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端粒交换可能是布氏锥虫变异表面糖蛋白基因转换的重要机制。

Telomere exchange can be an important mechanism of variant surface glycoprotein gene switching in Trypanosoma brucei.

作者信息

Rudenko G, McCulloch R, Dirks-Mulder A, Borst P

机构信息

Department of Molecular Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

出版信息

Mol Biochem Parasitol. 1996 Sep;80(1):65-75. doi: 10.1016/0166-6851(96)02669-2.

Abstract

Trypanosoma brucei undergoes antigenic variation by changing its Variant Surface Glycoprotein (VSG) coat. Although there are up to a thousand VSG genes, only one is transcribed at a time from a telomeric VSG expression site. Switching can involve DNA rearrangements exchanging the active VSG gene, or transcriptional activation of a new expression site and transcriptional silencing of the old one. Determining the mechanism mediating a switch has not always been easy, as the many virtually identical copies of VSG gene expression sites complicate transcriptional analysis. To overcome this problem, we have used bloodstream form T. brucei with a single copy VSG gene in an active expression site marked with a hygromycin resistance gene. We allowed these transformants to undergo switching of the active VSG gene, via three different experimental methods. We were able to select large numbers of switched trypanosomes from a single infected mouse using a new microtitre-dish based procedure developed for this purpose. The drug sensitivity of the switched trypanosomes allowed us to determine the transcriptional state of the marked expression site, and polymerase chain reaction (PCR) amplification was used to determine whether the single copy drug resistance gene and VSG gene present in the marked expression site had been retained. These studies showed that telomere exchange, which has been considered rare, can in some cases be an important mechanism of VSG gene switching. We describe 4 telomere exchange events between the active VSG 221 expression site and 4 different chromosomes.

摘要

布氏锥虫通过改变其可变表面糖蛋白(VSG)外壳来进行抗原变异。尽管有多达一千个VSG基因,但在任何时候只有一个从端粒VSG表达位点转录。转换可能涉及DNA重排,交换活性VSG基因,或者新表达位点的转录激活和旧表达位点的转录沉默。确定介导转换的机制并非总是容易的,因为VSG基因表达位点的许多几乎相同的拷贝使转录分析变得复杂。为了克服这个问题,我们使用了在带有潮霉素抗性基因标记的活性表达位点上具有单拷贝VSG基因的血流型布氏锥虫。我们通过三种不同的实验方法让这些转化体进行活性VSG基因的转换。我们能够使用为此目的开发的基于新的微量滴定板的程序从一只感染的小鼠中筛选出大量转换后的锥虫。转换后的锥虫的药物敏感性使我们能够确定标记表达位点的转录状态,并使用聚合酶链反应(PCR)扩增来确定标记表达位点中存在的单拷贝耐药基因和VSG基因是否被保留。这些研究表明,一直被认为罕见的端粒交换在某些情况下可能是VSG基因转换的重要机制。我们描述了活性VSG 221表达位点与4条不同染色体之间的4次端粒交换事件。

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