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菠菜中质体蓝素单拷贝基因和叶绿体ATP合酶δ亚基启动子的分析。

Analysis of the promotors of the single-copy genes for plastocyanin and subunit delta of the chloroplast ATP synthase from spinach.

作者信息

Bichler J, Herrmann R G

机构信息

Botanisches Institut, Ludwig-Maximilians-Universität München, Federal Republic of Germany.

出版信息

Eur J Biochem. 1990 Jun 20;190(2):415-26. doi: 10.1111/j.1432-1033.1990.tb15591.x.

Abstract

The promotors of the single-copy genes for subunit delta of the chloroplast ATP synthase (atpD) and plastocyanin (PC) from spinach have been sequenced, dissected and analysed in transgenic F0 and F1 tobacco plants using the bacterial GUS gene as a reporter for promotor activity. The transcription of these genes is photo-controlled. The results have been compared with those obtained for the spinach rbcS-1 gene, one of the light-regulated genes encoding the small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase, and for the cauliflower mosaic virus (CaMV) 35S RNA promotor. We find that the 5' upstream regions of about 1200 nucleotides contain all the sequences required for light regulation, organ-, tissue- and development-specific expression, and that they are structurally diverse. Their cis-acting elements are functionally defined. The proximal regions of the spinach promotors contain potential TATA, CAAT and T-cyt boxes at appropriate positions, but only sequence elements with low similarity to published light-responsive elements. Positive light-stimulated regions, regions with constitutive, light-independent enhancing effects and with 'silencer'-like activity in complete darkness are found in proximal and far upstream promotor segments. Highest activity of these promotors is correlated with the presence of chloroplasts but is not confined to photosynthetic tissue. Surprisingly, expression is observed in the phloem regions of transgenic leaves, leaf and floral stems, in the vascular area of anthers and in pollen. No histochemical staining has been detected in roots. The distal region of atpD located between -1137 and -590 contains elements for expression in the outer phloem, the region from -590 to -185 for activity in the inner phloem of floral stems. Similar tissue-specific patterns are observed with a fusion between the caufliflower mosaic virus 35S RNA promotor and the GUS gene.

摘要

对菠菜叶绿体ATP合酶δ亚基(atpD)和质体蓝素(PC)单拷贝基因的启动子进行了测序,并在转基因F0和F1烟草植株中利用细菌GUS基因作为启动子活性的报告基因进行了剖析和分析。这些基因的转录受光控制。将结果与菠菜rbcS - 1基因(编码核酮糖-1,5-二磷酸羧化酶/加氧酶小亚基的光调节基因之一)以及花椰菜花叶病毒(CaMV)35S RNA启动子的结果进行了比较。我们发现,约1200个核苷酸的5'上游区域包含光调节、器官、组织和发育特异性表达所需的所有序列,并且它们在结构上是多样的。其顺式作用元件在功能上已被确定。菠菜启动子的近端区域在适当位置含有潜在的TATA、CAAT和T - 胞嘧啶盒,但与已发表的光响应元件只有低相似性的序列元件。在近端和远上游启动子片段中发现了正的光刺激区域、具有组成型、光不依赖增强作用以及在完全黑暗中具有“沉默子”样活性的区域。这些启动子的最高活性与叶绿体的存在相关,但不限于光合组织。令人惊讶的是,在转基因叶片的韧皮部区域、叶和花茎、花药的维管区域以及花粉中观察到了表达。在根中未检测到组织化学染色。位于-1137和-590之间的atpD远端区域包含在外韧皮部表达的元件,从-590到-185的区域在花茎的内韧皮部具有活性。用花椰菜花叶病毒35S RNA启动子与GUS基因的融合体也观察到了类似的组织特异性模式。

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