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相似文献

1
Specific telomerase RNA residues distant from the template are essential for telomerase function.远离模板的特定端粒酶RNA残基对于端粒酶功能至关重要。
Genes Dev. 1998 Oct 15;12(20):3286-300. doi: 10.1101/gad.12.20.3286.
2
The 5' arm of Kluyveromyces lactis telomerase RNA is critical for telomerase function.乳酸克鲁维酵母端粒酶RNA的5'臂对端粒酶功能至关重要。
Mol Cell Biol. 2008 Mar;28(6):1875-82. doi: 10.1128/MCB.01683-07. Epub 2008 Jan 14.
3
Identification of Kluyveromyces lactis telomerase: discontinuous synthesis along the 30-nucleotide-long templating domain.乳酸克鲁维酵母端粒酶的鉴定:沿30个核苷酸长的模板结构域的不连续合成。
Mol Cell Biol. 1998 Sep;18(9):4961-70. doi: 10.1128/MCB.18.9.4961.
4
Template boundary in a yeast telomerase specified by RNA structure.由RNA结构指定的酵母端粒酶中的模板边界。
Science. 2000 May 5;288(5467):863-7. doi: 10.1126/science.288.5467.863.
5
Pyrimidine motif triple helix in the Kluyveromyces lactis telomerase RNA pseudoknot is essential for function in vivo.酿酒酵母端粒酶 RNA 发夹结构中的嘧啶基三联体三螺旋对于体内功能至关重要。
Proc Natl Acad Sci U S A. 2013 Jul 2;110(27):10970-5. doi: 10.1073/pnas.1309590110. Epub 2013 Jun 17.
6
Altering specific telomerase RNA template residues affects active site function.改变特定的端粒酶RNA模板残基会影响活性位点功能。
Genes Dev. 1995 Sep 15;9(18):2214-26. doi: 10.1101/gad.9.18.2214.
7
A critical three-way junction is conserved in budding yeast and vertebrate telomerase RNAs.一个关键的三向连接在出芽酵母和脊椎动物端粒酶RNA中保守存在。
Nucleic Acids Res. 2007;35(18):6280-9. doi: 10.1093/nar/gkm713. Epub 2007 Sep 13.
8
Telomerase RNA mutations in Saccharomyces cerevisiae alter telomerase action and reveal nonprocessivity in vivo and in vitro.酿酒酵母中的端粒酶RNA突变改变端粒酶作用,并揭示体内和体外的非持续性。
Genes Dev. 1997 Feb 15;11(4):528-40. doi: 10.1101/gad.11.4.528.
9
An enhanced H/ACA RNP assembly mechanism for human telomerase RNA.人端粒酶 RNA 的增强 H/ACA RNP 组装机制。
Mol Cell Biol. 2012 Jul;32(13):2428-39. doi: 10.1128/MCB.00286-12. Epub 2012 Apr 23.
10
Template requirements for telomerase translocation in Kluyveromyces lactis.乳酸克鲁维酵母中端粒酶易位的模板要求。
Mol Cell Biol. 2004 Jan;24(2):912-23. doi: 10.1128/MCB.24.2.912-923.2004.

