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动质体寄生原生动物中的端粒酶。

Telomerase in kinetoplastid parasitic protozoa.

作者信息

Cano M I, Dungan J M, Agabian N, Blackburn E H

机构信息

Department of Microbiology and Immunology, University of California, San Francisco, CA 94123, USA.

出版信息

Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):3616-21. doi: 10.1073/pnas.96.7.3616.

Abstract

We have identified telomerase activity in extracts of three evolutionarily diverse kinetoplastid species: Trypanosoma brucei, Leishmania major, and Leishmania tarentolae. Telomerase activity was initially detected in extracts from insect form cells of all three kinetoplastid species by using a modification of the one-tube telomere repeat amplification protocol [Kim, N., et al. (1994) Science 266, 2011-2015], although better results were subsequently achieved with the two-tube telomere repeat amplification protocol [Autexier, C., Pruzan, R., Funk, W. & Greider, C. (1996) EMBO J. 15, 5928-5935]. The activity in T. brucei extracts was sufficiently robust to enable its detection in a direct assay of telomerase; enzyme processivity was found to be relatively low. The in vitro properties of telomerase suggest a possible templating domain sequence for the telomerase RNA of T. brucei. Telomerase activity is likely to contribute to telomere maintenance in these parasitic organisms and provides a new target for chemotherapeutic intervention.

摘要

我们在三种进化上不同的动基体目物种的提取物中鉴定出了端粒酶活性

布氏锥虫、硕大利什曼原虫和热带利什曼原虫。通过对单管端粒重复序列扩增方案进行改进 [金,N. 等人(1994年)《科学》266,2011 - 2015页],最初在所有这三种动基体目物种的昆虫形态细胞提取物中检测到了端粒酶活性,不过随后使用双管端粒重复序列扩增方案 [奥泰西尔,C.,普鲁赞,R.,芬克,W. & 格雷德,C.(1996年)《欧洲分子生物学组织杂志》15,5928 - 5935页] 取得了更好的结果。布氏锥虫提取物中的活性足够强,能够在端粒酶的直接检测中被发现;发现酶的持续合成能力相对较低。端粒酶的体外特性表明了布氏锥虫端粒酶RNA可能的模板结构域序列。端粒酶活性可能有助于这些寄生生物中端粒的维持,并为化疗干预提供了一个新靶点。

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Telomerase in kinetoplastid parasitic protozoa.动质体寄生原生动物中的端粒酶。
Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):3616-21. doi: 10.1073/pnas.96.7.3616.

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