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真核生物tRNA基因的体外转录。I. 使用竞争分析对调控区的分析。

Transcription of eukaryotic tRNA genes in vitro. I. Analysis of control regions using a competition assay.

作者信息

Sharp S, Dingermann T, Schaack J, DeFranco D, Söll D

出版信息

J Biol Chem. 1983 Feb 25;258(4):2440-6.

PMID:6549757
Abstract

The regions of a Drosophila tRNAArg gene responsible for the "wild type" in vitro transcription level were determined by a transcription-competition assay. Cell-free transcription extracts programmed with 5' and 3' deletion mutants of the tRNAArg gene were used to quantitate the efficiency of transcription and to measure the ability of these DNAs to compete for transcription factors compared to the wild type tRNAArg gene. The results show that those portions of the gene which code for the D-stem/D-loop and T-stem/T-loop of the tRNA product are the regions responsible for competitive ability. These regions were previously shown to contain the intragenic control sequences for eukaryotic tRNA gene transcription and are respectively referred to as the D- and T-control regions. The presence of both the D- and T-control regions is essential for maximum competitive strength. The 5'-flanking and 5' stem regions adjacent to the D-control region have a function in the competitive ability of the D-control region while the 3'-flanking and the 3' stem regions adjacent to the T-control region have a function in the competitive ability of the T-control region. These results are consistent with a model for promotion of tRNA gene transcription that involves recognition by transcription factors of the two control regions. Optimal binding of the transcription factors is dependent upon sequences adjacent to and flanking the intragenic control regions.

摘要

通过转录竞争试验确定了果蝇tRNAArg基因中负责“野生型”体外转录水平的区域。用tRNAArg基因的5'和3'缺失突变体编程的无细胞转录提取物用于定量转录效率,并测量这些DNA与野生型tRNAArg基因相比竞争转录因子的能力。结果表明,该基因中编码tRNA产物的D茎/D环和T茎/T环的部分是负责竞争能力的区域。这些区域先前已被证明含有真核tRNA基因转录的基因内控制序列,分别称为D控制区和T控制区。D控制区和T控制区的同时存在对于最大竞争强度至关重要。与D控制区相邻的5'侧翼和5'茎区在D控制区的竞争能力中起作用,而与T控制区相邻的3'侧翼和3'茎区在T控制区的竞争能力中起作用。这些结果与一种促进tRNA基因转录的模型一致,该模型涉及转录因子对两个控制区的识别。转录因子的最佳结合取决于基因内控制区相邻和侧翼的序列。

相似文献

1
Transcription of eukaryotic tRNA genes in vitro. I. Analysis of control regions using a competition assay.真核生物tRNA基因的体外转录。I. 使用竞争分析对调控区的分析。
J Biol Chem. 1983 Feb 25;258(4):2440-6.
2
The minimum intragenic sequences required for promotion of eukaryotic tRNA gene transcription.促进真核生物tRNA基因转录所需的最小基因内序列。
Nucleic Acids Res. 1982 Sep 25;10(18):5393-406. doi: 10.1093/nar/10.18.5393.
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Stable transcription complex formation of eukaryotic tRNA genes is dependent on a limited separation of the two intragenic control regions.真核生物tRNA基因稳定转录复合体的形成依赖于两个基因内控制区域的有限分离。
J Biol Chem. 1983 Sep 10;258(17):10395-402.
4
Transcription of eukaryotic tRNA genes in vitro. II. Formation of stable complexes.真核生物tRNA基因的体外转录。II. 稳定复合物的形成
J Biol Chem. 1983 Feb 25;258(4):2447-53.
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Each element of the Drosophila tRNAArg gene split promoter directs transcription in Xenopus oocytes.果蝇tRNA精氨酸基因分裂启动子的每个元件都能在非洲爪蟾卵母细胞中指导转录。
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Internal control regions for transcription of eukaryotic tRNA genes.真核生物tRNA基因转录的内部控制区域。
Proc Natl Acad Sci U S A. 1981 Nov;78(11):6657-61. doi: 10.1073/pnas.78.11.6657.
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The 5- flanking sequences of Drosophila tRNAArg genes control their in vitro transcription in a Drosophila cell extract.果蝇tRNA精氨酸基因的5'侧翼序列在果蝇细胞提取物中控制其体外转录。
J Biol Chem. 1982 Dec 25;257(24):14738-44.
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Transcription factor binding is limited by the 5'-flanking regions of a Drosophila tRNAHis gene and a tRNAHis pseudogene.转录因子结合受果蝇组氨酸转运RNA基因和组氨酸转运RNA假基因的5'侧翼区域限制。
Mol Cell Biol. 1984 Dec;4(12):2714-22. doi: 10.1128/mcb.4.12.2714-2722.1984.
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Eukaryotic tRNA gene transcription is controlled by signals within and outside the mature coding sequence.真核生物转运RNA基因的转录受成熟编码序列内外信号的控制。
Princess Takamatsu Symp. 1982;12:63-72.
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The extent of a eukaryotic tRNA gene. 5'- and 3'-flanking sequence dependence for transcription and stable complex formation.真核生物tRNA基因的范围。转录和稳定复合物形成对5'和3'侧翼序列的依赖性。
J Biol Chem. 1984 Feb 10;259(3):1461-7.

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