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乙烯与芽再生:无钩1调控拟南芥从头芽器官发生

Ethylene and shoot regeneration: hookless1 modulates de novo shoot organogenesis in Arabidopsis thaliana.

作者信息

Chatfield Steven P, Raizada Manish N

机构信息

Department of Plant Agriculture, University of Guelph, Guelph, ON, Canada, N1G 2W1.

出版信息

Plant Cell Rep. 2008 Apr;27(4):655-66. doi: 10.1007/s00299-007-0496-3. Epub 2007 Dec 15.

Abstract

We have investigated the role of ethylene in shoot regeneration from cotyledon explants of Arabidopsis thaliana. We examined the ethylene sensitivity of five ecotypes representing both poor and prolific shoot regenerators and identified Dijon-G, a poor regenerator, as an ecotype with dramatically enhanced ethylene sensitivity. However, inhibiting ethylene action with silver nitrate generally reduced shoot organogenesis in ecotypes capable of regeneration. In ecotype Col-0, we found that ethylene-insensitive mutants (etr1-1, ein2-1, ein4, ein7) exhibited reduced shoot regeneration rates, whereas constitutive ethylene response mutants (ctr1-1, ctr1-12) increased the proportion of explants producing shoots. Our experiments with ethylene over-production mutants (eto1, eto2 and eto3) indicate that the ethylene biosynthesis inhibitor gene, ETO1, can act as an inhibitor of shoot regeneration. Pharmacological elevation of ethylene levels was also found to significantly increase the proportion of explants regenerating shoots. We determined that the hookless1 (hls1-1) mutant, a suppressor of the ethylene response phenotypes of ctr1 and eto1 mutants, is capable of dramatically enhancing shoot organogenesis. The effects of ACC and loss of HLS1 function on shoot organogenesis were found to be largely additive.

摘要

我们研究了乙烯在拟南芥子叶外植体芽再生中的作用。我们检测了代表再生能力差和再生能力强的5个生态型的乙烯敏感性,确定再生能力差的第戎-G生态型是乙烯敏感性显著增强的生态型。然而,用硝酸银抑制乙烯作用通常会降低能够再生的生态型中的芽器官发生。在生态型Col-0中,我们发现乙烯不敏感突变体(etr1-1、ein2-1、ein4、ein7)的芽再生率降低,而组成型乙烯反应突变体(ctr1-1、ctr1-12)增加了产生芽的外植体比例。我们对乙烯过量产生突变体(eto1、eto2和eto3)的实验表明,乙烯生物合成抑制基因ETO1可作为芽再生的抑制剂。还发现通过药理学方法提高乙烯水平可显著增加再生芽的外植体比例。我们确定,钩状蛋白1(hls1-1)突变体是ctr1和eto1突变体乙烯反应表型的抑制子,能够显著增强芽器官发生。发现ACC和HLS1功能缺失对芽器官发生的影响在很大程度上是累加的。

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