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1.
PLoS One ; 6(2): e16743, 2011 Feb 10.
Artículo en Inglés | MEDLINE | ID: mdl-21379317

RESUMEN

Horizontal transfer of genetic material between complex organisms often involves transposable elements (TEs). For example, a DNA transposon mariner has been shown to undergo horizontal transfer between different orders of insects and between different phyla of animals. Here we report the discovery and characterization of an ITmD37D transposon, MJ1, in Anopheles sinensis. We show that some MJ1 elements in Aedes aegypti and An. sinensis contain intact open reading frames and share nearly 99% nucleotide identity over the entire transposon, which is unexpectedly high given that these two genera had diverged 145-200 million years ago. Chromosomal hybridization and TE-display showed that MJ1 copy number is low in An. sinensis. Among 24 mosquito species surveyed, MJ1 is only found in Ae. aegypti and the hyrcanus group of anopheline mosquitoes to which An. sinensis belongs. Phylogenetic analysis is consistent with horizontal transfer and provides the basis for inference of its timing and direction. Although report of horizontal transfer of DNA transposons between higher eukaryotes is accumulating, our analysis is one of a small number of cases in which horizontal transfer of nearly identical TEs among highly divergent species has been thoroughly investigated and strongly supported. Horizontal transfer involving mosquitoes is of particular interest because there are ongoing investigations of the possibility of spreading pathogen-resistant genes into mosquito populations to control malaria and other infectious diseases. The initial indication of horizontal transfer of MJ1 came from comparisons between a 0.4x coverage An. sinensis 454 sequence database and available TEs in mosquito genomes. Therefore we have shown that it is feasible to use low coverage sequencing to systematically uncover horizontal transfer events. Expanding such efforts across a wide range of species will generate novel insights into the relative frequency of horizontal transfer of different TEs and provide the evolutionary context of these lateral transfer events.


Asunto(s)
Culicidae/clasificación , Culicidae/genética , Elementos Transponibles de ADN/genética , Transferencia de Gen Horizontal/fisiología , Especiación Genética , Animales , Secuencia de Bases , Secuenciación de Nucleótidos de Alto Rendimiento/métodos , Hibridación Fluorescente in Situ , Datos de Secuencia Molecular , Filogenia , Especificidad de la Especie , Factores de Tiempo
2.
Science ; 316(5832): 1718-23, 2007 Jun 22.
Artículo en Inglés | MEDLINE | ID: mdl-17510324

RESUMEN

We present a draft sequence of the genome of Aedes aegypti, the primary vector for yellow fever and dengue fever, which at approximately 1376 million base pairs is about 5 times the size of the genome of the malaria vector Anopheles gambiae. Nearly 50% of the Ae. aegypti genome consists of transposable elements. These contribute to a factor of approximately 4 to 6 increase in average gene length and in sizes of intergenic regions relative to An. gambiae and Drosophila melanogaster. Nonetheless, chromosomal synteny is generally maintained among all three insects, although conservation of orthologous gene order is higher (by a factor of approximately 2) between the mosquito species than between either of them and the fruit fly. An increase in genes encoding odorant binding, cytochrome P450, and cuticle domains relative to An. gambiae suggests that members of these protein families underpin some of the biological differences between the two mosquito species.


Asunto(s)
Aedes/genética , Genoma de los Insectos , Insectos Vectores/genética , Aedes/metabolismo , Animales , Anopheles/genética , Anopheles/metabolismo , Arbovirus , Secuencia de Bases , Elementos Transponibles de ADN , Dengue/prevención & control , Dengue/transmisión , Drosophila melanogaster/genética , Femenino , Genes de Insecto , Humanos , Proteínas de Insectos/genética , Insectos Vectores/metabolismo , Masculino , Proteínas de Transporte de Membrana/genética , Datos de Secuencia Molecular , Familia de Multigenes , Estructura Terciaria de Proteína/genética , Análisis de Secuencia de ADN , Caracteres Sexuales , Procesos de Determinación del Sexo , Especificidad de la Especie , Sintenía , Transcripción Genética , Fiebre Amarilla/prevención & control , Fiebre Amarilla/transmisión
3.
Mol Biol Evol ; 20(11): 1811-25, 2003 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-12832632

