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布氏锥虫二号染色体的序列及分析

The sequence and analysis of Trypanosoma brucei chromosome II.

作者信息

El-Sayed Najib M A, Ghedin Elodie, Song Jinming, MacLeod Annette, Bringaud Frederic, Larkin Christopher, Wanless David, Peterson Jeremy, Hou Lihua, Taylor Sonya, Tweedie Alison, Biteau Nicolas, Khalak Hanif G, Lin Xiaoying, Mason Tanya, Hannick Linda, Caler Elisabet, Blandin Gaëlle, Bartholomeu Daniella, Simpson Anjana J, Kaul Samir, Zhao Hong, Pai Grace, Van Aken Susan, Utterback Teresa, Haas Brian, Koo Hean L, Umayam Lowell, Suh Bernard, Gerrard Caroline, Leech Vanessa, Qi Rong, Zhou Shiguo, Schwartz David, Feldblyum Tamara, Salzberg Steven, Tait Andrew, Turner C Michael R, Ullu Elisabetta, White Owen, Melville Sara, Adams Mark D, Fraser Claire M, Donelson John E

机构信息

The Institute for Genomic Research, Rockville, MD 20850, USA.

出版信息

Nucleic Acids Res. 2003 Aug 15;31(16):4856-63. doi: 10.1093/nar/gkg673.

Abstract

We report here the sequence of chromosome II from Trypanosoma brucei, the causative agent of African sleeping sickness. The 1.2-Mb pairs encode about 470 predicted genes organised in 17 directional clusters on either strand, the largest cluster of which has 92 genes lined up over a 284-kb region. An analysis of the GC skew reveals strand compositional asymmetries that coincide with the distribution of protein-coding genes, suggesting these asymmetries may be the result of transcription-coupled repair on coding versus non-coding strand. A 5-cM genetic map of the chromosome reveals recombinational 'hot' and 'cold' regions, the latter of which is predicted to include the putative centromere. One end of the chromosome consists of a 250-kb region almost exclusively composed of RHS (pseudo)genes that belong to a newly characterised multigene family containing a hot spot of insertion for retroelements. Interspersed with the RHS genes are a few copies of truncated RNA polymerase pseudogenes as well as expression site associated (pseudo)genes (ESAGs) 3 and 4, and 76 bp repeats. These features are reminiscent of a vestigial variant surface glycoprotein (VSG) gene expression site. The other end of the chromosome contains a 30-kb array of VSG genes, the majority of which are pseudogenes, suggesting that this region may be a site for modular de novo construction of VSG gene diversity during transposition/gene conversion events.

摘要

我们在此报告布氏锥虫(非洲昏睡病的病原体)二号染色体的序列。这120万个碱基对编码约470个预测基因,这些基因在两条链上以17个方向簇的形式排列,其中最大的簇在28.4 kb的区域内排列着92个基因。对GC偏斜的分析揭示了与蛋白质编码基因分布一致的链组成不对称性,这表明这些不对称性可能是编码链与非编码链上转录偶联修复的结果。该染色体的5厘摩遗传图谱揭示了重组的“热点”和“冷点”区域,预计后者包括推定的着丝粒。染色体的一端由一个250 kb的区域组成,该区域几乎完全由RHS(假)基因组成,这些基因属于一个新鉴定的多基因家族,该家族含有反转录元件的插入热点。在RHS基因之间散布着一些截短的RNA聚合酶假基因以及表达位点相关(假)基因(ESAGs)3和4,还有76 bp的重复序列。这些特征让人联想到一个残留的变异表面糖蛋白(VSG)基因表达位点。染色体的另一端包含一个30 kb的VSG基因阵列,其中大多数是假基因,这表明该区域可能是转座/基因转换事件期间VSG基因多样性模块化从头构建的位点。

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