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1.
Gene ; 393(1-2): 145-52, 2007 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-17566170

RESUMO

Differentially expressed genes in response to rust infection (Puccinia sp.) in creeping red fescue (Festuca rubra var. rubra) were identified and quantified using the mRNA differential display technique. The differentially induced genes were identified as homologs of mitogen-activated protein kinase (MAPK) 3 of Arabidopsis thaliana, stem rust resistance protein Rpg1 of barley and Hsp70 of Spinacia oleracea. The change in the steady state expression levels of these genes in response to rust infection was tested by Northern blot analysis and further quantified by real-time PCR. A steady accumulation of transcripts in the course of rust infection was observed. Full-length transcript of a fescue MPK-3 was obtained by RACE PCR. Its corresponding cDNA encodes a protein with a predicted MW of 42.5 kDa which was mapped onto the structural model of homologs MAPK to illustrate the corresponding MAPK signature motifs. This study, for the first time, presents evidence on the rust infection dependent metabolic pathways in creeping red fescue.


Assuntos
Festuca/genética , Festuca/microbiologia , Fungos/fisiologia , Regulação da Expressão Gênica de Plantas/genética , Doenças das Plantas/genética , Doenças das Plantas/microbiologia , Sequência de Aminoácidos , Clonagem Molecular , DNA Complementar/genética , DNA Complementar/metabolismo , Festuca/classificação , Festuca/enzimologia , Proteínas Quinases Ativadas por Mitógeno/química , Proteínas Quinases Ativadas por Mitógeno/genética , Modelos Biológicos , Modelos Moleculares , Dados de Sequência Molecular , Folhas de Planta/genética , Folhas de Planta/microbiologia , Conformação Proteica , RNA Mensageiro/análise , RNA Mensageiro/genética , RNA de Plantas/genética , RNA de Plantas/metabolismo
2.
Clin Res Hepatol Gastroenterol ; 37(4): 359-64, 2013 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-23273495

RESUMO

BACKGROUND: Chronic hepatitis B treatment with oral antiviral drugs is a long course. During this course, antiviral resistance is a serious issue, particularly, if genetically low barrier drugs are in use. Host immunity is accepted to have an effect on antiviral resistance development. The earliest clinical sign of drug resistance is virologic breakthrough. In this study, we aimed to investigate the relation between HLA-DQB1 alleles and virologic breakthrough events. SUBJECTS AND METHODS: The patient records at single institution hepatology clinic were reviewed. Local institution ethics committee approval was taken. The patients' demographic data, virologic parameters, treatment statues were noted. Patients who had received lamivudine or adefovir were recruited and grouped into two according to virologic breakthrough occurrence. Patients who were not compliant to the given treatment were excluded. Blood samples were taken for DNA extraction. HLA-DQB1 alleles were determined at high level by sequence-specific primers-polymerase chain reaction. The distribution of DQB1 alleles among groups was analyzed. RESULTS: One hundred ninety-eight patients were eligible for the study. Ninety-six of them had virologic breakthrough where 102 did not have. DQB1 0503 allele was more frequent in patients without breakthrough (28.4% vs. 12.4%, P=0.006). In univariate analysis, HBeAg seropositivity (P<0.001), absence of cirrhosis (P=0.007), younger age (P=0.002) and higher pretreatment logDNA (P<0.001) were related to breakthrough events. However, in multivariate analysis only logDNA (P<0.001) and DQB1*0503 (P=0.02) allele revealed statistically significant relation with breakthrough events. CONCLUSION: Host immunity may have an effect on outcome during treatment with oral antiviral drugs. A patient with better immunologic profile may suppress the viral replication better and this may cause less resistance occurrence during treatment with genetically low barrier drugs.


