the irx4 Arabidopsis mutant.对拟南芥irx4突变体中木质化和维管发育影响的重新评估。
Phytochemistry. 2005 Sep;66(17):2092-107. doi: 10.1016/j.phytochem.2004.12.016.
10
Inhibition of P-glycoprotein by natural products in human breast cancer cells.天然产物对人乳腺癌细胞中P-糖蛋白的抑制作用。
Arch Pharm Res. 2005 Jul;28(7):823-8. doi: 10.1007/BF02977349.

拟南芥中木质素合成受抑制时类黄酮的积累会影响生长素运输和植物生长。

Flavonoid accumulation in Arabidopsis repressed in lignin synthesis affects auxin transport and plant growth.

作者信息

Besseau Sébastien, Hoffmann Laurent, Geoffroy Pierrette, Lapierre Catherine, Pollet Brigitte, Legrand Michel

机构信息

Institut de Biologie Moléculaire des Plantes, Laboratoire Propre du Centre National de la Recherche Scientifique, Unité Propre de Recherche 2357, Conventioné à l'Université Louis Pasteur, 67000 Strasbourg, France.

出版信息

Plant Cell. 2007 Jan;19(1):148-62. doi: 10.1105/tpc.106.044495. Epub 2007 Jan 19.

DOI:10.1105/tpc.106.044495
PMID:17237352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1820963/
Abstract

In Arabidopsis thaliana, silencing of hydroxycinnamoyl-CoA shikimate/quinate hydroxycinnamoyl transferase (HCT), a lignin biosynthetic gene, results in a strong reduction of plant growth. We show that, in HCT-silenced plants, lignin synthesis repression leads to the redirection of the metabolic flux into flavonoids through chalcone synthase activity. Several flavonol glycosides and acylated anthocyanin were shown to accumulate in higher amounts in silenced plants. By contrast, sinapoylmalate levels were barely affected, suggesting that the synthesis of that phenylpropanoid compound might be HCT-independent. The growth phenotype of HCT-silenced plants was shown to be controlled by light and to depend on chalcone synthase expression. Histochemical analysis of silenced stem tissues demonstrated altered tracheary elements. The level of plant growth reduction of HCT-deficient plants was correlated with the inhibition of auxin transport. Suppression of flavonoid accumulation by chalcone synthase repression in HCT-deficient plants restored normal auxin transport and wild-type plant growth. By contrast, the lignin structure of the plants simultaneously repressed for HCT and chalcone synthase remained as severely altered as in HCT-silenced plants, with a large predominance of nonmethoxylated H units. These data demonstrate that the reduced size phenotype of HCT-silenced plants is not due to the alteration of lignin synthesis but to flavonoid accumulation.

摘要

在拟南芥中,木质素生物合成基因羟基肉桂酰辅酶A莽草酸/奎尼酸羟基肉桂酰转移酶(HCT)的沉默导致植物生长显著减缓。我们发现,在HCT沉默的植物中,木质素合成的抑制通过查尔酮合酶活性导致代谢通量转向类黄酮。几种黄酮醇糖苷和酰化花青素在沉默植物中积累量更高。相比之下,芥子酰苹果酸水平几乎不受影响,这表明该苯丙烷类化合物的合成可能不依赖于HCT。HCT沉默植物的生长表型受光照控制,并依赖于查尔酮合酶的表达。对沉默茎组织的组织化学分析表明管状分子发生了改变。HCT缺陷型植物的生长减缓水平与生长素运输的抑制相关。在HCT缺陷型植物中通过抑制查尔酮合酶来抑制类黄酮积累可恢复正常的生长素运输和野生型植物生长。相比之下,同时抑制HCT和查尔酮合酶的植物的木质素结构仍与HCT沉默植物一样严重改变,非甲氧基化H单元占主导。这些数据表明,HCT沉默植物的体型变小表型不是由于木质素合成的改变,而是由于类黄酮的积累。