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本文引用的文献

1
Auxin controls petal initiation in Arabidopsis.生长素控制拟南芥花瓣的起始。
Development. 2013 Jan 1;140(1):185-94. doi: 10.1242/dev.084582. Epub 2012 Nov 22.
2
A regulatory network for coordinated flower maturation.一个协调花成熟的调控网络。
PLoS Genet. 2012 Feb;8(2):e1002506. doi: 10.1371/journal.pgen.1002506. Epub 2012 Feb 9.
3
SHINE transcription factors act redundantly to pattern the archetypal surface of Arabidopsis flower organs.SHINE 转录因子冗余性地作用以塑造拟南芥花器官的典型表面模式。
PLoS Genet. 2011 May;7(5):e1001388. doi: 10.1371/journal.pgen.1001388. Epub 2011 May 26.
4
A member of the PLEIOTROPIC DRUG RESISTANCE family of ATP binding cassette transporters is required for the formation of a functional cuticle in Arabidopsis.多效耐药相关的 ATP 结合盒转运蛋白家族的一个成员对于拟南芥功能性表皮的形成是必需的。
Plant Cell. 2011 May;23(5):1958-70. doi: 10.1105/tpc.111.083121. Epub 2011 May 31.
5
The plant cuticle is required for osmotic stress regulation of abscisic acid biosynthesis and osmotic stress tolerance in Arabidopsis.植物角质层对于拟南芥脱落酸生物合成和渗透胁迫耐受的渗透胁迫调节是必需的。
Plant Cell. 2011 May;23(5):1971-84. doi: 10.1105/tpc.110.081943. Epub 2011 May 24.
6
LEUNIG and SEUSS co-repressors regulate miR172 expression in Arabidopsis flowers.LEUNIG 和 SEUSS 共抑制子调控拟南芥花中 miR172 的表达。
Development. 2011 Jun;138(12):2451-6. doi: 10.1242/dev.058362.
7
AUXIN RESPONSE FACTOR8 regulates Arabidopsis petal growth by interacting with the bHLH transcription factor BIGPETALp.生长素响应因子 8 通过与 bHLH 转录因子 BIGPETALp 相互作用调节拟南芥花瓣生长。
Plant Cell. 2011 Mar;23(3):973-83. doi: 10.1105/tpc.110.081653. Epub 2011 Mar 18.
8
The biophysical design of plant cuticles: an overview.植物表皮的生物物理设计:概述。
New Phytol. 2011 Mar;189(4):938-49. doi: 10.1111/j.1469-8137.2010.03553.x.
9
The Arabidopsis ABCG13 transporter is required for flower cuticle secretion and patterning of the petal epidermis.拟南芥 ABCG13 转运蛋白是花表皮角质层分泌和花瓣表皮模式形成所必需的。
New Phytol. 2011 Apr;190(1):113-124. doi: 10.1111/j.1469-8137.2010.03608.x. Epub 2011 Jan 14.
10
Arabidopsis auxin response factor6 and 8 regulate jasmonic acid biosynthesis and floral organ development via repression of class 1 KNOX genes.拟南芥生长素反应因子 6 和 8 通过抑制类 1 KNOX 基因调控茉莉酸生物合成和花器官发育。
Plant Cell Physiol. 2010 Jan;51(1):164-75. doi: 10.1093/pcp/pcp176. Epub 2009 Dec 10.

花器官的物理相互作用控制拟南芥花瓣的形态发生。

Physical interaction of floral organs controls petal morphogenesis in Arabidopsis.

机构信息

Department of Botany, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.

出版信息

Plant Physiol. 2013 Mar;161(3):1242-50. doi: 10.1104/pp.112.212084. Epub 2013 Jan 11.

DOI:10.1104/pp.112.212084
PMID:23314942
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3585593/
Abstract

Flowering plants bear beautiful flowers to attract pollinators. Petals are the most variable organs in flowering plants, with their color, fragrance, and shape. In Arabidopsis (Arabidopsis thaliana), petal primordia arise at a similar time to stamen primordia and elongate at later stages through the narrow space between anthers and sepals. Although many of the genes involved in regulating petal identity and primordia growth are known, the molecular mechanism for the later elongation process remains unknown. We found a mutant, folded petals1 (fop1), in which normal petal development is inhibited during their growth through the narrow space between sepals and anthers, resulting in formation of folded petals at maturation. During elongation, the fop1 petals contact the sepal surface at several sites. The conical-shaped petal epidermal cells are flattened in the fop1 mutant, as if they had been pressed from the top. Surgical or genetic removal of sepals in young buds restores the regular growth of petals, suggesting that narrow space within a bud is the cause of petal folding in the fop1 mutant. FOP1 encodes a member of the bifunctional wax ester synthase/diacylglycerol acyltransferase family, WSD11, which is expressed in elongating petals and localized to the plasma membrane. These results suggest that the FOP1/WSD11 products synthesized in the petal epidermis may act as a lubricant, enabling uninhibited growth of the petals as they extend between the sepals and the anthers.

摘要

开花植物开出美丽的花朵来吸引传粉者。花瓣是开花植物中最具变化的器官,其颜色、香味和形状各不相同。在拟南芥(Arabidopsis thaliana)中,花瓣原基与雄蕊原基在相似的时间出现,并在后期通过雄蕊和萼片之间的狭窄空间伸长。尽管已知许多参与调节花瓣身份和原基生长的基因,但后期伸长过程的分子机制仍不清楚。我们发现了一个突变体,折叠花瓣 1(fop1),在该突变体中,正常花瓣在通过萼片和雄蕊之间的狭窄空间生长时被抑制,导致成熟时形成折叠花瓣。在伸长过程中,fop1 花瓣在几个部位与萼片表面接触。在 fop1 突变体中,锥形花瓣表皮细胞被压平,就好像它们是从顶部被压平的。在幼芽中进行萼片的外科或遗传去除可恢复花瓣的正常生长,这表明芽内的狭窄空间是 fop1 突变体中花瓣折叠的原因。FOP1 编码双功能蜡酯合酶/二酰基甘油酰基转移酶家族的成员 WSD11,该基因在伸长的花瓣中表达,并定位于质膜。这些结果表明,在花瓣表皮中合成的 FOP1/WSD11 产物可能充当润滑剂,使花瓣在向萼片和雄蕊延伸时能够不受抑制地生长。