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蓝光对培养植物细胞中两种质体 mRNA 水平的调控。

Blue light control of the level of two plastid mRNAs in cultured plant cells.

机构信息

Institut für Botanik, Universität Hannover, Herrenhäuserstraße 2, D-3000, Hannover 1, F.R.G..

出版信息

Plant Mol Biol. 1984 Sep;3(5):271-6. doi: 10.1007/BF00017780.

Abstract

In suspension cultured callus cells of tobacco (Nicotiana tabacum var. 'Samsun') the development of chloroplasts is strictly blue light-dependent. During this process chlorophylls and other pigments as well as membrane and stroma proteins are synthesized de-novo. Cloned chloroplast genes of mustard encoding the large subunit (LSU) of ribulosebisphosphate carboxylase/oxygenase (EC. 4.1.1.39; RuBPCase) and the precursor polypeptide of the 32-kD membrane protein were used to study the effect of blue light on the steady-state concentration of the complementary mRNA sequences. For both a rapid increase in dark-grown cells in response to blue light-irradiation was detected by RNA dot-hybridization technique. The time courses coincide with those previously elucidated for the synthesis rates of both LSU and the membrane protein. The results support the notion that blue light acts primarily through mRNA induction.

摘要

在烟草(Nicotiana tabacum var. 'Samsun')悬浮培养的愈伤组织细胞中,叶绿体的发育严格依赖蓝光。在此过程中,叶绿素和其他色素以及膜和基质蛋白都是从头合成的。克隆的芥菜叶绿体基因编码核酮糖-1,5-二磷酸羧化酶/加氧酶(EC.4.1.1.39;RuBPCase)的大亚基(LSU)和 32kD 膜蛋白的前体多肽,用于研究蓝光对互补 mRNA 序列的稳态浓度的影响。通过 RNA 斑点杂交技术,在黑暗中生长的细胞在受到蓝光照射时,迅速增加,这一点得到了检测。时间过程与先前阐明的 LSU 和膜蛋白的合成速率相吻合。这些结果支持了蓝光主要通过 mRNA 诱导起作用的观点。

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