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本文引用的文献

1
Duplication and quadruplication of Arabidopsis thaliana cysteinyl- and asparaginyl-tRNA synthetase genes of organellar origin.拟南芥细胞器来源的半胱氨酰和天冬氨酰tRNA合成酶基因的重复和四倍化
J Mol Evol. 2000 May;50(5):413-23. doi: 10.1007/s002390010044.
2
Regulation of plastid rDNA transcription by interaction of CDF2 with two different RNA polymerases.通过CDF2与两种不同RNA聚合酶的相互作用对质体rDNA转录进行调控。
EMBO J. 2000 Apr 17;19(8):1851-60. doi: 10.1093/emboj/19.8.1851.
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Identification and characterization of T3/T7 bacteriophage-like RNA polymerase sequences in wheat.小麦中T3/T7噬菌体样RNA聚合酶序列的鉴定与表征
Plant Mol Biol. 1999 Jul;40(4):567-78. doi: 10.1023/a:1006203928189.
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Targeted disruption of the plastid RNA polymerase genes rpoA, B and C1: molecular biology, biochemistry and ultrastructure.质体RNA聚合酶基因rpoA、B和C1的靶向破坏:分子生物学、生物化学及超微结构
Plant J. 1999 Jun;18(5):477-89. doi: 10.1046/j.1365-313x.1999.00473.x.
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Organellar RNA polymerases of higher plants.高等植物的细胞器RNA聚合酶。
Int Rev Cytol. 1999;190:1-59. doi: 10.1016/s0074-7696(08)62145-2.
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Functional analysis of two maize cDNAs encoding T7-like RNA polymerases.两个编码T7样RNA聚合酶的玉米cDNA的功能分析。
Plant Cell. 1999 May;11(5):911-26. doi: 10.1105/tpc.11.5.911.
7
Green fluorescent protein as a marker to investigate targeting of organellar RNA polymerases of higher plants in vivo.绿色荧光蛋白作为一种标记物,用于在体内研究高等植物细胞器RNA聚合酶的靶向作用。
Plant J. 1999 Mar;17(5):557-61. doi: 10.1046/j.1365-313x.1999.00393.x.
8
In vitro characterization of the tobacco rpoB promoter reveals a core sequence motif conserved between phage-type plastid and plant mitochondrial promoters.烟草rpoB启动子的体外特性分析揭示了噬菌体型质体启动子与植物线粒体启动子之间保守的核心序列基序。
EMBO J. 1999 Jan 4;18(1):249-57. doi: 10.1093/emboj/18.1.249.
9
Characterization of a gene encoding a single-subunit bacteriophage-type RNA polymerase from maize which is alternatively spliced.对来自玉米的一个编码单亚基噬菌体型RNA聚合酶且可选择性剪接的基因的表征。
Mol Gen Genet. 1998 Oct;260(1):30-7. doi: 10.1007/s004380050867.
10
Mitochondrial protein import in plants. Signals, sorting, targeting, processing and regulation.植物中的线粒体蛋白导入。信号、分选、靶向、加工与调控。
Plant Mol Biol. 1998 Sep;38(1-2):311-38. doi: 10.1023/a:1006020208140.

一种RNA聚合酶服务于两个基因组。

One RNA polymerase serving two genomes.

作者信息

Hedtke B, Börner T, Weihe A

机构信息

Institut für Biologie, Abteilung Genetik, Humboldt-Universität zu Berlin, Germany.

出版信息

EMBO Rep. 2000 Nov;1(5):435-40. doi: 10.1093/embo-reports/kvd086.

DOI:10.1093/embo-reports/kvd086
PMID:11258484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1083759/
Abstract

The land plant Arabidopsis thaliana contains three closely related nuclear genes encoding phage-type RNA polymerases (RpoT;1, RpoT;2 and RpoT;3). The gene products of RpoT;1 and RpoT;3 have previously been shown to be imported into mitochondria and chloroplasts, respectively. Here we show that the transit peptide of RpoT;2 possesses dual targeting properties. Transient expression assays in tobacco protoplasts as well as stable transformation of Arabidopsis plants demonstrate efficient targeting of fusion peptides consisting of the N-terminus of RpoT;2 joined to green fluorescent protein to both organelles. Thus, RpoT;2 might be the first RNA polymerase shown to transcribe genes in two different genomes. RNA polymerase activity of recombinant RpoT;2 is uneffected by the inhibitor tagetin, qualifying the gene product of RpoT;2 as a phage-type polymerase.

摘要

陆地植物拟南芥含有三个密切相关的核基因,它们编码噬菌体类型的RNA聚合酶(RpoT;1、RpoT;2和RpoT;3)。先前已证明RpoT;1和RpoT;3的基因产物分别被导入线粒体和叶绿体。在这里,我们表明RpoT;2的转运肽具有双重靶向特性。烟草原生质体中的瞬时表达分析以及拟南芥植物的稳定转化表明,由RpoT;2的N端与绿色荧光蛋白连接而成的融合肽能够有效地靶向这两种细胞器。因此,RpoT;2可能是首个被证明能在两个不同基因组中转录基因的RNA聚合酶。重组RpoT;2的RNA聚合酶活性不受抑制剂塔格汀的影响,这表明RpoT;2的基因产物是一种噬菌体类型的聚合酶。