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1
Metazoan rDNA enhancer acts by making more genes transcriptionally active.后生动物核糖体DNA增强子通过使更多基因具有转录活性来发挥作用。
J Cell Biol. 1996 Jun;133(5):943-54. doi: 10.1083/jcb.133.5.943.
2
Faithful in vivo transcription termination of Xenopus laevis rDNA. Correlation of electron microscopic spread preparations with S1 transcript analysis.非洲爪蟾核糖体DNA在体内的忠实转录终止。电子显微镜铺展制备与S1转录本分析的相关性。
Chromosoma. 1991 Dec;101(4):222-30. doi: 10.1007/BF00365154.
3
The enhancers and promoters of the Xenopus laevis ribosomal spacer are associated with histones upon active transcription of the ribosomal genes.非洲爪蟾核糖体间隔区的增强子和启动子在核糖体基因活跃转录时与组蛋白相关联。
Nucleic Acids Res. 1990 Nov 11;18(21):6393-7. doi: 10.1093/nar/18.21.6393.
4
Ribosomal gene promoter domains can function as artificial enhancers of RNA polymerase I transcription, supporting a promoter origin for natural enhancers in Xenopus.核糖体基因启动子结构域可作为RNA聚合酶I转录的人工增强子,这支持了非洲爪蟾中天然增强子的启动子起源。
Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):464-8. doi: 10.1073/pnas.91.2.464.
5
The Xenopus ribosomal DNA 60- and 81-base-pair repeats are position-dependent enhancers that function at the establishment of the preinitiation complex: analysis in vivo and in an enhancer-responsive in vitro system.非洲爪蟾核糖体DNA的60碱基对和81碱基对重复序列是位置依赖性增强子,在起始前复合物形成时发挥作用:体内分析及在增强子反应性体外系统中的分析
Mol Cell Biol. 1989 Nov;9(11):5093-104. doi: 10.1128/mcb.9.11.5093-5104.1989.
6
Transactivation of the Xenopus rRNA gene promoter by its enhancer.非洲爪蟾rRNA基因启动子被其增强子反式激活。
Nature. 1989 Oct 19;341(6243):657-9. doi: 10.1038/341657a0.
7
Virtually the entire Xenopus laevis rDNA multikilobase intergenic spacer serves to stimulate polymerase I transcription.实际上,非洲爪蟾的整个核糖体DNA多千碱基基因间隔区都用于刺激聚合酶I转录。
J Biol Chem. 1996 Oct 25;271(43):27138-45. doi: 10.1074/jbc.271.43.27138.
8
Upstream domains of the Xenopus laevis rDNA promoter are revealed in microinjected oocytes.非洲爪蟾核糖体DNA启动子的上游结构域在显微注射的卵母细胞中被揭示。
Mol Cell Biol. 1986 Apr;6(4):1228-34. doi: 10.1128/mcb.6.4.1228-1234.1986.
9
Readthrough enhancement and promoter occlusion on the ribosomal genes of Xenopus laevis.非洲爪蟾核糖体基因上的通读增强和启动子阻遏
Biochem Cell Biol. 1992 May;70(5):324-31. doi: 10.1139/o92-050.
10
A 140-base-pair repetitive sequence element in the mouse rRNA gene spacer enhances transcription by RNA polymerase I in a cell-free system.小鼠rRNA基因间隔区中的一个140个碱基对的重复序列元件在无细胞系统中增强了RNA聚合酶I的转录作用。
Proc Natl Acad Sci U S A. 1990 Oct;87(19):7527-31. doi: 10.1073/pnas.87.19.7527.

