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 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 Kraus, M E
Right arrow Articles by Lis, J T
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kraus, M E
Right arrow Articles by Lis, J T

 Previous Article  |  Next Article 

Mol Cell Biol. 1994 August; 14(8): 5360-5370

The concentration of B52, an essential splicing factor and regulator of splice site choice in vitro, is critical for Drosophila development.

M E Kraus and J T Lis

Section of Biochemistry, Molecular and Cell Biology, Cornell University, Ithaca, New York 14853.

ABSTRACT

B52 is a Drosophila melanogaster protein that plays a role in general and alternative splicing in vitro. It is homologous to the human splicing factor ASF/SF2 which is essential for an early step(s) in spliceosome assembly in vitro and also regulates 5' and 3' alternative splice site choice in a concentration-dependent manner. In vitro, B52 can function as both a general splicing factor and a regulator of 5' alternative splice site choice. Its activity in vivo, however, is largely uncharacterized. In this study, we have further characterized B52 in vivo. Using Western blot (immunoblot) analysis and whole-mount immunofluorescence, we demonstrate that B52 is widely expressed throughout development, although some developmental stages and tissues appear to have higher B52 levels than others do. In particular, B52 accumulates in ovaries, where it is packaged into the developing egg and is localized to nuclei by the late blastoderm stage of embryonic development. We also overexpressed this protein in transgenic flies in a variety of developmental and tissue-specific patterns to examine the effects of altering the concentration of this splicing factor in vivo. We show that, in many cell types, changing the concentration of B52 adversely affects the development of the organism. We discuss the significance of these observations with regard to previous in vitro results.


Mol Cell Biol. 1994 August; 14(8): 5360-5370




This article has been cited by other articles:

  • Marcucci, R., Romano, M., Feiguin, F., O'Connell, M. A., Baralle, F. E. (2009). Dissecting the splicing mechanism of the Drosophila editing enzyme; dADAR. Nucleic Acids Res 37: 1663-1671 [Abstract] [Full Text]  
  • Chung, T., Kim, C. S., Nguyen, H. N., Meeley, R. B., Larkins, B. A. (2007). The Maize Zmsmu2 Gene Encodes a Putative RNA-Splicing Factor That Affects Protein Synthesis and RNA Processing during Endosperm Development. Plant Physiol. 144: 821-835 [Abstract] [Full Text]  
  • Gabut, M., Dejardin, J., Tazi, J., Soret, J. (2007). The SR Family Proteins B52 and dASF/SF2 Modulate Development of the Drosophila Visual System by Regulating Specific RNA Targets. Mol. Cell. Biol. 27: 3087-3097 [Abstract] [Full Text]  
  • Qi, J., Su, S., McGuffin, M. E., Mattox, W. (2006). Concentration dependent selection of targets by an SR splicing regulator results in tissue-specific RNA processing. Nucleic Acids Res 34: 6256-6263 [Abstract] [Full Text]  
  • Kon, C., Cadigan, K. M., da Silva, S. L., Nusse, R. (2005). Developmental Roles of the Mi-2/NURD-Associated Protein p66 in Drosophila. Genetics 169: 2087-2100 [Abstract] [Full Text]  
  • Ryu, J.-H., Nam, K.-B., Oh, C.-T., Nam, H.-J., Kim, S.-H., Yoon, J.-H., Seong, J.-K., Yoo, M.-A., Jang, I.-H., Brey, P. T., Lee, W.-J. (2004). The Homeobox Gene Caudal Regulates Constitutive Local Expression of Antimicrobial Peptide Genes in Drosophila Epithelia. Mol. Cell. Biol. 24: 172-185 [Abstract] [Full Text]  
  • Kalyna, M., Lopato, S., Barta, A. (2003). Ectopic Expression of atRSZ33 Reveals Its Function in Splicing and Causes Pleiotropic Changes in Development. Mol. Biol. Cell 14: 3565-3577 [Abstract] [Full Text]  
  • Kim, S., Shi, H., Lee, D.-k., Lis, J. T. (2003). Specific SR protein-dependent splicing substrates identified through genomic SELEX. Nucleic Acids Res 31: 1955-1961 [Abstract] [Full Text]  
  • Allemand, E., Gattoni, R., Bourbon, H.-M., Stevenin, J., Cáceres, J. F., Soret, J., Tazi, J. (2001). Distinctive Features of Drosophila Alternative Splicing Factor RS Domain: Implication for Specific Phosphorylation, Shuttling, and Splicing Activation. Mol. Cell. Biol. 21: 1345-1359 [Abstract] [Full Text]  
  • Prasanth, K., Rajendra, T., Lal, A., Lakhotia, S. (2000). Omega speckles - a novel class of nuclear speckles containing hnRNPs associated with noncoding hsr-omega RNA in Drosophila. J. Cell Sci. 113: 3485-3497 [Abstract]  
  • Hoffman, B. E., Lis, J. T. (2000). Pre-mRNA Splicing by the Essential Drosophila Protein B52: Tissue and Target Specificity. Mol. Cell. Biol. 20: 181-186 [Abstract] [Full Text]  
  • Shi, H., Hoffman, B. E., Lis, J. T. (1999). RNA aptamers as effective protein antagonists in a multicellular organism. Proc. Natl. Acad. Sci. USA 96: 10033-10038 [Abstract] [Full Text]  
  • Lopato, S., Kalyna, M., Dorner, S., Kobayashi, R., Krainer, A. R., Barta, A. (1999). atSRp30, one of two SF2/ASF-like proteins from Arabidopsis thaliana, regulates splicing of specific plant genes. Genes Dev. 13: 987-1001 [Abstract] [Full Text]  
  • Labourier, E., Bourbon, H.-M., Gallouzi, I.-e., Fostier, M., Allemand, E., Tazi, J. (1999). Antagonism between RSF1 and SR proteins for both splice-site recognition in vitro and Drosophila development. Genes Dev. 13: 740-753 [Abstract] [Full Text]  
  • Soret, J., Gattoni, R., Guyon, C., Sureau, A., Popielarz, M., Le Rouzic, E., Dumon, S., Apiou, F., Dutrillaux, B., Voss, H., Ansorge, W., Stévenin, J., Perbal, B. (1998). Characterization of SRp46, a Novel Human SR Splicing Factor Encoded by a PR264/SC35 Retropseudogene. Mol. Cell. Biol. 18: 4924-4934 [Abstract] [Full Text]  
  • Meyer, V., Oliver, B., Pauli, D. (1998). Multiple Developmental Requirements of Noisette, the Drosophila Homolog of the U2 snRNP-Associated Polypeptide SF3a60. Mol. Cell. Biol. 18: 1835-1843 [Abstract] [Full Text]  
  • Adams, M D, Tarng, R S, Rio, D C (1997). The alternative splicing factor PSI regulates P-element third intron splicing in vivo.. Genes Dev. 11: 129-138 [Abstract]  
  • Alzhanova-Ericsson, A T, Sun, X, Visa, N, Kiseleva, E, Wurtz, T, Daneholt, B (1996). A protein of the SR family of splicing factors binds extensively to exonic Balbiani ring pre-mRNA and accompanies the RNA from the gene to the nuclear pore.. Genes Dev. 10: 2881-2893 [Abstract]  
  • Wang, J, Takagaki, Y, Manley, J L (1996). Targeted disruption of an essential vertebrate gene: ASF/SF2 is required for cell viability.. Genes Dev. 10: 2588-2599 [Abstract]