水稻根尖转录组分析揭示了营养生长所依赖的辅助素、赤霉素和乙烯信号。

IF 3.9 2区 生物学 Q2 CELL BIOLOGY
Kiyoshi Yamazaki, Yoshihiro Ohmori, Hirokazu Takahashi, Atsushi Toyoda, Yutaka Sato, Mikio Nakazono, Toru Fujiwara
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引用次数: 0

摘要

营养趋向性是植物根系对营养物质的积极趋向性。NH4+ 梯度是水稻(Oryza sativa L.)的一种营养刺激。当水稻根暴露于营养源周围产生的 NH4+ 梯度时,根尖会向营养源弯曲并盘绕营养源。其分子机制尚不清楚。在此,我们分析了表现出营养弯曲的根尖内部和外部的转录组,以揭示营养信号转导。我们用激光显微切割法分别采集了面向营养源(内侧)和远离营养源(外侧)的组织。主成分分析揭示了两种组织之间不同的转录组模式。对 153 个差异表达基因的注释表明,在营养生长条件下,根尖两侧的辅助素、赤霉素和乙烯信号被不同程度地激活。外源应用这些植物激素的转运和/或生物合成抑制剂在很大程度上抑制了营养生长。因此,营养生长需要这三种植物激素的信号传递和从头开始的生物合成。IAA 基因的表达模式表明,辅素在内部组织中积累较多,这意味着铵刺激在营养生长过程中与重力刺激在营养生长过程中一样,会传递给辅素信号。众所周知,SAUR 和 expansin 基因控制细胞壁的修饰,并在芽的重力营养生长过程中促进细胞伸长,但这两个基因在内侧组织而非外侧组织中高表达,我们的转录组数据无法解释根营养生长过程中的伸长差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcriptome Analysis of Rice Root Tips Reveals Auxin, Gibberellin and Ethylene Signaling Underlying Nutritropism.

Nutritropism is a positive tropism toward nutrients in plant roots. An NH4+ gradient is a nutritropic stimulus in rice (Oryza sativa L.). When rice roots are exposed to an NH4+ gradient generated around nutrient sources, root tips bend toward and coil around the sources. The molecular mechanisms are largely unknown. Here, we analyzed the transcriptomes of the inside and outside of bending root tips exhibiting nutritropism to reveal nutritropic signal transduction. Tissues facing the nutrient sources (inside) and away (outside) were separately collected by laser microdissection. Principal component analysis revealed distinct transcriptome patterns between the two tissues. Annotations of 153 differentially expressed genes implied that auxin, gibberellin and ethylene signaling were activated differentially between the sides of the root tips under nutritropism. Exogenous application of transport and/or biosynthesis inhibitors of these phytohormones largely inhibited the nutritropism. Thus, signaling and de novo biosynthesis of the three phytohormones are necessary for nutritropism. Expression patterns of IAA genes implied that auxins accumulated more in the inside tissues, meaning that ammonium stimulus is transduced to auxin signaling in nutritropism similar to gravity stimulus in gravitropism. SAUR and expansin genes, which are known to control cell wall modification and to promote cell elongation in shoot gravitropism, were highly expressed in the inside tissues rather than the outside tissues, and our transcriptome data are unexplainable for differential elongation in root nutritropism.

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来源期刊
Plant and Cell Physiology
Plant and Cell Physiology 生物-细胞生物学
CiteScore
8.40
自引率
4.10%
发文量
166
审稿时长
1.7 months
期刊介绍: Plant & Cell Physiology (PCP) was established in 1959 and is the official journal of the Japanese Society of Plant Physiologists (JSPP). The title reflects the journal''s original interest and scope to encompass research not just at the whole-organism level but also at the cellular and subcellular levels. Amongst the broad range of topics covered by this international journal, readers will find the very best original research on plant physiology, biochemistry, cell biology, molecular genetics, epigenetics, biotechnology, bioinformatics and –omics; as well as how plants respond to and interact with their environment (abiotic and biotic factors), and the biology of photosynthetic microorganisms.
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