Meir Shimon, Hunter Donald A, Chen Jen-Chih, Halaly Vita, Reid Michael S
Department of Postharvest Science of Fresh Produce, Agricultural Research Organization, The Volcani Center, Bet Dagan 50250, Israel.
Plant Physiol. 2006 Aug;141(4):1604-16. doi: 10.1104/pp.106.079277. Epub 2006 Jun 15.
To understand how auxin regulates sensitivity of abscission zone (AZ) tissues to ethylene, we used a polymerase chain reaction-based subtractive approach to identify gene transcripts in Mirabilis jalapa AZs that changed in abundance during the time the zones became competent to abscise in response to exogenous ethylene. Transcript expression was then examined in leaf and stem AZs over the period they became ethylene competent following indole-3-acetic acid (IAA) depletion either by leaf deblading, treatment with the IAA transport inhibitor naphthylphthalamic acid, or cutting the stem above a node (decapitation). Transcripts down-regulated by deblading/decapitation included Mj-Aux/IAA1 and Mj-Aux/IAA2, encoding Aux/IAA proteins, and three other transcripts showing highest identity to a polygalacturonase inhibitor protein, a beta-expansin, and a beta-tubulin. Application of IAA to the cut end of petioles or stumps inhibited abscission, and prevented the decline in the levels of transcripts in both AZs. Transcripts up-regulated in the AZ following deblading/decapitation or treatment with naphthylphthalamic acid were isolated from plants pretreated with 1-methylcyclopropene before deblading to help select against ethylene-induced genes. Some of the up-regulated transcripts showed identity to proteins associated with ethylene or stress responses, while others did not show homology to known sequences. Sucrose infiltration of stem stumps enhanced abscission following ethylene treatment and also enhanced the induction of some of the up-regulated genes. Our results demonstrate a correlation between acquisition of competence to respond to ethylene in both leaf and stem AZs, and decline in abundance of auxin regulatory gene transcripts.
为了解生长素如何调节离层区(AZ)组织对乙烯的敏感性,我们采用基于聚合酶链反应的消减方法,来鉴定紫茉莉AZ中在该区域因外源乙烯而具备脱落能力期间丰度发生变化的基因转录本。然后,在通过去叶、用生长素运输抑制剂萘基邻苯二甲酸处理或在节上方切割茎(断头)使吲哚 - 3 - 乙酸(IAA)耗尽后,叶和茎AZ在具备乙烯响应能力的期间检测转录本表达。去叶/断头下调的转录本包括编码Aux/IAA蛋白的Mj - Aux/IAA1和Mj - Aux/IAA2,以及另外三个与多聚半乳糖醛酸酶抑制蛋白、β - 扩张蛋白和β - 微管蛋白具有最高同源性的转录本。将IAA施加到叶柄或树桩的切割端可抑制脱落,并防止两个AZ中转录本水平的下降。从去叶前用1 - 甲基环丙烯预处理的植物中分离出去叶/断头或用萘基邻苯二甲酸处理后在AZ中上调的转录本,以帮助筛选出乙烯诱导的基因。一些上调的转录本与乙烯或应激反应相关的蛋白质具有同源性,而其他转录本与已知序列没有同源性。茎树桩的蔗糖浸润增强了乙烯处理后的脱落,也增强了一些上调基因的诱导。我们的结果表明,叶和茎AZ中获得对乙烯响应的能力与生长素调节基因转录本丰度的下降之间存在相关性。