Literature DB >> 12907728

The sequence and analysis of Trypanosoma brucei chromosome II.

Najib M A El-Sayed1, Elodie Ghedin, Jinming Song, Annette MacLeod, Frederic Bringaud, Christopher Larkin, David Wanless, Jeremy Peterson, Lihua Hou, Sonya Taylor, Alison Tweedie, Nicolas Biteau, Hanif G Khalak, Xiaoying Lin, Tanya Mason, Linda Hannick, Elisabet Caler, Gaëlle Blandin, Daniella Bartholomeu, Anjana J Simpson, Samir Kaul, Hong Zhao, Grace Pai, Susan Van Aken, Teresa Utterback, Brian Haas, Hean L Koo, Lowell Umayam, Bernard Suh, Caroline Gerrard, Vanessa Leech, Rong Qi, Shiguo Zhou, David Schwartz, Tamara Feldblyum, Steven Salzberg, Andrew Tait, C Michael R Turner, Elisabetta Ullu, Owen White, Sara Melville, Mark D Adams, Claire M Fraser, John E Donelson.   

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.

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Year:  2003        PMID: 12907728      PMCID: PMC169936          DOI: 10.1093/nar/gkg673

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  46 in total

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10.  The molecular karyotype of the megabase chromosomes of Trypanosoma brucei and the assignment of chromosome markers.

Authors:  S E Melville; V Leech; C S Gerrard; A Tait; J M Blackwell
Journal:  Mol Biochem Parasitol       Date:  1998-08-01       Impact factor: 1.759

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  19 in total

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3.  A novel strategy to identify the location of necessary and sufficient cis-acting regulatory mRNA elements in trypanosomes.

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4.  Small trypanosome RNA-binding proteins TbUBP1 and TbUBP2 influence expression of F-box protein mRNAs in bloodstream trypanosomes.

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Journal:  Eukaryot Cell       Date:  2007-09-14

5.  Advancing Trypanosoma brucei genome annotation through ribosome profiling and spliced leader mapping.

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Review 6.  Telomere and Subtelomere R-loops and Antigenic Variation in Trypanosomes.

Authors:  Arpita Saha; Vishal P Nanavaty; Bibo Li
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7.  The genome of the kinetoplastid parasite, Leishmania major.

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8.  Functional characterization of a Trypanosoma brucei TATA-binding protein-related factor points to a universal regulator of transcription in trypanosomes.

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9.  Transposons to toxins: the provenance, architecture and diversification of a widespread class of eukaryotic effectors.

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Journal:  Nucleic Acids Res       Date:  2016-04-08       Impact factor: 16.971

10.  Heat shock causes a decrease in polysomes and the appearance of stress granules in trypanosomes independently of eIF2(alpha) phosphorylation at Thr169.

Authors:  Susanne Kramer; Rafael Queiroz; Louise Ellis; Helena Webb; Jörg D Hoheisel; Christine Clayton; Mark Carrington
Journal:  J Cell Sci       Date:  2008-08-19       Impact factor: 5.285

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