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1.
Insect Biochem Mol Biol ; 123: 102917, 2020 08.
Artigo em Inglês | MEDLINE | ID: mdl-28119199

RESUMO

Aphids are emerging as model organisms for both basic and applied research. Of the 5,000 estimated species, only three aphids have published whole genome sequences: the pea aphid Acyrthosiphon pisum, the Russian wheat aphid, Diuraphis noxia, and the green peach aphid, Myzus persicae. We present the whole genome sequence of a fourth aphid, the soybean aphid (Aphis glycines), which is an extreme specialist and an important invasive pest of soybean (Glycine max). The availability of genomic resources is important to establish effective and sustainable pest control, as well as to expand our understanding of aphid evolution. We generated a 302.9 Mbp draft genome assembly for Ap. glycines using a hybrid sequencing approach. This assembly shows high completeness with 19,182 predicted genes, 92% of known Ap. glycines transcripts mapping to contigs, and substantial continuity with a scaffold N50 of 174,505 bp. The assembly represents 95.5% of the predicted genome size of 317.1 Mbp based on flow cytometry. Ap. glycines contains the smallest known aphid genome to date, based on updated genome sizes for 19 aphid species. The repetitive DNA content of the Ap. glycines genome assembly (81.6 Mbp or 26.94% of the 302.9 Mbp assembly) shows a reduction in the number of classified transposable elements compared to Ac. pisum, and likely contributes to the small estimated genome size. We include comparative analyses of gene families related to host-specificity (cytochrome P450's and effectors), which may be important in Ap. glycines evolution. This Ap. glycines draft genome sequence will provide a resource for the study of aphid genome evolution, their interaction with host plants, and candidate genes for novel insect control methods.


Assuntos
Afídeos/genética , Genoma de Inseto , Animais , Evolução Biológica , Sistema Enzimático do Citocromo P-450/genética , Elementos de DNA Transponíveis/genética , Tamanho do Genoma , Genômica , Controle de Pragas , Filogenia , Glycine max
2.
Heredity (Edinb) ; 120(1): 25-37, 2018 01.
Artigo em Inglês | MEDLINE | ID: mdl-29234172

RESUMO

Human-mediated changes in landscapes can facilitate niche expansion and accelerate the adaptation of insect species. The interaction between the evolutionary history of the sugarcane borer, Diatraea saccharalis Fabricius, and historical and modern agricultural activity in Brazil shaped its spatial genetic structure, facilitating ecological divergence and incipient host shifting. Based on microsatellite data, STRUCTURE analyses identified two (K = 2) and three (K = 3) significant genetic clusters that corresponded to: (a) a strong signal of spatial genetic structure and, (b) a cryptic signal of host differentiation. We inferred that K = 2 reflects the footprint of agricultural activity, such as expansion of crop production (sugarcane and maize), unintentional dispersion of pests, and management practices. In contrast, K = 3 indicated incipient host differentiation between larvae collected from sugarcane or maize. Our estimates of population size changes indicated that a historical bottleneck was associated with a reduction of sugarcane production ≈200 years ago. However, a more recent population expansion was detected (>1950s), associated with agricultural expansion of large crop production into previously unfarmed land. Partial Mantel tests supported our hypothesis of incipient host adaptation, and identified isolation-by-environment (e.g., host plant) in São Paulo and Minas Gerais states, where sugarcane has been traditionally produced in Brazil. The impact of agricultural production on D. saccharalis may continue, as the current population structure may hinder the efficacy of refuge plants in delaying insect resistance evolution to Bt toxin.


Assuntos
Agricultura/métodos , Ecossistema , Mariposas/fisiologia , Saccharum/parasitologia , Agricultura/tendências , Animais , Brasil , Fluxo Gênico , Genótipo , Geografia , Interações Hospedeiro-Parasita , Humanos , Larva/genética , Larva/fisiologia , Repetições de Microssatélites/genética , Mariposas/classificação , Mariposas/genética , Filogenia , Dinâmica Populacional , Saccharum/crescimento & desenvolvimento , Zea mays/crescimento & desenvolvimento , Zea mays/parasitologia
3.
Genet Mol Biol ; 34(4): 719-25, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22215980

RESUMO

The applicability of mitochondrial nad6 sequences to studies of DNA and population variability in Lepidoptera was tested in four species of economically important moths and one of wild butterflies. The genetic information so obtained was compared to that of cox1 sequences for two species of Lepidoptera. nad6 primers appropriately amplified all the tested DNA targets, the generated data proving to be as informative and suitable in recovering population structures as that of cox1. The proposal is that, to obtain more robust results, this mitochondrial region can be complementarily used with other molecular sequences in studies of low level phylogeny and population genetics in Lepidoptera.

4.
Genet. mol. biol ; 34(4): 719-725, 2011. graf
Artigo em Inglês | LILACS | ID: lil-605948

RESUMO

The applicability of mitochondrial nad6 sequences to studies of DNA and population variability in Lepidoptera was tested in four species of economically important moths and one of wild butterflies. The genetic information so obtained was compared to that of cox1 sequences for two species of Lepidoptera. nad6 primers appropriately amplified all the tested DNA targets, the generated data proving to be as informative and suitable in recovering population structures as that of cox1. The proposal is that, to obtain more robust results, this mitochondrial region can be complementarily used with other molecular sequences in studies of low level phylogeny and population genetics in Lepidoptera.


Assuntos
Animais , DNA Mitocondrial , Variação Genética , Lepidópteros/genética , Borboletas , Complexo IV da Cadeia de Transporte de Elétrons , Genética Populacional , Análise de Sequência de DNA
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