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1.
Biosci Biotechnol Biochem ; 79(3): 367-73, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25496401

RESUMO

The coelomic cells of the earthworm consist of leukocytes, chlorogocytes, and coelomocytes, which play an important role in innate immunity reactions. To gain insight into the expression profiles of coelomic cells of the earthworm, Eisenia andrei, we analyzed 1151 expressed sequence tags (ESTs) derived from the cDNA library of the coelomic cells. Among the 1151 ESTs analyzed, 493 ESTs (42.8%) showed a significant similarity to known genes and represented 164 unique genes, of which 93 ESTs were singletons and 71 ESTs manifested as two or more ESTs. From the 164 unique genes sequenced, we found 24 immune-related and cell defense genes. Furthermore, real-time PCR analysis showed that levels of lysenin-related proteins mRNA in coelomic cells of E. andrei were upregulated after the injection of Bacillus subtilis bacteria. This EST data-set would provide a valuable resource for future researches of earthworm immune system.


Assuntos
Etiquetas de Sequências Expressas/metabolismo , Perfilação da Expressão Gênica , Oligoquetos/genética , Oligoquetos/imunologia , Sequência de Aminoácidos , Animais , Sequência de Bases , Escherichia coli/fisiologia , Regulação da Expressão Gênica , Análise em Microsséries , Dados de Sequência Molecular , Oligoquetos/citologia , Oligoquetos/microbiologia , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Toxinas Biológicas/química , Toxinas Biológicas/genética , Toxinas Biológicas/metabolismo
2.
Biosci Biotechnol Biochem ; 73(1): 29-34, 2009 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19129665

RESUMO

In order to gain insight into the gene expression profiles associated with anterior regeneration of the earthworm, Perionyx excavatus, we analyzed 1,159 expressed sequence tags (ESTs) derived from cDNA library early anterior regenerated tissue. Among the 1,159 ESTs analyzed, 622 (53.7%) ESTs showed significant similarity to known genes and represented 338 genes, of which 233 ESTs were singletons and 105 ESTs manifested as two or more ESTs. While 663 ESTs (57.2%) were sequenced only once, 308 ESTs (26.6%) appeared 2 to 5 times, and 188 ESTs (16.2%) were sequenced more than 5 times. A total of 803 genes were categorized into 15 groups according to their biological functions. Among 1,159 ESTs sequenced, we found several gene encoding signaling molecules, such as Notch and Distal-less. The ESTs used in this study should provide a resource for future research in earthworm regeneration.


Assuntos
Impressões Digitais de DNA/métodos , Etiquetas de Sequências Expressas , Regeneração/genética , Animais , Biblioteca Gênica , Proteínas de Homeodomínio/genética , Proteínas de Homeodomínio/fisiologia , Oligoquetos , Receptores Notch/genética , Receptores Notch/fisiologia , Fatores de Transcrição/genética , Fatores de Transcrição/fisiologia
3.
Biol Pharm Bull ; 32(2): 253-8, 2009 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19182385

RESUMO

We have cloned an earthworm-derived Factor Xa (FXa) inhibitor, with an excellent inhibitory specificity from the midgut of the Eisenia andrei. We designate this inhibitor eisenstasin. An eisenstasin-derived small peptide (ESP) was synthesized and we examined whether ESP played an essential role in FXa inhibition. Compared to antistasin-derived small peptides (ASP) originating from leech, ESP primarily exhibited a high level of FXa inhibition in chromogenic peptide substrate assays and revealed an approximately 2-fold greater inhibition of FXa cleavage of a target protein than ASP. This suggests that ESP could be an effective anti-coagulant that targets FXa during the propagation step of coagulation. ESP also inhibited proteinase-activated receptor 2-mediated FXa activation, which may trigger endothelial inflammation. Endothelial nitric oxide (NO) was significantly reduced by ESP (p<0.0001), indicating that protease-activated receptor-2 (PAR-2) was effectively inactivated. We also found that ESP reduced the expressions of pro-inflammatory cytokines (IL-1alpha, IL-1beta, IL-8, IL-16, MCP-1, MIP-1alpha and MIP-1beta) by cultured cells treated with both ESP and FXa. Our results provide the first evidence that ESP might interrupt coagulation cascades by inhibiting FXa, and thereby may effectively control the bidirectional alternation between coagulation and inflammation.


