Pregled bibliografske jedinice broj: 49337
Optimal conditions for in vitro reconstitution of small nuclear ribonucleoprotein particles
Optimal conditions for in vitro reconstitution of small nuclear ribonucleoprotein particles // Croatian Medical Journal, 37 (1996), 2; 75-80 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 49337 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Optimal conditions for in vitro reconstitution of small nuclear ribonucleoprotein particles
Autori
Pećina-Šlaus, Nives
Izvornik
Croatian Medical Journal (0353-9504) 37
(1996), 2;
75-80
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
ribonucleoproteins; small nuclear; RNA splicing; RNA; small nuclear
Sažetak
Aim. Optimization of conditions required for the in vitro reconstitution of small nuclear ribonucleoprotein particles (snRNPs) of the U family using different parameters. Method. Individual snRNPs were reconstituted by adding each small nuclear RNA of the "U" family to the snRNP protein pool obtained from S 100 HeLa cytoplasmic extract. The mixture was then immunoprecipitated with anti-trimethylguanosine (aTMG) monoclonal antibody, followed by polyacrylamide gel electrophoresis and autoradiography. Results. U1 required 0.5 nuclear extract equivalents of U1 snRNA, 6 mM MgCl2 and incubation at 30oC for 30 minutes ; U2 required 0.5 nuclear extract equivalents of U2 snRNA, the same conditions as above but without Mg++ ions. U4 was reconstituted by incubating it for 20 minutes at 30oC and for another 10 at 37oC without Mg++ ions. U5 required 2 nuclear extract equivalents of U5 snRNA, 6 mM MgCl2 and incubation for 30 minutes at 30oC. U4/U6 needed 0.5 nuclear extract equivalents of each snRNA, and the same time and temperature as U5. U4/U5/U6 was reconstituted employing 0.5 nuclear extract equivalents of each snRNA and incubation at 30oC for 30 minutes with 6 mM MgCl2. None of the snRNPs required ATP for the reconstitution. Conclusion. The optimal conditions reported in this paper should prove useful in the elucidation of the function of snRNP specific polypeptides and eventual reconstitution of snRNPs active in splicing.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
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