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人7S K DNA在体外和体内的转录完全由一个上游启动子控制。

Transcription of human 7S K DNA in vitro and in vivo is exclusively controlled by an upstream promoter.

作者信息

Kleinert H, Benecke B J

机构信息

Lehrstuhl für Biochemie, Ruhr-Universität, FRG.

出版信息

Nucleic Acids Res. 1988 Feb 25;16(4):1319-31. doi: 10.1093/nar/16.4.1319.

DOI:10.1093/nar/16.4.1319
PMID:2450332
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC336317/
Abstract

We have analyzed the transcription of a recently isolated human 7S K RNA gene in vitro and in vivo. In contrast to hitherto characterized class III genes (genes transcribed by RNA polymerase III), the coding sequence of this gene is not required for faithful and efficient transcription by RNA polymerase III. In fact, a procaryotic vector DNA sequence was efficiently transcribed by RNA polymerase III under the control of the 7S K RNA gene upstream sequence in vitro and in vivo. S1-nuclease protection analyses confirmed that the 7S K 5'flanking sequence was sufficient for accurate transcription initiation. These data demonstrate that 7S K DNA represents a novel class III gene, the promoter elements of which are located outside the coding sequence.

摘要

我们已经分别在体外和体内对最近分离出的人类7S K RNA基因的转录情况进行了分析。与迄今已鉴定的III类基因(由RNA聚合酶III转录的基因)不同,该基因的编码序列对于RNA聚合酶III进行准确且高效的转录并非必需。事实上,在体外和体内,原核载体DNA序列在7S K RNA基因上游序列的控制下,都能被RNA聚合酶III高效转录。S1核酸酶保护分析证实,7S K 5'侧翼序列足以实现精确的转录起始。这些数据表明,7S K DNA代表了一种新型的III类基因,其启动子元件位于编码序列之外。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3506/336317/9b21ce2ec9cc/nar00146-0105-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3506/336317/1ac39fe8eb1e/nar00146-0102-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3506/336317/31868db0e277/nar00146-0104-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3506/336317/9b21ce2ec9cc/nar00146-0105-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3506/336317/1ac39fe8eb1e/nar00146-0102-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3506/336317/31868db0e277/nar00146-0104-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3506/336317/9b21ce2ec9cc/nar00146-0105-a.jpg

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引用本文的文献

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2
Two internal sequence elements modulate transcription from the external human 7S K RNA gene promoter in vivo.两个内部序列元件在体内调节人源外部7S K RNA基因启动子的转录。
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3
A highly specific terminal uridylyl transferase modifies the 3'-end of U6 small nuclear RNA.一种高度特异性的末端尿苷酰转移酶修饰U6小核RNA的3'末端。

本文引用的文献

1
Transcriptional control regions of the adenovirus VAI RNA gene.腺病毒VAI RNA基因的转录控制区域。
Cell. 1980 Nov;22(2 Pt 2):405-13. doi: 10.1016/0092-8674(80)90351-7.
2
Multiple factors are required for the accurate transcription of purified genes by RNA polymerase III.RNA聚合酶III对纯化基因进行准确转录需要多种因素。
J Biol Chem. 1980 Dec 25;255(24):11986-91.
3
Reinitiation of synthesis of small cytoplasmic RNA species K and L in isolated HeLa cell nuclei in vitro.体外分离的HeLa细胞核中小细胞质RNA种类K和L合成的重新起始
Nucleic Acids Res. 1998 Jul 1;26(13):3119-26. doi: 10.1093/nar/26.13.3119.
4
Perspectives in cancer chemoprevention.癌症化学预防的前景
Environ Health Perspect. 1997 Jun;105 Suppl 4(Suppl 4):945-54. doi: 10.1289/ehp.97105s4945.
5
BC1 RNA: transcriptional analysis of a neural cell-specific RNA polymerase III transcript.BC1 RNA:一种神经细胞特异性RNA聚合酶III转录本的转录分析
Mol Cell Biol. 1995 Mar;15(3):1642-50. doi: 10.1128/MCB.15.3.1642.
6
The seemingly identical 7SK and U6 core promoters depend on different transcription factor complexes.看似相同的7SK和U6核心启动子依赖于不同的转录因子复合物。
Gene Expr. 1993;3(2):175-85.
7
Transcription of a human U6 small nuclear RNA gene in vivo withstands deletion of intragenic sequences but not of an upstream TATATA box.人U6小核RNA基因在体内的转录能够耐受基因内序列的缺失,但不能耐受上游TATATA框的缺失。
Nucleic Acids Res. 1989 Sep 25;17(18):7371-9. doi: 10.1093/nar/17.18.7371.
8
Amplification of plant U3 and U6 snRNA gene sequences using primers specific for an upstream promoter element and conserved intragenic regions.使用针对上游启动子元件和保守基因内区域的引物扩增植物U3和U6小核RNA基因序列。
Nucleic Acids Res. 1990 Jun 25;18(12):3459-66. doi: 10.1093/nar/18.12.3459.
9
U6 snRNA genes of Arabidopsis are transcribed by RNA polymerase III but contain the same two upstream promoter elements as RNA polymerase II-transcribed U-snRNA genes.拟南芥的U6小核RNA基因由RNA聚合酶III转录,但含有与RNA聚合酶II转录的U小核RNA基因相同的两个上游启动子元件。
Nucleic Acids Res. 1990 Jun 25;18(12):3451-8. doi: 10.1093/nar/18.12.3451.
10
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。
Proc Natl Acad Sci U S A. 1990 Jun;87(11):4289-93. doi: 10.1073/pnas.87.11.4289.
Nucleic Acids Res. 1980 Jan 25;8(2):225-34. doi: 10.1093/nar/8.2.225.
4
A control region in the center of the 5S RNA gene directs specific initiation of transcription: II. The 3' border of the region.5S RNA基因中心的一个控制区域指导转录的特异性起始:II. 该区域的3'边界。
Cell. 1980 Jan;19(1):27-35. doi: 10.1016/0092-8674(80)90385-2.
5
A control region in the center of the 5S RNA gene directs specific initiation of transcription: I. The 5' border of the region.5S RNA基因中心的一个控制区域指导转录的特异性起始:I. 该区域的5'边界。
Cell. 1980 Jan;19(1):13-25. doi: 10.1016/0092-8674(80)90384-0.
6
Two conserved sequence blocks within eukaryotic tRNA genes are major promoter elements.真核生物tRNA基因中的两个保守序列块是主要的启动子元件。
Nature. 1981 Dec 17;294(5842):626-31. doi: 10.1038/294626a0.
7
A split promoter for a eucaryotic tRNA gene.一种真核生物tRNA基因的分裂启动子。
Cell. 1981 May;24(2):573-85. doi: 10.1016/0092-8674(81)90348-2.
8
The binding of a transcription factor to deletion mutants of a 5S ribosomal RNA gene.转录因子与5S核糖体RNA基因缺失突变体的结合。
Cell. 1981 Mar;23(3):665-9. doi: 10.1016/0092-8674(81)90429-3.
9
Promoter of a eukaryotic tRNAPro gene is composed of three noncontiguous regions.真核生物tRNAPro基因的启动子由三个不连续的区域组成。
Proc Natl Acad Sci U S A. 1982 Feb;79(4):1195-9. doi: 10.1073/pnas.79.4.1195.
10
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.