Assuntos
Anti-Inflamatórios não Esteroides/farmacologia , Anticoagulantes/farmacologia , Inibidores do Fator Xa , Hormônios de Invertebrado/farmacologia , Oligoquetos/metabolismo , Animais , Anti-Inflamatórios não Esteroides/síntese química , Anticoagulantes/síntese química , Antineoplásicos/farmacologia , Western Blotting , Linhagem Celular , Citocinas/biossíntese , Ensaios de Seleção de Medicamentos Antitumorais , MAP Quinases Reguladas por Sinal Extracelular/antagonistas & inibidores , MAP Quinases Reguladas por Sinal Extracelular/metabolismo , Fator Xa/farmacologia , Humanos , Hormônios de Invertebrado/síntese química , Óxido Nítrico/metabolismo , Fosforilação , Receptor PAR-1/biossíntese , Receptor PAR-1/genética
4.
Dev Genes Evol ; 216(9): 551-3, 2006 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16609868

RESUMO

A ParaHox gene cluster is composed of three genes (Gsx, Xlox, and Cdx). It has been proposed that all three ParaHox genes were present in the last common ancestor to the lophotrochozoan protostomes and the deuterostomes and that gene loss event has occurred in the ecdysozoan lineage. In this paper, we report the existence of all three ParaHox genes in Perionyx excavatus, a clitellate annelid. Although orthologs of each of the three ParaHox genes were previously discovered from other lopotrochozoan taxa, this study constitutes the first reported isolation of all three ParaHox genes in the same clitellate species.


Assuntos
Genes Homeobox , Oligoquetos/genética , Sequência de Aminoácidos , Animais , Dados de Sequência Molecular , Família Multigênica
5.
Biochem Biophys Res Commun ; 328(4): 1196-204, 2005 Mar 25.
Artigo em Inglês | MEDLINE | ID: mdl-15708003

RESUMO

In order to gain insight into the expression profiles of the earthworm midgut, we analyzed 1106 expressed sequence tags (ESTs) derived from the earthworm midgut cDNA library. Among the 1106 ESTs analyzed, 557 (50.4%) ESTs showed significant similarity to known genes and represented 229 unique genes of which 166 ESTs were singletons and 63 ESTs manifest as two or more ESTs. While 552 ESTs (49.9%) were sequenced only once, 230 ESTs (20.8%) appeared two to five times and 324 ESTs (29.3%) were sequenced more than five times. Considering this redundancy of expression, it is likely that the gene expression profile of the earthworm midgut would be polarized. The expression of globin-related proteins, including ferritin and linker chain, and fibrinolytic enzymes appeared to account for 10.1% and 4.7% of the total ESTs analyzed in this study, respectively. This suggests that the prime functions of the midgut in the earthworm would be associated with protein hydrolysis as well as globin formation. Among the recognized protein-coding genes, the gene category involved in protein synthesis appeared to be the largest one accounting for 15.6% of the expression in the midgut, followed by gene categories associated with energy (11.2%), homeostasis (10.8%), metabolism (3.6%), cytoskeleton (2.5%), and protein fate (1.4%). With regard to functional aspects, the most abundantly expressed genes were associated with respiratory pigment (10.1%), cellular respiration (8.6%), and fibrin hydrolysis (4.7%). In addition, we were able to identify novel ESTs in the earthworm, which were related to the innate immune system, including destabilase, a possible antagonist of transglutaminase.


Assuntos
Mucosa Intestinal/metabolismo , Oligoquetos/genética , Oligoquetos/metabolismo , Proteoma/genética , Proteoma/metabolismo , Fatores de Transcrição/genética , Fatores de Transcrição/metabolismo , Animais , Sequência de Bases , Mapeamento Cromossômico/métodos , Etiquetas de Sequências Expressas , Perfilação da Expressão Gênica/métodos , Regulação da Expressão Gênica/fisiologia , Dados de Sequência Molecular , Análise de Sequência de DNA/métodos
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