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1.
Mitochondrial DNA B Resour ; 8(9): 989-992, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37746031

RESUMO

Anabarilius duoyiheensis is a native and rare fish in Yunnan. In this study, the complete mitochondrial genome of A. duoyiheensis was sequenced and published for a total of 16,614 bp, including 13 protein-coding genes, 22 transfer RNAs, two ribosomal RNAs, and one control region. The phylogenetic analysis based on the complete mitochondrial genome showed that A. duoyiheensis belongs to the clade of the genus Anabarilius and was sister to the clade of Hemiculter. This study also contributes to the genus phylogeny of Anabarilius and other members of the family Xenocyprididae.

2.
Mol Plant Pathol ; 15(4): 333-41, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24286630

RESUMO

Bacterial blight (BB), caused by Xanthomonas oryzae pv. oryzae (Xoo), is not only a disease devastating rice production worldwide, but also an ideal model system for the study of the interaction between plants and their bacterial pathogens. The rice near-isogenic line (NIL) CBB23, derived from a cross between a wild rice Oryza rufipogon accession (RBB16) and a susceptible indica rice variety (Jingang 30), is highly resistant to all field Xoo strains tested so far. Although the BB resistance of CBB23 has been widely used in rice breeding programmes, the mechanism of its extremely broad-spectrum resistance remains unknown. Here, we report the molecular cloning of an avirulence gene, designated as avrXa23, from Xoo strain PXO99(A) . We validate that AvrXa23, a novel transcription activator-like effector, specifically triggers the broad-spectrum BB resistance in CBB23. The prevalence of avrXa23 in all 38 Xoo strains surveyed may explain the broad-spectrum feature of BB resistance in CBB23. The results will significantly facilitate the molecular cloning of the corresponding resistance (R) gene in the host, and provide new insights into our understanding of the molecular mechanism for broad-spectrum disease resistance in plants.


Assuntos
Proteínas de Bactérias/metabolismo , Oryza/metabolismo , Oryza/parasitologia , Doenças das Plantas/microbiologia , Xanthomonas/patogenicidade , Regulação da Expressão Gênica de Plantas , Dados de Sequência Molecular
3.
Mol Biol Rep ; 39(2): 2011-20, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21633886

RESUMO

The gayal (Bos frontalis) is a rare semi-wild bovid species in which bovine spongiform encephalopathy (BSE) has not been reported. Polymorphisms of the prion protein gene (PRNP) have been correlated significantly with resistance to BSE. In this study, the coding region of PRNP was cloned and characterized in samples from 125 gayal. A total of ten single nucleotide polymorphisms (SNPs), including six silent mutations (C60T, G75A, A108T, G126A, C357T and C678T) and four mis-sense mutations (C8A, G145A, G461A and C756G), corresponding to amino acids T3K, G49S9, N154S and I252M were identified, revealing high genetic diversity. Three novel SNPs including C60T, G145A and C756G, which have not been reported previously in bovid species, were retrieved. There also was one insertion-deletion (187Del24) at the N-terminal octapeptide repeat region. Alignment of nucleotide and amino acid sequences showed a high degree of similarity with other bovid species. Using phylogenetic analyses it was revealed that gayal has a close genetic relationship with Zebu cattle. In short, preliminary information is provided about genotypes of the PRNP in gayal. This could assist with the study of the pathogenesis of transmissible spongiform encephalopathies and cross species transmission as well as a molecular breeding project for gayal in China.


Assuntos
Bovinos/genética , Resistência à Doença/genética , Encefalopatia Espongiforme Bovina/genética , Variação Genética/genética , Modelos Moleculares , Filogenia , Príons/genética , Sequência de Aminoácidos , Animais , Sequência de Bases , Clonagem Molecular , Biologia Computacional , Primers do DNA/genética , Frequência do Gene , Genótipo , Haplótipos/genética , Dados de Sequência Molecular , Fases de Leitura Aberta/genética , Polimorfismo de Nucleotídeo Único/genética , Conformação Proteica , Alinhamento de Sequência , Análise de Sequência de DNA
4.
Mol Biol Rep ; 37(1): 39-45, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19340603

RESUMO

The complete coding sequences of two sheep genes--LCK and CDK2--were amplified using the rapid amplification of cDNA ends method based on three sheep EST sequences whose translated amino acids contain the domain PTKc_Lck_BIk and S_TKc domain, respectively. The sequence analyses of these two genes revealed that the sheep LCK gene encodes a protein of 509 amino acids which has high homology with the lymphocyte-specific protein tyrosine kinase (LCK) of eight species: bovine (99%), human (96%), dog (96%), Aotus nancymaae (95%), mouse (94%), rat (91%), horse (91%) and chicken (81%). The sheep CDK2 gene encodes a protein of 298 amino acids which has high homology with the cyclin-dependent kinase 2 (CDK2) of ten species: bovine (100%), goat (100%), rat (99%), mouse (99%), Chinese hamster (99%), dog (98%), golden hamster (98%), human (98%), horse (98%) and rhesus monkey (98%). The tissue transcription profile analyses indicated that that the Black-boned sheep LCK and CDK2 genes are generally but differentially expressed in the detected tissues including in tissues including spleen, muscle, skin, kidney, lung, liver and heart. These data serve as a foundation for further insight into these two genes.


Assuntos
Quinase 2 Dependente de Ciclina/genética , Perfilação da Expressão Gênica , Proteína Tirosina Quinase p56(lck) Linfócito-Específica/genética , Especificidade de Órgãos/genética , Análise de Sequência de DNA , Ovinos/genética , Sequência de Aminoácidos , Animais , Sequência de Bases , Clonagem Molecular , Quinase 2 Dependente de Ciclina/química , Humanos , Proteína Tirosina Quinase p56(lck) Linfócito-Específica/química , Dados de Sequência Molecular , Filogenia , Reação em Cadeia da Polimerase , Estrutura Secundária de Proteína , Estrutura Terciária de Proteína , Alinhamento de Sequência
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