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生长素应答mRNA的诱导及超诱导与生长素和蛋白质合成抑制剂的关系

Induction and superinduction of auxin-responsive mRNAs with auxin and protein synthesis inhibitors.

作者信息

Franco A R, Gee M A, Guilfoyle T J

机构信息

Department of Biochemistry, University of Missouri, Columbia 65211.

出版信息

J Biol Chem. 1990 Sep 15;265(26):15845-9.

PMID:2394751
Abstract

We have identified a class of small mRNAs (approximately 0.5 kilobases), referred to as small auxin-up RNAs (SAURs), that increases in abundance within minutes after auxin application to excised elongating hypocotyl sections of soybean. In this study, we present evidence that SAURs accumulate in the absence of auxin when protein synthesis is inhibited. Superinduction of SAURs occurs if the synthetic auxin 2,4-dichlorophenoxyacetic acid is added under conditions where protein synthesis is inhibited. Transcription run-on experiments with isolated nuclei show that, unlike 2,4-dichlorophenoxyacetic acid, protein synthesis inhibitors do not activate transcription of the SAUR genes. These results suggest that protein synthesis inhibitors act by stabilizing SAURs and that some labile protein(s) are involved in the rapid turnover of SAURs. This stabilization is not observed with GH3, another auxin-inducible mRNA. Whether induced with 2,4-dichlorophenoxyacetic acid or cycloheximide, SAURs are primarily expressed in epidermal and cortical cells of elongating hypocotyl sections, with little or no expression in vascular tissue. Unlike 2,4-dichlorophenoxyacetic acid-induced SAUR accumulation, the increase in abundance of SAURs induced by cycloheximide is transient, with a peak approximately 1 h after inhibitor addition. Complete inhibition of protein synthesis is not required for SAUR accumulation in the presence of protein synthesis inhibitors.

摘要

我们已经鉴定出一类小mRNA(约0.5千碱基),称为小生长素上调RNA(SAURs),在生长素施加到切除的大豆伸长下胚轴切段后几分钟内其丰度增加。在本研究中,我们提供证据表明,当蛋白质合成受到抑制时,SAURs在没有生长素的情况下积累。如果在蛋白质合成受到抑制的条件下添加合成生长素2,4-二氯苯氧乙酸,SAURs会发生超诱导。用分离的细胞核进行的转录延伸实验表明,与2,4-二氯苯氧乙酸不同,蛋白质合成抑制剂不会激活SAUR基因的转录。这些结果表明,蛋白质合成抑制剂通过稳定SAURs起作用,并且一些不稳定的蛋白质参与了SAURs的快速周转。用另一种生长素诱导的mRNA即GH3未观察到这种稳定作用。无论用2,4-二氯苯氧乙酸还是放线菌酮诱导,SAURs主要在伸长的下胚轴切段的表皮和皮层细胞中表达,在维管组织中几乎不表达或不表达。与2,4-二氯苯氧乙酸诱导的SAUR积累不同,放线菌酮诱导的SAURs丰度增加是短暂的,在添加抑制剂后约1小时达到峰值。在存在蛋白质合成抑制剂的情况下,SAUR积累不需要完全抑制蛋白质合成。

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