Literature DB >> 16257065

Evolution of non-LTR retrotransposons in the trypanosomatid genomes: Leishmania major has lost the active elements.

Frédéric Bringaud1, Elodie Ghedin, Gaëlle Blandin, Daniella C Bartholomeu, Elisabet Caler, Mariano J Levin, Théo Baltz, Najib M El-Sayed.   

Abstract

The ingi and L1Tc non-LTR retrotransposons--which constitute the ingi clade--are abundant in the genome of the trypanosomatid species Trypanosoma brucei and Trypanosoma cruzi, respectively. The corresponding retroelements, however, are not present in the genome of a closely related trypanosomatid, Leishmania major. To study the evolution of non-LTR retrotransposons in trypanosomatids, we have analyzed all ingi/L1Tc elements and highly degenerate ingi/L1Tc-related sequences identified in the recently completed T. brucei, T. cruzi and L. major genomes. The coding sequences of 242 degenerate ingi/L1Tc-related elements (DIREs) in all three genomes were reconstituted by removing the numerous frame shifts. Three independent phylogenetic analyses conducted on the conserved domains encoded by these elements show that all DIREs, including the 52 L. major DIREs, form a monophyletic group belonging to the ingi clade. This indicates that the trypanosomatid ancestor contained active mobile elements that have been retained in the Trypanosoma species, but were lost from L. major genome, where only remnants (DIRE) are detectable. All 242 DIREs analyzed group together according to their species origin with the exception of 11 T. cruzi DIREs which are close to the T. brucei ingi/DIRE families. Considering the absence of known horizontal transfer between the African T. brucei and the South-American T. cruzi, this suggests that this group of elements evolved at a lower rate when compared to the other trypanosomatid elements. Interestingly, the only nucleotide sequence conserved between ingi and L1Tc (the first 79 residues) is also present at the 5'-extremity of all the full length DIREs and suggests a possible role for this conserved motif, as well as for DIREs.

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Year:  2005        PMID: 16257065     DOI: 10.1016/j.molbiopara.2005.09.017

Source DB:  PubMed          Journal:  Mol Biochem Parasitol        ISSN: 0166-6851            Impact factor:   1.759


  20 in total

1.  Trypanosomatid genomes contain several subfamilies of ingi-related retroposons.

Authors:  Frédéric Bringaud; Matthew Berriman; Christiane Hertz-Fowler
Journal:  Eukaryot Cell       Date:  2009-08-07

2.  Identification of the centromeres of Leishmania major: revealing the hidden pieces.

Authors:  Maria-Rosa Garcia-Silva; Lauriane Sollelis; Cameron Ross MacPherson; Slavica Stanojcic; Nada Kuk; Lucien Crobu; Frédéric Bringaud; Patrick Bastien; Michel Pagès; Artur Scherf; Yvon Sterkers
Journal:  EMBO Rep       Date:  2017-09-21       Impact factor: 8.807

3.  TBP and SNAP50 transcription factors bind specifically to the Pr77 promoter sequence from trypanosomatid non-LTR retrotransposons.

Authors:  Francisco Macías; Raquel Afonso-Lehmann; Patricia E Carreira; M Carmen Thomas
Journal:  Parasit Vectors       Date:  2021-06-09       Impact factor: 3.876

4.  Centromere-associated topoisomerase activity in bloodstream form Trypanosoma brucei.

Authors:  Samson O Obado; Christopher Bot; Maria C Echeverry; Julio C Bayona; Vanina E Alvarez; Martin C Taylor; John M Kelly
Journal:  Nucleic Acids Res       Date:  2010-09-22       Impact factor: 16.971

5.  Rapid decay of unstable Leishmania mRNAs bearing a conserved retroposon signature 3'-UTR motif is initiated by a site-specific endonucleolytic cleavage without prior deadenylation.

Authors:  Michaela Müller; Prasad K Padmanabhan; Annie Rochette; Debdutta Mukherjee; Martin Smith; Carole Dumas; Barbara Papadopoulou
Journal:  Nucleic Acids Res       Date:  2010-05-07       Impact factor: 16.971

6.  Pr77 and L1TcRz: A dual system within the 5'-end of L1Tc retrotransposon, internal promoter and HDV-like ribozyme.

Authors:  Francisco Sánchez-Luque; Manuel C López; Francisco Macias; Carlos Alonso; M Carmen Thomas
Journal:  Mob Genet Elements       Date:  2012-01-01

7.  Organization and evolution of two SIDER retroposon subfamilies and their impact on the Leishmania genome.

Authors:  Martin Smith; Frédéric Bringaud; Barbara Papadopoulou
Journal:  BMC Genomics       Date:  2009-05-22       Impact factor: 3.969

8.  Comparative genomic analysis of three Leishmania species that cause diverse human disease.

Authors:  Christopher S Peacock; Kathy Seeger; David Harris; Lee Murphy; Jeronimo C Ruiz; Michael A Quail; Nick Peters; Ellen Adlem; Adrian Tivey; Martin Aslett; Arnaud Kerhornou; Alasdair Ivens; Audrey Fraser; Marie-Adele Rajandream; Tim Carver; Halina Norbertczak; Tracey Chillingworth; Zahra Hance; Kay Jagels; Sharon Moule; Doug Ormond; Simon Rutter; Rob Squares; Sally Whitehead; Ester Rabbinowitsch; Claire Arrowsmith; Brian White; Scott Thurston; Frédéric Bringaud; Sandra L Baldauf; Adam Faulconbridge; Daniel Jeffares; Daniel P Depledge; Samuel O Oyola; James D Hilley; Loislene O Brito; Luiz R O Tosi; Barclay Barrell; Angela K Cruz; Jeremy C Mottram; Deborah F Smith; Matthew Berriman
Journal:  Nat Genet       Date:  2007-06-17       Impact factor: 38.330

Review 9.  Comparative genomics: from genotype to disease phenotype in the leishmaniases.

Authors:  Deborah F Smith; Christopher S Peacock; Angela K Cruz
Journal:  Int J Parasitol       Date:  2007-06-23       Impact factor: 3.981

10.  The L1Tc non-LTR retrotransposon of Trypanosoma cruzi contains an internal RNA-pol II-dependent promoter that strongly activates gene transcription and generates unspliced transcripts.

Authors:  Sara R Heras; Manuel C López; Mónica Olivares; M Carmen Thomas
Journal:  Nucleic Acids Res       Date:  2007-03-16       Impact factor: 16.971

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