The Genome of the Kinetoplastid Parasite, Leishmania major

Leishmania species cause a spectrum of human diseases in tropical and subtropical regions of the world. We have sequenced the 36 chromosomes of the 32.8-megabase haploid genome of Leishmania major (Friedlin strain) and predict 911 RNA genes, 39 pseudogenes, and 8272 protein-coding genes, of which 36...

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Published inScience (American Association for the Advancement of Science) Vol. 309; no. 5733; pp. 436 - 442
Main Authors Ivens, Alasdair C., Peacock, Christopher S., Worthey, Elizabeth A., Murphy, Lee, Aggarwal, Gautam, Berriman, Matthew, Sisk, Ellen, Rajandream, Marie-Adele, Adlem, Ellen, Aert, Rita, Anupama, Atashi, Apostolou, Zina, Bason, Nathalie, Bauser, Christopher, Beck, Alfred, Beverley, Stephen M., Bianchettin, Gabriella, Borzym, Katja, Bothe, Gordana, Bruschi, Carlo V., Collins, Matt, Cadag, Eithon, Ciarloni, Laura, Clayton, Christine, Richard M. R. Coulson, Cronin, Ann, Cruz, Angela K., Davies, Robert M., De Gaudenzi, Javier, Dobson, Deborah E., Duesterhoeft, Andreas, Fazelina, Gholam, Fosker, Nigel, Frasch, Alberto Carlos, Fraser, Audrey, Fuchs, Monika, Gabel, Claudia, Goble, Arlette, Goffeau, André, Harris, David, Hertz-Fowler, Christiane, Hilbert, Helmut, Horn, David, Huang, Yiting, Klages, Sven, Knights, Andrew, Kube, Michael, Larke, Natasha, Litvin, Lyudmila, Lord, Angela, Louie, Tin, Marra, Marco, Masuy, David, Matthews, Keith, Michaeli, Shulamit, Mottram, Jeremy C., Müller-Auer, Silke, Munden, Heather, Nelson, Siri, Norbertczak, Halina, Oliver, Karen, O'Neil, Susan, Pentony, Martin, Pohl, Thomas M., Price, Claire, Purnelle, Bénédicte, Quail, Michael A., Rabbinowitsch, Ester, Reinhardt, Richard, Rieger, Michael, Rinta, Joel, Robben, Johan, Robertson, Laura, Ruiz, Jeronimo C., Rutter, Simon, Saunders, David, Schäfer, Melanie, Schein, Jacquie, Schwartz, David C., Seeger, Kathy, Seyler, Amber, Sharp, Sarah, Shin, Heesun, Sivam, Dhileep, Squares, Rob, Squares, Steve, Tosato, Valentina, Vogt, Christy, Volckaert, Guido, Wambutt, Rolf, Warren, Tim, Wedler, Holger, Woodward, John, Zhou, Shiguo, Zimmermann, Wolfgang, Smith, Deborah F., Blackwell, Jenefer M., Stuart, Kenneth D., Barrell, Bart, Myler, Peter J.
Format Journal Article
LanguageEnglish
Published United States American Association for the Advancement of Science 15.07.2005
The American Association for the Advancement of Science
Subjects
Online AccessGet full text
ISSN0036-8075
1095-9203
1095-9203
DOI10.1126/science.1112680

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Abstract Leishmania species cause a spectrum of human diseases in tropical and subtropical regions of the world. We have sequenced the 36 chromosomes of the 32.8-megabase haploid genome of Leishmania major (Friedlin strain) and predict 911 RNA genes, 39 pseudogenes, and 8272 protein-coding genes, of which 36% can be ascribed a putative function. These include genes involved in host-pathogen interactions, such as proteolytic enzymes, and extensive machinery for synthesis of complex surface glycoconjugates. The organization of protein-coding genes into long, strand-specific, polycistronic clusters and lack of general transcription factors in the L. major, Trypanosoma brucei, and Trypanosoma cruzi (Tritryp) genomes suggest that the mechanisms regulating RNA polymerase II-directed transcription are distinct from those operating in other eukaryotes, although the trypanosomatids appear capable of chromatin remodeling. Abundant RNA-binding proteins are encoded in the Tritryp genomes, consistent with active posttranscriptional regulation of gene expression.