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1
Regulation of RNA Polymerase I Stability and Function.RNA聚合酶I稳定性与功能的调控
Cancers (Basel). 2022 Nov 24;14(23):5776. doi: 10.3390/cancers14235776.
2
A Deconvolution Protocol for ChIP-Seq Reveals Analogous Enhancer Structures on the Mouse and Human Ribosomal RNA Genes.一种用于ChIP-Seq的反卷积方案揭示了小鼠和人类核糖体RNA基因上类似的增强子结构。
G3 (Bethesda). 2018 Jan 4;8(1):303-314. doi: 10.1534/g3.117.300225.
3
Mouse ribosomal RNA genes contain multiple differentially regulated variants.小鼠核糖体RNA基因包含多个差异调控的变体。
PLoS One. 2008 Mar 26;3(3):e1843. doi: 10.1371/journal.pone.0001843.
4
Tor pathway regulates Rrn3p-dependent recruitment of yeast RNA polymerase I to the promoter but does not participate in alteration of the number of active genes.Tor信号通路调控酵母RNA聚合酶I在启动子上依赖Rrn3p的募集,但不参与活性基因数量的改变。
Mol Biol Cell. 2004 Feb;15(2):946-56. doi: 10.1091/mbc.e03-08-0594. Epub 2003 Oct 31.
5
In exponentially growing Saccharomyces cerevisiae cells, rRNA synthesis is determined by the summed RNA polymerase I loading rate rather than by the number of active genes.在指数生长的酿酒酵母细胞中,核糖体RNA(rRNA)的合成取决于RNA聚合酶I的总装载速率,而非活性基因的数量。
Mol Cell Biol. 2003 Mar;23(5):1558-68. doi: 10.1128/MCB.23.5.1558-1568.2003.
6
RPD3 is required for the inactivation of yeast ribosomal DNA genes in stationary phase.RPD3是静止期酵母核糖体DNA基因失活所必需的。
EMBO J. 2002 Sep 16;21(18):4959-68. doi: 10.1093/emboj/cdf498.
7
Positive feedback in eukaryotic gene networks: cell differentiation by graded to binary response conversion.真核基因网络中的正反馈:通过从分级响应转换为二元响应实现细胞分化
EMBO J. 2001 May 15;20(10):2528-35. doi: 10.1093/emboj/20.10.2528.
8
Survey and summary: transcription by RNA polymerases I and III.综述与总结:RNA聚合酶I和III介导的转录
Nucleic Acids Res. 2000 Mar 15;28(6):1283-98. doi: 10.1093/nar/28.6.1283.
9
Variegated expression of the endogenous immunoglobulin heavy-chain gene in the absence of the intronic locus control region.在内含子基因座控制区缺失的情况下内源性免疫球蛋白重链基因的斑驳表达。
Mol Cell Biol. 1999 Oct;19(10):7031-40. doi: 10.1128/MCB.19.10.7031.
10
Transcriptional activity and chromatin structure of enhancer-deleted rRNA genes in Saccharomyces cerevisiae.酿酒酵母中增强子缺失的rRNA基因的转录活性和染色质结构。
Mol Cell Biol. 1999 Jul;19(7):4953-60. doi: 10.1128/MCB.19.7.4953.

本文引用的文献

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Interaction between an acidic activator and transcription factor TFIIB is required for transcriptional activation.转录激活需要酸性激活剂与转录因子TFIIB之间的相互作用。
Nature. 1993 Jun 24;363(6431):741-4. doi: 10.1038/363741a0.
2
In vitro definition of the yeast RNA polymerase I enhancer.酵母RNA聚合酶I增强子的体外定义
Mol Cell Biol. 1993 May;13(5):2644-54. doi: 10.1128/mcb.13.5.2644-2654.1993.
3
Initiation of transcription by RNA polymerase II: a multi-step process.RNA聚合酶II启动转录:一个多步骤过程。
Prog Nucleic Acid Res Mol Biol. 1993;44:67-108. doi: 10.1016/s0079-6603(08)60217-2.
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Functional analysis of Arabidopsis thaliana rRNA gene and spacer promoters in vivo and by transient expression.拟南芥rRNA基因和间隔区启动子在体内及瞬时表达中的功能分析
Proc Natl Acad Sci U S A. 1993 Aug 15;90(16):7528-32. doi: 10.1073/pnas.90.16.7528.
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The terminal balls characteristic of eukaryotic rRNA transcription units in chromatin spreads are rRNA processing complexes.染色质铺展中真核生物rRNA转录单元特有的末端球是rRNA加工复合体。
Genes Dev. 1993 Aug;7(8):1609-19. doi: 10.1101/gad.7.8.1609.
6
Ribosomal gene promoter domains can function as artificial enhancers of RNA polymerase I transcription, supporting a promoter origin for natural enhancers in Xenopus.核糖体基因启动子结构域可作为RNA聚合酶I转录的人工增强子,这支持了非洲爪蟾中天然增强子的启动子起源。
Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):464-8. doi: 10.1073/pnas.91.2.464.
7
xUBF, an RNA polymerase I transcription factor, binds crossover DNA with low sequence specificity.xUBF是一种RNA聚合酶I转录因子,它以低序列特异性结合交叉DNA。
Mol Cell Biol. 1994 May;14(5):2871-82. doi: 10.1128/mcb.14.5.2871-2882.1994.
8
The RNA polymerase I transcription factor UBF is a sequence-tolerant HMG-box protein that can recognize structured nucleic acids.RNA聚合酶I转录因子UBF是一种序列耐受性HMG盒蛋白,能够识别结构化核酸。
Nucleic Acids Res. 1994 Jul 11;22(13):2651-7. doi: 10.1093/nar/22.13.2651.
9
Increased recruitment of TATA-binding protein to the promoter by transcriptional activation domains in vivo.转录激活结构域在体内增加TATA结合蛋白与启动子的结合。
Science. 1994 Oct 14;266(5183):280-2. doi: 10.1126/science.7939664.
10
Binding of basal transcription factor TFIIH to the acidic activation domains of VP16 and p53.基础转录因子TFIIH与VP16和p53的酸性激活结构域的结合。
Mol Cell Biol. 1994 Oct;14(10):7013-24. doi: 10.1128/mcb.14.10.7013-7024.1994.