Assuntos
Adenina/análogos & derivados , Antivirais/farmacologia , Antivirais/uso terapêutico , Cadeias beta de HLA-DQ/genética , Vírus da Hepatite B/efeitos dos fármacos , Vírus da Hepatite B/genética , Hepatite B Crônica/tratamento farmacológico , Hepatite B Crônica/virologia , Lamivudina/farmacologia , Lamivudina/uso terapêutico , Organofosfonatos/farmacologia , Organofosfonatos/uso terapêutico , Adenina/farmacologia , Adenina/uso terapêutico , Adulto , Alelos , Farmacorresistência Viral , Feminino , Hepatite B Crônica/sangue , Humanos , Masculino , RNA Viral/sangue
3.
Biochem Genet ; 46(9-10): 663-76, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18726683

RESUMO

Bentgrass (Agrostis spp.), a genus of the Poaceae family, consists of more than 200 species and is mainly used in athletic fields and golf courses. Creeping bentgrass (A. stolonifera L.) is the most commonly used species in maintaining golf courses, followed by colonial bentgrass (A. capillaris L.) and velvet bentgrass (A. canina L.). The presence and nature of sequence related amplified polymorphism (SRAP) at the cDNA level were investigated. We isolated 80 unique cDNA fragment bands from these species using 56 SRAP primer combinations. Sequence analysis of cDNA clones and analysis of putative translation products revealed that some encoded amino acid sequences were similar to proteins involved in DNA synthesis, transcription, and signal transduction. The cytosolic glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene (GenBank accession no. EB812822) was also identified from velvet bentgrass, and the corresponding protein sequence is further analyzed due to its critical role in many cellular processes. The partial peptide sequence obtained was 112 amino acids long, presenting a high degree of homology to parts of the N-terminal and C-terminal regions of cytosolic phosphorylating GAPDH (GapC). The existence of common expressed sequence tags (ESTs) revealed by a minimum evolutionary dendrogram among the Agrostis ESTs indicated the usefulness of SRAP for comparative genome analysis of transcribed genes in the grass species.


Assuntos
Agrostis/genética , Etiquetas de Sequências Expressas , Polimorfismo Genético , Sequência de Aminoácidos , Clonagem Molecular , Citosol/metabolismo , DNA Complementar/metabolismo , Biblioteca Gênica , Gliceraldeído 3-Fosfato Desidrogenase (NADP+)/metabolismo , Conformação Molecular , Dados de Sequência Molecular , Filogenia , Sementes/metabolismo , Homologia de Sequência de Aminoácidos , Transdução de Sinais
4.
Mol Cell ; 26(1): 27-39, 2007 Apr 13.
Artigo em Inglês | MEDLINE | ID: mdl-17434124

RESUMO

Hsp70 chaperones assist in protein folding, disaggregation, and membrane translocation by binding to substrate proteins with an ATP-regulated affinity that relies on allosteric coupling between ATP-binding and substrate-binding domains. We have studied single- and two-domain versions of the E. coli Hsp70, DnaK, to explore the mechanism of interdomain communication. We show that the interdomain linker controls ATPase activity by binding to a hydrophobic cleft between subdomains IA and IIA. Furthermore, the domains of DnaK dock only when ATP binds and behave independently when ADP is bound. Major conformational changes in both domains accompany ATP-induced docking: of particular importance, some regions of the substrate-binding domain are stabilized, while those near the substrate-binding site become destabilized. Thus, the energy of ATP binding is used to form a stable interface between the nucleotide- and substrate-binding domains, which results in destabilization of regions of the latter domain and consequent weaker substrate binding.


Assuntos
Regulação Alostérica , Proteínas de Escherichia coli/metabolismo , Proteínas de Choque Térmico HSP70/química , Proteínas de Choque Térmico HSP70/metabolismo , Ligantes , Difosfato de Adenosina/química , Adenosina Trifosfatases/química , Adenosina Trifosfatases/metabolismo , Trifosfato de Adenosina/metabolismo , Sítios de Ligação , Medição da Troca de Deutério , Proteínas de Escherichia coli/química , Interações Hidrofóbicas e Hidrofílicas , Espectroscopia de Ressonância Magnética , Modelos Químicos , Nucleotídeos/química , Estrutura Terciária de Proteína , Relação Estrutura-Atividade , Especificidade por Substrato
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