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Chinese Journal of Medical Genetics ; (6): 330-332, 2006.
Article Dans Chinois | WPRIM | ID: wpr-263783

Résumé

<p><b>OBJECTIVE</b>To construct the NLS(ING1)-GFP vector, transfer it into MRC-5 cells and establish a cell model expressing NLS (ING1)-GFP fusion protein.</p><p><b>METHODS</b>Firstly, cDNA fragment of nuclear locating sequence (NLS) of inhibitor of growth-1 gene (ING1) was gained by RT-PCR and inserted into multi-clone site of pEGFP-C1 to construct the NLS (ING1)-GFP expression vector. Then the vector was used to transfect the MRC-5 cells to observe the subcellular signal localization of green fluorescence protein (GFP).</p><p><b>RESULTS</b>We successfully constructed the expressing vector of NLS (ING1)-GFP fusion protein. After transferring the fusion expressing vector into MRC-5 cells, we observed that green fluorescence signal located in the cell nucleus. However, the green fluorescence signal located in the cytoplasm in MRC-5 cells transfected with pEGFP-C1 control only expressing GFP.</p><p><b>CONCLUSION</b>In living cells, physiologically p33 ING1b locates absolutely in nucleus. The p33(ING1b) NLS plays a decisive role in the transporting process of subcellular localization.</p>


Sujets)
Humains , Séquence nucléotidique , Lignée cellulaire , Vecteurs génétiques , Génétique , Protéines à fluorescence verte , Génétique , Métabolisme , Protéine-1 d'inhibition de croissance , Protéines et peptides de signalisation intracellulaire , Génétique , Métabolisme , Microscopie de fluorescence , Données de séquences moléculaires , Protéines nucléaires , Génétique , Métabolisme , Protéines de fusion recombinantes , Génétique , Métabolisme , RT-PCR , Analyse de séquence d'ADN , Transfection , Protéines suppresseurs de tumeurs , Génétique , Métabolisme
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