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在猴肾COS细胞中,丝心蛋白基因转录的忠实且高效起始仅需要TATA盒和帽位点区域。

In monkey COS cells only the TATA box and the cap site region are required for faithful and efficient initiation of the fibroin gene transcription.

作者信息

Tokunaga K, Hirose S, Suzuki Y

出版信息

Nucleic Acids Res. 1984 Feb 10;12(3):1543-58. doi: 10.1093/nar/12.3.1543.

DOI:10.1093/nar/12.3.1543
PMID:6322109
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC318595/
Abstract

The DNA sequences necessary for faithful and efficient initiation of transcription of Bombyx mori fibroin gene have been studied in vivo using monkey COS cells and a SV40 origin vector. Transcriptional analysis of 5' deletion genes and of exact substitution genes including a series of single base substitution mutants indicates that the TATA box and the cap region are required for faithful and efficient initiation of the fibroin gene transcription in vivo, whereas far upstream sequences and the CAAT-like sequences are not required. In addition, single base substitution genes of the cap site region have clearly shown that there exists a strict sequence requirement of the cap region of the fibroin gene. These results define the basic promoter of the fibroin gene to the region spanning the TATA box and the cap site region.

摘要

利用猴COS细胞和SV40起始载体在体内研究了家蚕丝心蛋白基因忠实高效转录起始所需的DNA序列。对5'缺失基因以及包括一系列单碱基取代突变体在内的精确取代基因进行转录分析表明,TATA框和帽区是家蚕丝心蛋白基因在体内忠实高效转录起始所必需的,而远上游序列和类CAAT序列则不是必需的。此外,帽位点区域的单碱基取代基因清楚地表明,丝心蛋白基因的帽区存在严格的序列要求。这些结果将丝心蛋白基因的基本启动子定义为跨越TATA框和帽位点区域的区域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eaa6/318595/84ca35c6ad6f/nar00321-0259-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eaa6/318595/2e73552f9827/nar00321-0255-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eaa6/318595/fbdadf836478/nar00321-0256-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eaa6/318595/84ca35c6ad6f/nar00321-0259-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eaa6/318595/2e73552f9827/nar00321-0255-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eaa6/318595/fbdadf836478/nar00321-0256-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eaa6/318595/84ca35c6ad6f/nar00321-0259-a.jpg

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1
In monkey COS cells only the TATA box and the cap site region are required for faithful and efficient initiation of the fibroin gene transcription.在猴肾COS细胞中,丝心蛋白基因转录的忠实且高效起始仅需要TATA盒和帽位点区域。
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2
trans repression of the human metallothionein IIA gene promoter by PZ120, a novel 120-kilodalton zinc finger protein.新型120千道尔顿锌指蛋白PZ120对人金属硫蛋白IIA基因启动子的反式抑制作用
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本文引用的文献

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Chromatin structure: deduced from a minichromosome.染色质结构:从小染色体推断出来的。
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Faithful transcription initiation of fibroin gene in a homologous cell-free system reveals an enhancing effect of 5' flanking sequence far upstream.在同源无细胞系统中丝心蛋白基因的忠实转录起始揭示了远上游5'侧翼序列的增强作用。
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An RNA polymerase II promoter containing sequences upstream and downstream from the RNA startpoint that direct initiation of transcription from the same site.一种RNA聚合酶II启动子,其包含RNA起始点上游和下游的序列,这些序列指导从同一位点起始转录。
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Functional dissection of a mouse ribosomal protein promoter: significance of the polypyrimidine initiator and an element in the TATA-box region.小鼠核糖体蛋白启动子的功能剖析:多嘧啶起始子及TATA框区域中一个元件的意义
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A contribution of the core-promoter and its surrounding regions to the preferential transcription of the fibroin gene in posterior silk gland extracts.核心启动子及其周边区域对后部丝腺提取物中丝素基因优先转录的贡献。
EMBO J. 1990 Feb;9(2):489-96. doi: 10.1002/j.1460-2075.1990.tb08135.x.
基本腺病毒E1A功能的表达不需要TATA同源序列和mRNA 5'非翻译序列。
Cell. 1982 May;29(1):139-48. doi: 10.1016/0092-8674(82)90098-8.
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Nature. 1982 Jul 8;298(5870):192-5. doi: 10.1038/298192a0.
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In vitro characterization of the fibroin gene promoter by the use of single-base substitution mutants.利用单碱基取代突变体对丝心蛋白基因启动子进行体外特性分析。
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Promoter sequence of fibroin gene assigned by in vitro transcription system.通过体外转录系统确定的丝心蛋白基因启动子序列。
Proc Natl Acad Sci U S A. 1981 Aug;78(8):4838-42. doi: 10.1073/pnas.78.8.4838.
7
Spacer DNA sequences upstream of the T-A-T-A-A-A-T-A sequence are essential for promotion of H2A histone gene transcription in vivo.T-A-T-A-A-A-T-A序列上游的间隔DNA序列对于体内H2A组蛋白基因转录的促进至关重要。
Proc Natl Acad Sci U S A. 1980 Dec;77(12):7102-6. doi: 10.1073/pnas.77.12.7102.
8
Identification of regulatory sequences in the prelude sequences of an H2A histone gene by the study of specific deletion mutants in vivo.通过对体内特定缺失突变体的研究鉴定H2A组蛋白基因前奏序列中的调控序列。
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Cell. 1982 Sep;30(2):517-28. doi: 10.1016/0092-8674(82)90249-5.
10
Purification of mouse immunoglobulin heavy-chain messenger RNAs from total myeloma tumor RNA.从小鼠骨髓瘤肿瘤总RNA中纯化小鼠免疫球蛋白重链信使RNA。
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