Biologisches Institut II der Universtät Freiburg, Schänzlestraße 1, D-7800, Freiburg, Federal Republic of Germany.
Planta. 1982 Mar;154(1):81-6. doi: 10.1007/BF00385501.
The steady-state levels of plastid RNA sequences in dark-grown and light-grown mustard (Sinapis alba L.) seedlings have been compared. Total cellular RNAs were labeled in vitro with (32)P and hybridized to separated restriction fragments of plastid DNA. Cloned DNA fragments which encode the large subunit (LS) of ribulose-1,5-bisphosphate carboxylase [3-phospho-D-glycerate carboxylase (dimerizing), EC 4.1.1.39] and a 35,000 plastid polypeptide were used as probes to assess the levels of these two plastid mRNAs. The 1.22-kilobase-pair mRNA for the 35,000 polypeptide is almost undetectable in dark-grown seedlings, but is a major plastid mRNA in light-grown seedlings. The hybridization analysis of RNA from seedlings which were irradiated with red and far-red light indicates that the level of this mRNA, but not of LS mRNA, is controlled by phytochrome.
已经比较了暗培养和光培养芥菜(Sinapis alba L.)幼苗中质体 RNA 序列的稳定水平。用(32)P 在体外标记总细胞 RNA,并与质体 DNA 的分离限制片段杂交。用作探针的克隆 DNA 片段编码核酮糖-1,5-二磷酸羧化酶的大亚基(LS)[3-磷酸-D-甘油酸羧化酶(二聚体),EC 4.1.1.39]和 35,000 个质体多肽,以评估这两种质体 mRNA 的水平。在黑暗培养的幼苗中,1.22kbp 的 35,000 多肽 mRNA 几乎无法检测到,但在光培养的幼苗中是主要的质体 mRNA。用红光和远红光照射的幼苗的 RNA 的杂交分析表明,这种 mRNA 的水平,但不是 LS mRNA 的水平,受光敏色素控制。