RESUMEN

Over a hundred families of non-long terminal repeat retrotransposons (non-LTRs) were found in the newly released Anopheles gambiae genome assembly during a reiterative and comprehensive search using the conserved reverse transcriptase (RT) domains of known non-LTRs as the starting queries. These families, which are defined by at least 20% amino acid sequence divergence in their RT domains, range from a few to approximately 2,000 copies and occupy at least 3% of the genome. In addition to having an unprecedented number of diverse families, A. gambiae non-LTRs represent 8 of the 15 previously defined clades plus two novel clades, Loner and Outcast, more than what has been reported for any genome. Five families were found belonging to the L1 clade, which had no invertebrate representatives to date. One unique family named Sponge contains only a complete open reading frame (ORF) for the Gag-like protein and appears to have been mobilized by a family of the CR1 clade. Although most families appear to be inactive as expected, all clades except R4 have families with characteristics suggesting recent activity. At least 21 families have multiple full-length copies with over 99% nucleotide identity and some or all of the following characteristics: target site duplications (TSDs), intact ORFs, and corresponding expressed sequence tags (ESTs). The incredible diversity and the maintenance of multiple recently active lineages within different clades indicate a complex evolutionary scenario. A. gambiae non-LTRs have the potential to be developed as tools for population genetic studies and genetic manipulations of this primary vector of the devastating disease malaria. The semi-automated reiterative search approach described here may be used with any genome assembly to systematically survey and characterize non-LTRs as well as other transposable elements that encode a conserved protein.


Asunto(s)
Anopheles/genética , Retroelementos/genética , Secuencias Repetidas Terminales/genética , Animales , Secuencia de Bases , Secuencia Conservada , Elementos Transponibles de ADN , Bases de Datos como Asunto , Evolución Molecular , Etiquetas de Secuencia Expresada , Genes de Insecto , Genoma , Modelos Genéticos , Datos de Secuencia Molecular , Sistemas de Lectura Abierta , Filogenia , Estructura Terciaria de Proteína , Homología de Secuencia de Ácido Nucleico , Programas Informáticos
4.
Science ; 298(5591): 129-49, 2002 Oct 04.
Artículo en Inglés | MEDLINE | ID: mdl-12364791

RESUMEN

Anopheles gambiae is the principal vector of malaria, a disease that afflicts more than 500 million people and causes more than 1 million deaths each year. Tenfold shotgun sequence coverage was obtained from the PEST strain of A. gambiae and assembled into scaffolds that span 278 million base pairs. A total of 91% of the genome was organized in 303 scaffolds; the largest scaffold was 23.1 million base pairs. There was substantial genetic variation within this strain, and the apparent existence of two haplotypes of approximately equal frequency ("dual haplotypes") in a substantial fraction of the genome likely reflects the outbred nature of the PEST strain. The sequence produced a conservative inference of more than 400,000 single-nucleotide polymorphisms that showed a markedly bimodal density distribution. Analysis of the genome sequence revealed strong evidence for about 14,000 protein-encoding transcripts. Prominent expansions in specific families of proteins likely involved in cell adhesion and immunity were noted. An expressed sequence tag analysis of genes regulated by blood feeding provided insights into the physiological adaptations of a hematophagous insect.


Asunto(s)
Anopheles/genética , Genes de Insecto , Genoma , Análisis de Secuencia de ADN , Animales , Anopheles/clasificación , Anopheles/parasitología , Anopheles/fisiología , Evolución Biológica , Sangre , Inversión Cromosómica , Cromosomas Artificiales Bacterianos , Biología Computacional , Elementos Transponibles de ADN , Digestión , Drosophila melanogaster/genética , Enzimas/química , Enzimas/genética , Enzimas/metabolismo , Etiquetas de Secuencia Expresada , Conducta Alimentaria , Regulación de la Expresión Génica , Variación Genética , Haplotipos , Humanos , Proteínas de Insectos/química , Proteínas de Insectos/genética , Proteínas de Insectos/fisiología , Insectos Vectores/genética , Insectos Vectores/parasitología , Insectos Vectores/fisiología , Malaria Falciparum/transmisión , Datos de Secuencia Molecular , Control de Mosquitos , Mapeo Físico de Cromosoma , Plasmodium falciparum/crecimiento & desarrollo , Polimorfismo de Nucleótido Simple , Proteoma , Especificidad de la Especie , Factores de Transcripción/química , Factores de Transcripción/genética , Factores de Transcripción/fisiología
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