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酵母 Saccharomyces cerevisiae 的端粒酶复合物含有一个生物素化的成分。

Telomerase Complex from Yeast Saccharomyces cerevisiae Contains a Biotinylated Component.

机构信息

Department of Chemistry, Moscow State University.

出版信息

Acta Naturae. 2009 Jul;1(2):81-5.

PMID:22649607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3347513/
Abstract

Telomerase adds telomeric repeats to single-stranded DNA at the ends of the chromosomes. This enzyme is a ribonucleoprotein complex. Telomerase from yeast Saccharomyces cerevisiae consists of TLC1 RNA, which serves as a template for the synthesis of telomeric repeats, telomerase reverse transcriptase Est2p, and a number of accessory proteins (Est1p, Est3p, Ku70/Ku80, and Sm-complex). We found that the yeast telomerase complex contains a biotinylated component. The telomerase fraction containing biotinylated protein is active in vitro and constitutes a small part of the total amount of active telomerase isolated from cells. We speculate about the nature of the biotinylated component.

摘要

端粒酶将端粒重复序列添加到染色体末端的单链 DNA 上。这种酶是一种核糖核蛋白复合物。来自酿酒酵母的端粒酶由 TLC1 RNA 组成,它作为端粒重复序列合成的模板,端粒酶逆转录酶 Est2p 和许多辅助蛋白(Est1p、Est3p、Ku70/Ku80 和 Sm 复合物)。我们发现酵母端粒酶复合物含有一个生物素化的成分。含有生物素化蛋白的端粒酶部分在体外具有活性,并且构成从细胞中分离的总活性端粒酶的一小部分。我们推测生物素化成分的性质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f3/3347513/5401cca7dfed/AN20758251-02-081-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f3/3347513/edc2b2162e16/AN20758251-02-081-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f3/3347513/636b57c091ba/AN20758251-02-081-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f3/3347513/ed6fc188dd20/AN20758251-02-081-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f3/3347513/5401cca7dfed/AN20758251-02-081-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f3/3347513/edc2b2162e16/AN20758251-02-081-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f3/3347513/636b57c091ba/AN20758251-02-081-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f3/3347513/ed6fc188dd20/AN20758251-02-081-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f3/3347513/5401cca7dfed/AN20758251-02-081-g004.jpg

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1
Telomerase Complex from Yeast Saccharomyces cerevisiae Contains a Biotinylated Component.酵母 Saccharomyces cerevisiae 的端粒酶复合物含有一个生物素化的成分。
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本文引用的文献

1
A genome-wide screen for essential yeast genes that affect telomere length maintenance.一项针对影响端粒长度维持的酵母必需基因的全基因组筛选。
Nucleic Acids Res. 2009 Jul;37(12):3840-9. doi: 10.1093/nar/gkp259. Epub 2009 Apr 22.
2
The hsp90 molecular chaperone modulates multiple telomerase activities.热休克蛋白90(Hsp90)分子伴侣调节多种端粒酶活性。
Mol Cell Biol. 2008 Jan;28(1):457-67. doi: 10.1128/MCB.01417-07. Epub 2007 Oct 22.
3
Telomerase repeat addition processivity is increased at critically short telomeres in a Tel1-dependent manner in Saccharomyces cerevisiae.
在酿酒酵母中,端粒酶重复序列添加的持续性以依赖于Tel1的方式在极短的端粒处增加。
Genes Dev. 2007 Oct 1;21(19):2485-94. doi: 10.1101/gad.1588807.
4
Tel1p preferentially associates with short telomeres to stimulate their elongation.端粒酶1优先与短端粒结合以刺激其延长。
Mol Cell. 2007 Sep 7;27(5):851-8. doi: 10.1016/j.molcel.2007.08.007.
5
Telomerase and Tel1p preferentially associate with short telomeres in S. cerevisiae.端粒酶和Tel1p在酿酒酵母中优先与短端粒结合。
Mol Cell. 2007 Aug 17;27(4):550-61. doi: 10.1016/j.molcel.2007.07.016. Epub 2007 Jul 26.
6
Low abundance of telomerase in yeast: implications for telomerase haploinsufficiency.酵母中端粒酶丰度较低:对端粒酶单倍剂量不足的影响。
RNA. 2006 Sep;12(9):1721-37. doi: 10.1261/rna.134706. Epub 2006 Aug 7.
7
Proteasome-dependent degradation of Est1p regulates the cell cycle-restricted assembly of telomerase in Saccharomyces cerevisiae.蛋白酶体依赖性的Est1p降解调控酿酒酵母中端粒酶的细胞周期限制组装。
Nat Struct Mol Biol. 2006 Aug;13(8):720-8. doi: 10.1038/nsmb1125. Epub 2006 Jul 23.
8
The biogenesis and regulation of telomerase holoenzymes.端粒酶全酶的生物合成与调控
Nat Rev Mol Cell Biol. 2006 Jul;7(7):484-94. doi: 10.1038/nrm1961.
9
Cell cycle-dependent regulation of yeast telomerase by Ku.Ku对酵母端粒酶的细胞周期依赖性调控。
Nat Struct Mol Biol. 2004 Dec;11(12):1198-205. doi: 10.1038/nsmb854. Epub 2004 Nov 7.
10
Purification of biotinylated proteins on streptavidin resin: a protocol for quantitative elution.利用链霉亲和素树脂纯化生物素化蛋白:定量洗脱方案
Proteomics. 2004 Aug;4(8):2296-9. doi: 10.1002/pmic.200300780.