AbstractList Leishmania species cause a spectrum of human diseases in tropical and subtropical regions of the world. We have sequenced the 36 chromosomes of the 32.8-megabase haploid genome of Leishmania major (Friedlin strain) and predict 911 RNA genes, 39 pseudogenes, and 8272 protein-coding genes, of which 36% can be ascribed a putative function. These include genes involved in host-pathogen interactions, such as proteolytic enzymes, and extensive machinery for synthesis of complex surface glycoconjugates. The organization of protein-coding genes into long, strand-specific, polycistronic clusters and lack of general transcription factors in the L. major, Trypanosoma brucei, and Trypanosoma cruzi (Tritryp) genomes suggest that the mechanisms regulating RNA polymerase II-directed transcription are distinct from those operating in other eukaryotes, although the trypanosomatids appear capable of chromatin remodeling. Abundant RNA-binding proteins are encoded in the Tritryp genomes, consistent with active posttranscriptional regulation of gene expression.
Leishmania species cause a spectrum of human diseases in tropical and subtropical regions of the world. We have sequenced the 36 chromosomes of the 32.8-megabase haploid genome of Leishmania major (Friedlin strain) and predict 911 RNA genes, 39 pseudogenes, and 8272 protein-coding genes, of which 36% can be ascribed a putative function. These include genes involved in host-pathogen interactions, such as proteolytic enzymes, and extensive machinery for synthesis of complex surface glycoconjugates. The organization of protein-coding genes into long, strand-specific, polycistronic clusters and lack of general transcription factors in the L. major, Trypanosoma brucei, and Trypanosoma cruzi (Tritryp) genomes suggest that the mechanisms regulating RNA polymerase II-directed transcription are distinct from those operating in other eukaryotes, although the trypanosomatids appear capable of chromatin remodeling. Abundant RNA-binding proteins are encoded in the Tritryp genomes, consistent with active posttranscriptional regulation of gene expression.Leishmania species cause a spectrum of human diseases in tropical and subtropical regions of the world. We have sequenced the 36 chromosomes of the 32.8-megabase haploid genome of Leishmania major (Friedlin strain) and predict 911 RNA genes, 39 pseudogenes, and 8272 protein-coding genes, of which 36% can be ascribed a putative function. These include genes involved in host-pathogen interactions, such as proteolytic enzymes, and extensive machinery for synthesis of complex surface glycoconjugates. The organization of protein-coding genes into long, strand-specific, polycistronic clusters and lack of general transcription factors in the L. major, Trypanosoma brucei, and Trypanosoma cruzi (Tritryp) genomes suggest that the mechanisms regulating RNA polymerase II-directed transcription are distinct from those operating in other eukaryotes, although the trypanosomatids appear capable of chromatin remodeling. Abundant RNA-binding proteins are encoded in the Tritryp genomes, consistent with active posttranscriptional regulation of gene expression.
Leishmania species cause a spectrum of human diseases in tropical and subtropical regions of the world. We have sequenced the 36 chromosomes of the 32.8-megabase haploid genome of Leishmania major (Friedlin strain) and predict 911 RNA genes, 39 pseudogenes, and 8272 protein-coding genes, of which 36% can be ascribed a putative function. These include genes involved in host-pathogen interactions, such as proteolytic enzymes, and extensive machinery for synthesis of complex surface glycoconjugates. The organization of protein-coding genes into long, strand-specific, polycistronic clusters and lack of general transcription factors in the L. major, Trypanosoma brucei, and Trypanosoma cruzi (Tritryp) genomes suggest that the mechanisms regulating RNA polymerase II-directed transcription are distinct from those operating in other eukaryotes, although the trypanosomatids appear capable of chromatin remodeling. Abundant RNA-binding proteins are encoded in the Tritryp genomes, consistent with active posttranscriptional regulation of gene expression. [PUBLICATION ABSTRACT]
Leishmania species cause a spectrum of human diseases in tropical and subtropical regions of the world. We have sequenced the 36 chromosomes of the 32.8-megabase haploid genome of Leishmania major (Friedlin strain) and predict 911 RNA genes, 39 pseudogenes, and 8272 protein-coding genes, of which 36% can be ascribed a putative function. These include genes involved in host-pathogen interactions, such as proteolytic enzymes, and extensive machinery for synthesis of complex surface glycoconjugates. The organization of protein-coding genes into long, strand-specific, polycistronic clusters and lack of general transcription factors in the L. major, Trypanosoma brucei , and Trypanosoma cruzi (Tritryp) genomes suggest that the mechanisms regulating RNA polymerase II–directed transcription are distinct from those operating in other eukaryotes, although the trypanosomatids appear capable of chromatin remodeling. Abundant RNA-binding proteins are encoded in the Tritryp genomes, consistent with active posttranscriptional regulation of gene expression.