引用本文的文献

1
Functional Interactions of Telomerase Reverse Transcriptase with the Three-Way Junction and the Template Domains of Telomerase RNA.端粒酶逆转录酶与端粒酶 RNA 的三链结和模板结构域的功能相互作用。
Int J Mol Sci. 2022 Sep 15;23(18):10757. doi: 10.3390/ijms231810757.
2
Telomerase, the recombination machinery and Rap1 play redundant roles in yeast telomere protection.端粒酶、重组机制和 Rap1 在酵母端粒保护中发挥冗余作用。
Curr Genet. 2021 Feb;67(1):153-163. doi: 10.1007/s00294-020-01125-4. Epub 2020 Nov 6.
3
Pyrimidine motif triple helix in the Kluyveromyces lactis telomerase RNA pseudoknot is essential for function in vivo.酿酒酵母端粒酶 RNA 发夹结构中的嘧啶基三联体三螺旋对于体内功能至关重要。
Proc Natl Acad Sci U S A. 2013 Jul 2;110(27):10970-5. doi: 10.1073/pnas.1309590110. Epub 2013 Jun 17.
4
Long telomeres produced by telomerase-resistant recombination are established from a single source and are subject to extreme sequence scrambling.由端粒酶抗性重组产生的长端粒是由单一来源产生的,并受到极端序列混乱的影响。
PLoS Genet. 2012;8(11):e1003017. doi: 10.1371/journal.pgen.1003017. Epub 2012 Nov 1.
5
"Poisoning" yeast telomeres distinguishes between redundant telomere capping pathways.“毒害”酵母端粒可区分冗余的端粒封端途径。
Chromosoma. 2012 Dec;121(6):613-27. doi: 10.1007/s00412-012-0385-6. Epub 2012 Oct 6.
6
Maintenance of very long telomeres by recombination in the Kluyveromyces lactis stn1-M1 mutant involves extreme telomeric turnover, telomeric circles, and concerted telomeric amplification.在 Kluyveromyces lactis stn1-M1 突变体中,通过重组维持非常长的端粒涉及极端端粒翻转、端粒环和协调的端粒扩增。
Mol Cell Biol. 2012 Aug;32(15):2992-3008. doi: 10.1128/MCB.00430-12. Epub 2012 May 29.
7
Recombination can either help maintain very short telomeres or generate longer telomeres in yeast cells with weak telomerase activity.在端粒酶活性较弱的酵母细胞中,重组作用既可以帮助维持非常短的端粒,也可以产生更长的端粒。
Eukaryot Cell. 2011 Aug;10(8):1131-42. doi: 10.1128/EC.05079-11. Epub 2011 Jun 10.
8
Recombination can cause telomere elongations as well as truncations deep within telomeres in wild-type Kluyveromyces lactis cells.在野生型乳酸克鲁维酵母细胞中,重组可导致端粒延长以及端粒内部深处的截短。
Eukaryot Cell. 2011 Feb;10(2):226-36. doi: 10.1128/EC.00209-10. Epub 2010 Dec 10.
9
Ribonucleoprotein multimers and their functions.核糖核蛋白多聚体及其功能。
Crit Rev Biochem Mol Biol. 2010 Oct;45(5):331-50. doi: 10.3109/10409238.2010.496772.
10
Identification and comparative analysis of telomerase RNAs from Candida species reveal conservation of functional elements.念珠菌属端粒酶RNA的鉴定与比较分析揭示了功能元件的保守性。
RNA. 2009 Apr;15(4):546-59. doi: 10.1261/rna.1194009. Epub 2009 Feb 17.

