Skip Navigation

This Article
Right arrow Print PDF (2860K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Brunel, C.
Right arrow Articles by Liautard, J.-P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Brunel, C.
Right arrow Articles by Liautard, J.-P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1981, Vol. 9, No. 4 815-830
© 1981


MOLECULAR BIOLOGY

Purification and characterization of a simple ribonucleoprotem particle containing small nucleoplasmic RNAs (snRNP) as a subset of RNP containing heterogenous nuclear RNA (hnRNP) from HeLa cells

Claude Brunel, Joannes Sri Widada, Marie-Noelle Lelay, Philippe Jeanteur and Jean-Pierre Liautard

Laboratoire de Biochimie, Centre Paul Lamarque B.P.No 5054, Montpellier Cedex, and Laboratoire de Biologie Moléculaire, Université des Sciences et Techniques du Languedoc Place Eugéne Bataillon, 34060 Montpellier Cedex, France

Correspondence should be addressed to : Laboratoire de Biochimie, Centre Paul Lamarque, B.P. N° 5054, 34033 MONTPELLIER CEDEX - FRANCE -

Received December 15, 1980. A ribonucleoprotein complex whose RNA complement consists exclusively of small nuclear RNA species (snRNA) has been purified from particles containing heterogenous nuclear RNA (hnRNP) from HeLa cells. This was accomplished by taking advantage of their ability to band at a density of about 1.43 g/cm3 in plain cesium chloride as well as in cesium chloride gradients containing 0.5% sarkosyl without prior aldehyde fixation. After these two steps of equilibrium density centrifugation, these snRNPs were still largely contaminated by free proteins (and especially phosphoproteins). A final step of purification by velocity sedimentation in a sucrose gradient containing 0.5 M cesium chloride and 0.5% sarkosyl was efficient in completely eliminating all free proteins. U1, U2, U4, U5 and U6 species according to the nomenclature of Lerner et al. (Nature, (1980) 283, 220–224) were found in these purified snRNPs, while a significant part U6 and a small amount of U2 were found in the bottom fraction. 5S species behaved entirely as free RNA and is presumably a contaminant of cyteplasmic origin. Electrophoresis of proteins from snRNP labeled in vivo with (35S) methionine, revealed four bands with migrations corresponding to molecular weights ranging between 10,000 and 14,000 daltons.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Genes Dev.Home page
Z Q Pan and C Prives
U2 snRNA sequences that bind U2-specific proteins are dispensable for the function of U2 snRNP in splicing.
Genes & Dev., December 1, 1989; 3(12a): 1887 - 1898.
[Abstract] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.