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光诱导培养植物细胞中叶绿体分化前的基因。

Light induction of genes preceding chloroplast differentiation in cultured plant cells.

机构信息

Institut für Botanik, Universität Hannover, Herrenhäuserstrasse 2, D-3000, Hannover 21, Germany.

出版信息

Planta. 1990 May;181(2):220-8. doi: 10.1007/BF02411542.

Abstract

Our aim was to identify, using their complementary DNAs (cDNAs), genes which are rapidly and transiently expressed during the initial phase of blue-light-induced chloroplast differentiation in cultured plant cells (Chenopodium rubrum L.), and to evaluate the role of their prospective products with regard to light perception, signal transduction and response, as well as coordination in the expression of other blue-light-induced genes. A cDNA library (λ gt10) was established using polyadenylated RNAs from cells exposed to blue light for 6, 12, and 24 h. Selection of the relevant species from the combined preparations was achieved by applying hybridization techniques and hydroxylapatite chromatography, thus eliminating most of the mRNAs representative of dark-grown and fully greened cells. By differential screening, several clones corresponding to genes rapidly induced by blue light were identified. For most of these a temporary accumulation of the specific mRNA between 30 min and 72 h of blue-light irradiation was observed. With regard to the nucleotide sequence and the respective deduced amino-acid sequence, a glycine-rich protein, a β-tubulin-like protein and one species resembling an acidic ribosomal protein (RLAO) were among the products of the early light-induced genes.

摘要

我们的目的是利用互补 DNA(cDNA)来鉴定在培养的植物细胞(藜)中蓝光诱导的叶绿体分化初始阶段快速和短暂表达的基因,并评估其潜在产物在光感知、信号转导和反应以及协调其他蓝光诱导基因表达方面的作用。使用暴露于蓝光 6、12 和 24 h 的多聚腺苷酸化 RNA 建立了 cDNA 文库(λgt10)。通过应用杂交技术和羟基磷灰石层析法从组合制剂中选择相关物种,从而消除了大多数代表暗生长和完全绿化细胞的 mRNA。通过差异筛选,鉴定了几个对应于蓝光快速诱导基因的克隆。对于其中大多数基因,在蓝光照射 30 分钟至 72 小时之间观察到特定 mRNA 的暂时积累。就核苷酸序列和相应推导的氨基酸序列而言,富含甘氨酸的蛋白、β-微管蛋白样蛋白和一种类似于酸性核糖体蛋白(RLAO)的物质是早期光诱导基因的产物之一。

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