Audience Academic
Author Rabbinowitsch, Ester
Bothe, Gordana
Peacock, Christopher S.
Murphy, Lee
Attipoe, Philip
Bianchettin, Gabriella
Wambutt, Rolf
Reinhardt, Richard
Gabel, Claudia
Schein, Jacquie
Ciarloni, Laura
Horn, David
Beck, Alfred
Munden, Heather
Robertson, Laura
Shin, Heesun
Price, Claire
Müller-Auer, Silke
Knights, Andrew
Stuart, Kenneth D.
Duesterhoeft, Andreas
Huang, Yiting
Ivens, Alasdair C.
Masuy, David
De Gaudenzi, Javier
Borzym, Katja
Aert, Rita
Litvin, Lyudmila
Squares, Rob
Fosker, Nigel
Michaeli, Shulamit
Robben, Johan
Quail, Michael A.
Davies, Robert M.
Squares, Steve
Cadag, Eithon
Klages, Sven
Pentony, Martin
Fraser, Audrey
Woodward, John
Anupama, Atashi
Ruiz, Jeronimo C.
Kube, Michael
Pohl, Thomas M.
Richard M. R. Coulson
Worthey, Elizabeth A.
Nelson, Siri
Rieger, Michael
Barrell, Bart
Blackwell, Jenefer M.
Marra, Marco
Smith, Deborah F.
Apostolou, Zina
Collins, Matt
Norbertczak, Halina
Berriman, Matthew
Adlem, Ellen
Rutter, Simon
Volckaert, Guido
Sisk, Ellen
Hilbert, Helmut
Zimmermann, Wolfgang
Rajandream, Marie-Adele
Schwartz, David C.
Cruz, Angela
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/16020728$$D View this record in MEDLINE/PubMed
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To whom correspondence should be addressed. E-mail: alicat@sanger.ac.uk (A.C.I.), peter.myler@sbri.org (P.J.M.)
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Snippet Leishmania species cause a spectrum of human diseases in tropical and subtropical regions of the world. We have sequenced the 36 chromosomes of the...
Leishmania species cause a spectrum of human diseases in tropical and subtropical regions of the world. We have sequenced the 36 chromosomes of the...
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SubjectTerms Algorithms
Animals
chromatin
Chromatin - genetics
Chromatin - metabolism
Chromosomes
Coding
DNA-directed RNA polymerase
Eukaryotic cells
Gene Expression Regulation
Genes
Genes, Protozoan
Genes, rRNA
Genetic aspects
Genetic loci
Genome, Protozoan
Genomes
Genomics
glycoconjugates
Glycoconjugates - biosynthesis
Glycoconjugates - metabolism
haploidy
host-pathogen relationships
human diseases
Infections
Leishmania major
Leishmania major - chemistry
Leishmania major - genetics
Leishmania major - metabolism
Leishmaniasis
Leishmaniasis, Cutaneous - parasitology
Lipid Metabolism
Macrophages
Membrane Proteins - biosynthesis
Membrane Proteins - chemistry
Membrane Proteins - genetics
Membrane Proteins - metabolism
Molecular Sequence Data
Multigene Family
Parasites
Protein Biosynthesis
Protein Processing, Post-Translational
Proteins
proteolysis
Protozoan Proteins - biosynthesis
Protozoan Proteins - chemistry
Protozoan Proteins - genetics
Protozoan Proteins - metabolism
pseudogenes
RNA
RNA polymerase
RNA Processing, Post-Transcriptional
RNA Splicing
RNA, Protozoan - genetics
RNA, Protozoan - metabolism
RNA-binding proteins
Sequence Analysis, DNA
subtropics
transcription (genetics)
transcription factors
Transcription, Genetic
Translation
Trypanosoma brucei
Trypanosoma cruzi
Zinc
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Title The Genome of the Kinetoplastid Parasite, Leishmania major
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