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矮牵牛茎尖切段中吲哚乙酸的分布及与生长素运输、碳水化合物代谢和不定根形成的关系。

Distribution of indole-3-acetic acid in Petunia hybrida shoot tip cuttings and relationship between auxin transport, carbohydrate metabolism and adventitious root formation.

机构信息

Institute of Biological Chemistry (IBC), Washington State University, Pullman, WA 99164-6340, USA.

出版信息

Planta. 2013 Sep;238(3):499-517. doi: 10.1007/s00425-013-1907-z. Epub 2013 Jun 14.

DOI:10.1007/s00425-013-1907-z
PMID:23765266
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3751230/
Abstract

To determine the contribution of polar auxin transport (PAT) to auxin accumulation and to adventitious root (AR) formation in the stem base of Petunia hybrida shoot tip cuttings, the level of indole-3-acetic acid (IAA) was monitored in non-treated cuttings and cuttings treated with the auxin transport blocker naphthylphthalamic acid (NPA) and was complemented with precise anatomical studies. The temporal course of carbohydrates, amino acids and activities of controlling enzymes was also investigated. Analysis of initial spatial IAA distribution in the cuttings revealed that approximately 40 and 10 % of the total IAA pool was present in the leaves and the stem base as rooting zone, respectively. A negative correlation existed between leaf size and IAA concentration. After excision of cuttings, IAA showed an early increase in the stem base with two peaks at 2 and 24 h post excision and, thereafter, a decline to low levels. This was mirrored by the expression pattern of the auxin-responsive GH3 gene. NPA treatment completely suppressed the 24-h peak of IAA and severely inhibited root formation. It also reduced activities of cell wall and vacuolar invertases in the early phase of AR formation and inhibited the rise of activities of glucose-6-phosphate dehydrogenase and phosphofructokinase during later stages. We propose a model in which spontaneous AR formation in Petunia cuttings is dependent on PAT and on the resulting 24-h peak of IAA in the rooting zone, where it induces early cellular events and also stimulates sink establishment. Subsequent root development stimulates glycolysis and the pentose phosphate pathway.

摘要

为了确定极性生长素运输(PAT)对拟南芥茎尖插条生长素积累和不定根(AR)形成的贡献,监测了未经处理的插条和用生长素运输阻滞剂萘基邻氨甲酰苯甲酸(NPA)处理的插条中的吲哚-3-乙酸(IAA)水平,并进行了精确的解剖学研究。还研究了碳水化合物、氨基酸和控制酶活性的时间过程。分析插条中初始空间 IAA 分布表明,总 IAA 库中约有 40%和 10%分别存在于叶片和作为生根区的茎基部。叶片大小与 IAA 浓度之间存在负相关。在切割插条后,IAA 在茎基部早期增加,在切割后 2 和 24 小时出现两个峰值,然后下降到低水平。这与生长素响应基因 GH3 的表达模式一致。NPA 处理完全抑制了 24 小时的 IAA 峰值,并严重抑制了根的形成。它还降低了 AR 形成早期细胞壁和液泡转化酶的活性,并抑制了后期葡萄糖-6-磷酸脱氢酶和磷酸果糖激酶活性的升高。我们提出了一个模型,即拟南芥插条中自发形成的 AR 依赖于 PAT 和生根区中由此产生的 24 小时 IAA 峰值,该峰值诱导早期细胞事件,并刺激汇的建立。随后的根发育刺激糖酵解和戊糖磷酸途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/5196802f0def/425_2013_1907_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/411ebbd92606/425_2013_1907_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/f418d83b062f/425_2013_1907_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/e89ece854a73/425_2013_1907_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/e2fe4295ce31/425_2013_1907_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/b80060bea964/425_2013_1907_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/263421fcea8c/425_2013_1907_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/048d826b019f/425_2013_1907_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/007338387754/425_2013_1907_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/5196802f0def/425_2013_1907_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/411ebbd92606/425_2013_1907_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/f418d83b062f/425_2013_1907_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/e89ece854a73/425_2013_1907_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/e2fe4295ce31/425_2013_1907_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/b80060bea964/425_2013_1907_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/263421fcea8c/425_2013_1907_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/048d826b019f/425_2013_1907_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/007338387754/425_2013_1907_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ff/3751230/5196802f0def/425_2013_1907_Fig9_HTML.jpg

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