Suppr超能文献

苹果ACC氧化酶和多聚半乳糖醛酸酶:转基因番茄中成熟特异性基因表达及启动子分析

Apple ACC-oxidase and polygalacturonase: ripening-specific gene expression and promoter analysis in transgenic tomato.

作者信息

Atkinson R G, Bolitho K M, Wright M A, Iturriagagoitia-Bueno T, Reid S J, Ross G S

机构信息

Horticultural Research Institute of New Zealand, Mt Albert Research Centre, Auckland.

出版信息

Plant Mol Biol. 1998 Oct;38(3):449-60. doi: 10.1023/a:1006065926397.

Abstract

Levels of 1-aminocyclopropane-1-carboxylate (ACC) oxidase and polygalacturonase (PG) mRNAs were characterized during ripening of Royal Gala, Braeburn and Granny Smith apples. Both ACC-oxidase and PG mRNAs were up-regulated in ripening fruit of all three cultivars. Expression in Royal Gala was detected earlier than in Braeburn and Granny Smith, relative to internal ethylene concentration. Genomic clones corresponding to the ACC-oxidase and PG mRNAs expressed in ripe apple fruit were isolated and ca. 2 kb of each promoter was sequenced. The start point of transcription in each gene was mapped by primer extension, and sequences homologous to elements in other ethylene-responsive or PG promoters were identified. The fruit specificity of the apple ACC-oxidase and PG promoters was investigated in transgenic tomato plants using a nested set of promoter fragments fused to the beta-glucuronidase (gusA) reporter gene. For the ACC-oxidase gene, 450 bp of 5' promoter sequence was sufficient to drive GUS expression, although this expression was not specific to ripening fruit. Larger fragments of 1966 and 1159 bp showed both fruit and ripening specificity. For the PG gene, promoter fragments of 1460 and 532 bp conferred ripening-specific expression in transgenic tomato fruit. However GUS expression was down-regulated by 2356 bp of promoter, suggesting the presence of a negative regulatory element between positions -1460 and -2356.

摘要

在皇家嘎啦、澳洲青苹和布瑞本苹果成熟过程中,对1-氨基环丙烷-1-羧酸(ACC)氧化酶和多聚半乳糖醛酸酶(PG)的mRNA水平进行了表征。在这三个品种的成熟果实中,ACC氧化酶和PG的mRNA均上调。相对于内部乙烯浓度,皇家嘎啦果实中的表达比澳洲青苹和布瑞本苹果中更早被检测到。分离出了与成熟苹果果实中表达的ACC氧化酶和PG的mRNA相对应的基因组克隆,并对每个启动子约2 kb的序列进行了测序。通过引物延伸确定了每个基因的转录起始点,并鉴定了与其他乙烯响应或PG启动子中的元件同源的序列。使用与β-葡萄糖醛酸酶(gusA)报告基因融合的一系列嵌套启动子片段,在转基因番茄植株中研究了苹果ACC氧化酶和PG启动子的果实特异性。对于ACC氧化酶基因,5'端450 bp的启动子序列足以驱动GUS表达,尽管这种表达并非果实成熟所特有。1966 bp和1159 bp的较大片段则显示出果实和成熟特异性。对于PG基因,1460 bp和532 bp的启动子片段在转基因番茄果实中赋予了成熟特异性表达。然而,2356 bp的启动子使GUS表达下调,这表明在-1460至-2356位之间存在一个负调控元件。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验