本文引用的文献

1
Identification of Kluyveromyces lactis telomerase: discontinuous synthesis along the 30-nucleotide-long templating domain.乳酸克鲁维酵母端粒酶的鉴定:沿30个核苷酸长的模板结构域的不连续合成。
Mol Cell Biol. 1998 Sep;18(9):4961-70. doi: 10.1128/MCB.18.9.4961.
2
Interaction of recombinant Tetrahymena telomerase proteins p80 and p95 with telomerase RNA and telomeric DNA substrates.重组四膜虫端粒酶蛋白p80和p95与端粒酶RNA及端粒DNA底物的相互作用。
Genes Dev. 1998 Mar 1;12(5):721-33. doi: 10.1101/gad.12.5.721.
3
Mechanical devices of the spliceosome: motors, clocks, springs, and things.剪接体的机械装置:马达、时钟、弹簧及其他部件。
Cell. 1998 Feb 6;92(3):315-26. doi: 10.1016/s0092-8674(00)80925-3.
4
Mutational analysis of the Tetrahymena telomerase RNA: identification of residues affecting telomerase activity in vitro.嗜热四膜虫端粒酶RNA的突变分析:体外影响端粒酶活性的残基鉴定
Nucleic Acids Res. 1998 Feb 1;26(3):787-95. doi: 10.1093/nar/26.3.787.
5
Reconstitution of human telomerase activity in vitro.体外重建人端粒酶活性。
Curr Biol. 1998 Jan 29;8(3):177-80. doi: 10.1016/s0960-9822(98)70067-3.
6
Reconstitution of human telomerase with the template RNA component hTR and the catalytic protein subunit hTRT.用人端粒酶模板RNA成分hTR和催化蛋白亚基hTRT重组人端粒酶。
Nat Genet. 1997 Dec;17(4):498-502. doi: 10.1038/ng1297-498.
7
Human telomerase contains evolutionarily conserved catalytic and structural subunits.人类端粒酶包含进化上保守的催化亚基和结构亚基。
Genes Dev. 1997 Dec 1;11(23):3109-15. doi: 10.1101/gad.11.23.3109.
8
Functionally interacting telomerase RNAs in the yeast telomerase complex.酵母端粒酶复合物中功能相互作用的端粒酶RNA
Genes Dev. 1997 Nov 1;11(21):2790-800. doi: 10.1101/gad.11.21.2790.
9
Reprogramming of telomerase by expression of mutant telomerase RNA template in human cells leads to altered telomeres that correlate with reduced cell viability.在人类细胞中通过表达突变的端粒酶RNA模板对端粒酶进行重编程会导致端粒改变,这与细胞活力降低相关。
Mol Cell Biol. 1997 Nov;17(11):6394-401. doi: 10.1128/MCB.17.11.6394.
10
Three Ever Shorter Telomere (EST) genes are dispensable for in vitro yeast telomerase activity.三个端粒不断缩短(EST)基因对于体外酵母端粒酶活性而言并非必需。
Proc Natl Acad Sci U S A. 1997 Oct 14;94(21):11190-5. doi: 10.1073/pnas.94.21.11190.

远离模板的特定端粒酶RNA残基对于端粒酶功能至关重要。

Specific telomerase RNA residues distant from the template are essential for telomerase function.

作者信息

Roy J, Fulton T B, Blackburn E H

机构信息

Departments of Microbiology and Immunology and Biochemistry and Biophysics, University of California, San Francisco, San Francisco, California 94143-0414 USA.

出版信息

Genes Dev. 1998 Oct 15;12(20):3286-300. doi: 10.1101/gad.12.20.3286.

DOI:10.1101/gad.12.20.3286
PMID:9784502
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC317211/
Abstract

The reverse transcriptase telomerase is a ribonucleoprotein complex that adds telomeric repeats to chromosome ends, using a sequence within its endogenous RNA component as a template. Although templating domains of telomerase RNA have been studied in detail, little is known about the roles of the remaining residues, particularly in yeast. We examined the functions of nontemplate telomerase residues in the telomerase RNA of budding yeast Kluyveromyces lactis. Although approximately half of the RNA residues were dispensable for function, four specific regions were essential for telomerase action in vivo. We analyzed the effects of mutating these regions on in vivo function, in vitro telomerase activity, and telomerase RNP assembly. Deletion of two regions resulted in synthesis of stable RNAs that appeared unable to assemble into a stable RNP. Mutating a region near the 5' end of the RNA allowed RNP assembly but abolished enzymatic activity. Mutations in another specific small region of the RNA led to an inactive telomerase RNP with an altered RNA conformation.

摘要

逆转录酶端粒酶是一种核糖核蛋白复合体,它利用其内源性RNA组分中的序列作为模板,将端粒重复序列添加到染色体末端。尽管端粒酶RNA的模板结构域已被详细研究,但对于其余残基的作用却知之甚少,尤其是在酵母中。我们研究了出芽酵母乳酸克鲁维酵母端粒酶RNA中非模板端粒酶残基的功能。尽管约一半的RNA残基对于功能是可有可无的,但有四个特定区域对于体内端粒酶作用至关重要。我们分析了这些区域发生突变对体内功能、体外端粒酶活性和端粒酶核糖核蛋白(RNP)组装的影响。删除两个区域导致合成出稳定的RNA,这些RNA似乎无法组装成稳定的RNP。在RNA 5'端附近的一个区域发生突变允许RNP组装,但消除了酶活性。RNA另一个特定小区域的突变导致产生一种无活性的端粒酶RNP,其RNA构象发生改变。