Gil P, Green P J
MSU-DOE Plant Research Laboratory, Michigan State University, East Lansing 48824-1312, USA.
EMBO J. 1996 Apr 1;15(7):1678-86.
The small-auxin-up-RNA (SAUR) transcripts are rapidly induced by auxin and are among the most short-lived mRNAs in higher plants. In this study, we investigate the regulation of SAUR-AC1, a well characterized SAUR gene of Arabidopsis. Be examining the expression of chimeric genes in transgenic tobacco, we demonstrate that the promoter region of SAUR-AC1 mediates auxin induction. Sequences downstream of the promoter region were found to limit mRNA accumulation in a manner that was independent of auxin treatment. Both the coding region and the 3' untranslated region (UTR) of SAUR-AC1 independently contribute to this limitation. Effects on mRNA stability were assayed using chimeric genes under the control of the tetracycline-repressible Top10 promoter. mRNA half-life analysis following tetracycline treatment showed that the SAUR-AC1 coding region does not contain elements that decrease mRNA stability. In contrast, the 3' UTR was found to act as a potent mRNA instability determinant. This finding and the general utility of the Top10 system should provide the means to elucidate mRNA decay pathways that are potentially novel and specific for certain unstable transcripts.
小生长素上调RNA(SAUR)转录本会被生长素迅速诱导,并且是高等植物中寿命最短的mRNA之一。在本研究中,我们研究了拟南芥中一个特征明确的SAUR基因SAUR-AC1的调控机制。通过检测转基因烟草中嵌合基因的表达,我们证明SAUR-AC1的启动子区域介导了生长素诱导。发现启动子区域下游的序列以一种独立于生长素处理的方式限制mRNA积累。SAUR-AC1的编码区和3'非翻译区(UTR)均独立地导致了这种限制。使用四环素可抑制的Top10启动子控制下的嵌合基因来检测对mRNA稳定性的影响。四环素处理后的mRNA半衰期分析表明,SAUR-AC1编码区不包含降低mRNA稳定性的元件。相反,发现3'UTR是一个有效的mRNA不稳定决定因素。这一发现以及Top10系统的普遍实用性应该为阐明可能对某些不稳定转录本而言是新颖且特异的mRNA降解途径提供方法。