后生动物核糖体DNA增强子通过使更多基因具有转录活性来发挥作用。

Metazoan rDNA enhancer acts by making more genes transcriptionally active.

作者信息

Osheim Y N, Mougey E B, Windle J, Anderson M, O'Reilly M, Miller O L, Beyer A, Sollner-Webb B

机构信息

Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.

出版信息

J Cell Biol. 1996 Jun;133(5):943-54. doi: 10.1083/jcb.133.5.943.

DOI:10.1083/jcb.133.5.943
PMID:8655586
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2120851/
Abstract

Enhancers could, in principle, function by increasing the rate of reinitiation on individual adjacent active promoters or by increasing the probability that an adjacent promoter is activated for transcription. We have addressed this issue for the repetitive metazoan rDNA enhancer by microinjecting Xenopus oocytes with enhancer-less and enhancer-bearing genes and determining by EM the frequency that each gene type forms active transcription units and their transcript density. We use conditions where transcription requires the normal rDNA promoter and is stimulated 30-50-fold by the enhancer. (In contrast, at saturating template conditions as used in previous EM studies, an aberrant mode of transcription is activated that is not affected by the rDNA enhancer or by the generally recognized rDNA promoter). The active transcription units on enhancer-less genes are found to be as densely packed with nascent transcripts and polymerases as those on enhancer-bearing genes and on the endogenous rRNA genes. Significantly, the enhancer-bearing genes are approximately 30-50-fold more likely to form such active transcription units than enhancer-less genes, consistent with their amounts of transcript. Complementary studies confirm that the enhancer does not affect elongation rate, the stability of the transcription complex, or transcript half-life. These data demonstrate that the repetitive metazoan rDNA enhancer causes more genes to be actively transcribed and does not alter the reinitiation rate on individual active genes.

摘要

原则上,增强子可以通过提高单个相邻活性启动子上的重新起始速率,或者通过增加相邻启动子被激活进行转录的概率来发挥作用。我们通过向非洲爪蟾卵母细胞显微注射无增强子基因和含增强子基因,并通过电子显微镜确定每种基因类型形成活性转录单位的频率及其转录本密度,来研究后生动物重复rDNA增强子的这个问题。我们使用的条件是转录需要正常的rDNA启动子,并且增强子可将其刺激30 - 50倍。(相比之下,在先前电子显微镜研究中使用的饱和模板条件下,会激活一种异常的转录模式,这种模式不受rDNA增强子或普遍认可的rDNA启动子的影响)。结果发现,无增强子基因上的活性转录单位与含增强子基因以及内源性rRNA基因上的活性转录单位一样,都密集地充满了新生转录本和聚合酶。值得注意的是,含增强子基因形成这种活性转录单位的可能性比无增强子基因大约高30 - 50倍,这与其转录本数量一致。补充研究证实,增强子不会影响延伸速率、转录复合物的稳定性或转录本半衰期。这些数据表明,后生动物重复rDNA增强子会使更多基因被积极转录,并且不会改变单个活性基因上的重新起始速率。