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布氏锥虫端粒长度变化与抗原变异的关联

Changes in telomere length associated with antigenic variation in Trypanosoma brucei.

作者信息

Myler P J, Aline R F, Scholler J K, Stuart K D

机构信息

Seattle Biomedical Research Institute, WA 98109-1651.

出版信息

Mol Biochem Parasitol. 1988 Jun;29(2-3):243-50. doi: 10.1016/0166-6851(88)90079-5.

DOI:10.1016/0166-6851(88)90079-5
PMID:2842675
Abstract

In the IsTaR 1 serodeme, we have identified variant surface glycoprotein (VSG) genes in nine different telomeric sites. We have measured the distance from the 3' end of these VSG genes to the end of the chromosome (the 'telomere length') in 20 variant antigen types (VATs) of the serodeme. Analyses of the changes in telomere length during 19 antigenic switches involving eight telomeric sites indicate a median increase in telomere length of 0.6 kilobase pairs during each switch. This may be accounted for by the 6-10 bp increase in telomere length per generation associated with DNA replication described by others. The changes in telomere lengths do not form a normal distribution since a substantial fraction show unusually large increases in telomere length or decreases in telomere length during an antigenic switch. These changes are probably caused by recombinations 3' to the VSG gene. No significant differences were detected in the behavior of telomeres at each of the eight different telomeric sites, nor were changes in telomere lengths significantly different between different antigenic switches. However, it was found that those telomeres where transcription was activated during the antigenic switch showed a significantly greater increase in telomere length than those telomeres not involved in regulation of VSG gene expression. Conversely, there was a strong correlation between transcriptional inactivation of a telomeric expression site and a decrease in telomere length. These findings suggest that processes (possibly genomic recombinations) 3' to the VSG gene coding region may be associated with a change in the transcriptional status of the VSG gene.

摘要

在IsTaR 1血清型中,我们在9个不同的端粒位点鉴定出了变异表面糖蛋白(VSG)基因。我们测量了该血清型20种变异抗原类型(VATs)中这些VSG基因3'端到染色体末端的距离(“端粒长度”)。对涉及8个端粒位点的19次抗原转换过程中端粒长度变化的分析表明,每次转换过程中端粒长度的中位数增加为0.6千碱基对。这可能是由其他人描述的与DNA复制相关的每代端粒长度增加6 - 10碱基对所导致的。端粒长度变化并不呈正态分布,因为在抗原转换过程中,相当一部分端粒长度显示出异常大幅的增加或减少。这些变化可能是由VSG基因3'端的重组引起的。在8个不同端粒位点的端粒行为中未检测到显著差异,不同抗原转换之间的端粒长度变化也没有显著差异。然而,发现那些在抗原转换过程中转录被激活的端粒,其端粒长度的增加显著大于那些不参与VSG基因表达调控的端粒。相反,端粒表达位点的转录失活与端粒长度的减少之间存在很强的相关性。这些发现表明,VSG基因编码区3'端的过程(可能是基因组重组)可能与VSG基因转录状态的变化有关。

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Changes in telomere length associated with antigenic variation in Trypanosoma brucei.布氏锥虫端粒长度变化与抗原变异的关联
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The two mechanisms for antigenic variation in Trypanosoma brucei are independent processes.布氏锥虫抗原变异的两种机制是独立的过程。
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Telomere length affects the frequency and mechanism of antigenic variation in Trypanosoma brucei.端粒长度影响布氏锥虫抗原变异的频率和机制。
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Telomere exchange can be an important mechanism of variant surface glycoprotein gene switching in Trypanosoma brucei.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。
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Escaping the immune system by DNA repair and recombination in African trypanosomes.通过 DNA 修复和重组逃避非洲锥虫的免疫系统。
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Chromosome ends as adaptive beginnings: the potential role of dysfunctional telomeres in subtelomeric evolvability.
作为适应性开端的染色体末端:功能失调的端粒在亚端粒可进化性中的潜在作用。
Curr Genet. 2018 Oct;64(5):997-1000. doi: 10.1007/s00294-018-0822-z. Epub 2018 Mar 27.
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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.
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Consequences of telomere shortening at an active VSG expression site in telomerase-deficient Trypanosoma brucei.端粒酶缺陷型布氏锥虫中活性VSG表达位点处端粒缩短的后果。
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