This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow E-mail 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 Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Potashkin, J A
Right arrow Articles by Spector, D L
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Potashkin, J A
Right arrow Articles by Spector, D L

 Previous Article  |  Next Article 

Mol Cell Biol. 1990 July; 10(7): 3524-3534

Differential distribution of factors involved in pre-mRNA processing in the yeast cell nucleus.

J A Potashkin, R J Derby and D L Spector

Cold Spring Harbor Laboratory, New York 11724.

ABSTRACT

The yeast cell nucleus has previously been shown to be divided into two regions by a variety of microscopic approaches. We used antibodies specific for the 2,2,7-trimethylguanosine cap structure of small nuclear ribonucleic acids (snRNAs) and for a protein component of small nuclear ribonucleoprotein particles to identify the distribution of small nuclear ribonucleoprotein particles within the yeast cell nucleus. These studies were performed with the fission yeast Schizosaccharomyces pombe and the budding yeast Saccharomyces cerevisiae. By using immunofluorescence microscopy and immunoelectron microscopy, most of the abundant snRNAs were localized to the portion of the nucleus which has heretofore been referred to as the nucleolus. This distribution of snRNAs is different from that found in mammalian cells and suggests that the nucleolar portion of the yeast nucleus contains functional domains in addition to those associated with RNA polymerase I activity.


Mol Cell Biol. 1990 July; 10(7): 3524-3534




This article has been cited by other articles:

  • GRAINGER, R. J., BEGGS, J. D. (2005). Prp8 protein: At the heart of the spliceosome. RNA 11: 533-557 [Abstract] [Full Text]  
  • Bubulya, P. A., Prasanth, K. V., Deerinck, T. J., Gerlich, D., Beaudouin, J., Ellisman, M. H., Ellenberg, J., Spector, D. L. (2004). Hypophosphorylated SR splicing factors transiently localize around active nucleolar organizing regions in telophase daughter nuclei. JCB 167: 51-63 [Abstract] [Full Text]  
  • Cueille, N., Salimova, E., Esteban, V., Blanco, M., Moreno, S., Bueno, A., Simanis, V. (2002). Flp1, a fission yeast orthologue of the S. cerevisiae CDC14 gene, is not required for cyclin degradation or rum1p stabilisation at the end of mitosis. J. Cell Sci. 114: 2649-2664 [Abstract] [Full Text]  
  • Ochs, R., Stein, T., Tan, E. (1994). Coiled bodies in the nucleolus of breast cancer cells. J. Cell Sci. 107: 385-399 [Abstract]  
  • Spector, D.L., O'Keefe, R.T., Jimenez-Garcia, L.F. (1993). Dynamics of Transcription and Pre-mRNA Splicing within the Mammalian Cell Nucleus. Cold Spring Harb Symp Quant Biol 58: 799-805 [Abstract]