AUXIN-BINDING-PROTEIN1 (ABP1) in phytochrome-B-controlled responses.

AUXIN-BINDING-PROTEIN1 (ABP1) in phytochrome-B-controlled responses.
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DOI:
10.1093/jxb/ert294
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发表时间:
2013-11
影响因子:
6.9
通讯作者:
Scherer GF
Scherer GF
中科院分区:
生物学1区
文献类型:
--
作者:
Effendi Y;Jones AM;Scherer GF

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生长素受体ABP1直接调节质膜活性,包括PIN形成蛋白的数量和生长素的外流运输。由光敏色素介导的红光(R)调节黄化组织中ABP1的稳态水平和生长素诱导的生长能力,但到目前为止,还没有遗传证据表明ABP1和光敏色素对器官伸长的调节具有共同的机制。在远红光下,abp1-5和abp1/abp1突变体的下胚轴长度较长,而运输抑制反应生长素受体的零突变体TIR1-1的下胚轴长度不变。生长素运输抑制剂萘基邻苯二甲酸(NPA)对伸长的抑制作用在低R:FR光照条件下比在高红:FR光照条件下更明显,这表明生长素运输是FR诱导伸长的重要条件。与野生型下胚轴相比,在富含R和FR的光下生长的下胚轴中加入NPA对下胚轴向重力性的抑制程度在abp1突变体中更大,在abp1突变体中与生长素运输相关的光敏色素作用减弱。富含FR的光诱导基因,包括几个受生长素和遮荫调控的基因,在abp1-5中的转录水平比Col低3-5倍,在abp1/abp1中的转录水平很低。在PhyB-9突变体中,这些报告基因在TIR1-1中的表达比在Col1-1中低5-15倍,而PhyA-211突变体的遮荫诱导基因表达明显减弱。因此,ABP1直接或间接参与生长素和光信号转导。
The auxin receptor ABP1 directly regulates plasma membrane activities including the number of PIN-formed (PIN) proteins and auxin efflux transport. Red light (R) mediated by phytochromes regulates the steady-state level of ABP1 and auxin-inducible growth capacity in etiolated tissues but, until now, there has been no genetic proof that ABP1 and phytochrome regulation of elongation share a common mechanism for organ elongation. In far red (FR)-enriched light, hypocotyl lengths were larger in the abp1-5 and abp1/ABP1 mutants, but not in tir1-1, a null mutant of the TRANSPORT-INHIBITOR-RESPONSE1 auxin receptor. The polar auxin transport inhibitor naphthylphthalamic acid (NPA) decreased elongation in the low R:FR light-enriched white light (WL) condition more strongly than in the high red:FR light-enriched condition WL suggesting that auxin transport is an important condition for FR-induced elongation. The addition of NPA to hypocotyls grown in R- and FR-enriched light inhibited hypocotyl gravitropism to a greater extent in both abp1 mutants and in phyB-9 and phyA-211 than the wild-type hypocotyl, arguing for decreased phytochrome action in conjunction with auxin transport in abp1 mutants. Transcription of FR-enriched light-induced genes, including several genes regulated by auxin and shade, was reduced 3-5-fold in abp1-5 compared with Col and was very low in abp1/ABP1. In the phyB-9 mutant the expression of these reporter genes was 5–15-fold lower than in Col. In tir1-1 and the phyA-211 mutants shade-induced gene expression was greatly attenuated. Thus, ABP1 directly or indirectly participates in auxin and light signalling.
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