Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 2 de 2
Filtrer
Plus de filtres








Gamme d'année
1.
Article de Chinois | WPRIM | ID: wpr-269586

RÉSUMÉ

<p><b>OBJECTIVE</b>To obtain the functional information of AY358935 gene.</p><p><b>METHODS</b>The properties, subcellular location, and structure of AY358935 protein, and the expression profile of AY358935 gene were analyzed by bioinformatics software and the biological functions of the gene were predicted. AY358935 expression was detected by Western blot analysis in early virus infection.</p><p><b>RESULTS</b>AY358935 was evolutionally conserved. The human AY358935 protein had an amino acid similarity of 74%, 60%, 38% and 33% with its counterpart in horses, mice, zebrafish and Xenopus laevis, respectively. Bioinformatics analysis indicated that AY358935 protein was located likely in the mitochondria. There was a N-terminal signal peptide and single transmembrane structure in AY358935 protein, which contained several phosphorylation sites. The secondary structure mainly comprised of alpha helices and random coils. AY358935 was ubiquitously expressed in normal tissues and carcinomas and regulated by the expression of double-stranded RNA-dependent protein kinase. AY358935 protein expression was obviously upregulated in cells 2 h after infection by vesicular stomatitis virus.</p><p><b>CONCLUSION</b>As a predicted secretary protein with a small molecular weight, AY358935 might have important functions in cellular proliferation and anti-viral innate immune regulation.</p>


Sujet(s)
Humains , Séquence d'acides aminés , Chromosomes humains de la paire 11 , Génétique , Biologie informatique , Méthodes , Données de séquences moléculaires , Protéines , Génétique , Métabolisme , Similitude de séquences d'acides aminés , Logiciel , Stomatite vésiculeuse , Métabolisme
2.
Article de Chinois | WPRIM | ID: wpr-247337

RÉSUMÉ

<p><b>OBJECTIVE</b>To investigate the molecular cloning, tissue distribution, tumor distribution and the subcellular localization of AK078438 gene.</p><p><b>METHODS</b>Reverse transcriptase-polymerase chain reaction (RT-PCR) technique was applied to amplify the open reading frame of AK078438 gene. Prokaryotic expressing vector and affinity purification were used to get the fusion protein. At mRNA expressing levels semi-quantitative RT-PCR was employed for the investigation of its distribution in normal rat tissues, tumor cell and mesenchymal stem cell (MSC) lines. The eukaryotic expression green fluorescence protein (GFP) fusion protein vector was transfected into cells and identified subcellular localization.</p><p><b>RESULTS</b>The full open reading frame of AK078438 gene with 1065 bp, 355aa were identified. mRNA of the gene distributed in brain, uterus, colon, bone marrow, testis and kidney, but not in stomach, liver, the lung, spleen and heart. Murine colon adenocarcinoma C26, melanoma B16, Lewis lung carcinoma LL/2 and MSC had the gene and mouse myeloma cell line NS-1 and Hepa mouse hepatoma cell line had no the gene. The protein was localized in cytoplasm.</p><p><b>CONCLUSION</b>Protein expression, expressing profile and subcellular localization of AK078438 gene set the basis for further exploration of its functions.</p>


Sujet(s)
Animaux , Humains , Souris , Lignée cellulaire tumorale , Clonage moléculaire , Cytoplasme , Métabolisme , Analyse de profil d'expression de gènes , Régulation de l'expression des gènes , Cadres ouverts de lecture , Spécificité d'organe , Transport des protéines , Protéines , Génétique , Métabolisme , ARN messager , Génétique , Métabolisme
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE