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 Hart, C. M.
Right arrow Articles by Laemmli, U. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hart, C. M.
Right arrow Articles by Laemmli, U. K.

 Previous Article  |  Next Article 

Mol. Cell. Biol., Feb 1997, 999-1009, Vol 17, No. 2
Copyright © 1997, American Society for Microbiology

The scs' boundary element: characterization of boundary element- associated factors

CM Hart, K Zhao and UK Laemmli
Department of Biochemistry, University of Geneva, Switzerland.

Boundary elements are thought to define the peripheries of chromatin domains and to restrict enhancer-promoter interactions to their target genes within their domains. We previously characterized a cDNA encoding the BEAF-32A protein (32A), which binds with high affinity to the scs' boundary element from the Drosophila melanogaster 87A7 hsp70 locus. Here, we report a second protein, BEAF-32B, that differs from 32A only in its amino terminus. Unlike 32A, it has the same DNA binding specificity as the complete BEAF activity affinity purified from Drosophila. We characterize three domains in these proteins. Heterocomplex formation is mediated by their identical carboxy-terminal domains, and DNA binding is mediated by their unique amino-terminal domains. The identical middle domains of 32A and 32B are dispensable for the functions described here, although they may be important for boundary element function. 32A and 32B apparently form trimers, and the ratio of 32A to 32B varies at different loci on polytene chromosomes as judged by immunofluorescence. The scs' element contains a high- and low- affinity binding site for BEAF. We observed that interaction with the low-affinity site is facilitated by binding to the high-affinity site some 200 bp distant.


This article has been cited by other articles:

  • Fujioka, M., Wu, X., Jaynes, J. B. (2009). A chromatin insulator mediates transgene homing and very long-range enhancer-promoter communication. Development 136: 3077-3087 [Abstract] [Full Text]  
  • Jiang, N., Emberly, E., Cuvier, O., Hart, C. M. (2009). Genome-Wide Mapping of Boundary Element-Associated Factor (BEAF) Binding Sites in Drosophila melanogaster Links BEAF to Transcription. Mol. Cell. Biol. 29: 3556-3568 [Abstract] [Full Text]  
  • Bushey, A. M., Ramos, E., Corces, V. G. (2009). Three subclasses of a Drosophila insulator show distinct and cell type-specific genomic distributions. Genes Dev. 23: 1338-1350 [Abstract] [Full Text]  
  • Kyrchanova, O., Chetverina, D., Maksimenko, O., Kullyev, A., Georgiev, P. (2008). Orientation-dependent interaction between Drosophila insulators is a property of this class of regulatory elements. Nucleic Acids Res 36: 7019-7028 [Abstract] [Full Text]  
  • Pathak, R. U., Rangaraj, N., Kallappagoudar, S., Mishra, K., Mishra, R. K. (2007). Boundary Element-Associated Factor 32B Connects Chromatin Domains to the Nuclear Matrix. Mol. Cell. Biol. 27: 4796-4806 [Abstract] [Full Text]  
  • Roy, S., Gilbert, M. K., Hart, C. M. (2007). Characterization of BEAF Mutations Isolated by Homologous Recombination in Drosophila. Genetics 176: 801-813 [Abstract] [Full Text]  
  • Yamashita, D., Komori, H., Higuchi, Y., Yamaguchi, T., Osumi, T., Hirose, F. (2007). Human DNA Replication-related Element Binding Factor (hDREF) Self-association via hATC Domain Is Necessary for Its Nuclear Accumulation and DNA Binding. J. Biol. Chem. 282: 7563-7575 [Abstract] [Full Text]  
  • Parnell, T. J., Kuhn, E. J., Gilmore, B. L., Helou, C., Wold, M. S., Geyer, P. K. (2006). Identification of Genomic Sites That Bind the Drosophila Suppressor of Hairy-wing Insulator Protein.. Mol. Cell. Biol. 26: 5983-5993 [Abstract] [Full Text]  
  • Gilbert, M. K., Tan, Y. Y., Hart, C. M. (2006). The Drosophila Boundary Element-Associated Factors BEAF-32A and BEAF-32B Affect Chromatin Structure. Genetics 173: 1365-1375 [Abstract] [Full Text]  
  • Choi, Y.-J., Choi, T.-Y., Yamaguchi, M., Matsukage, A., Kim, Y.-S., Yoo, M.-A. (2004). Transcriptional regulation of the Drosophila caudal homeobox gene by DRE/DREF. Nucleic Acids Res 32: 3734-3742 [Abstract] [Full Text]  
  • Kuhn, E. J., Hart, C. M., Geyer, P. K. (2004). Studies of the Role of the Drosophila scs and scs' Insulators in Defining Boundaries of a Chromosome Puff. Mol. Cell. Biol. 24: 1470-1480 [Abstract] [Full Text]  
  • Ohshima, N., Takahashi, M., Hirose, F. (2003). Identification of a Human Homologue of the DREF Transcription Factor with a Potential Role in Regulation of the Histone H1 Gene. J. Biol. Chem. 278: 22928-22938 [Abstract] [Full Text]  
  • Blanton, J., Gaszner, M., Schedl, P. (2003). Protein:protein interactions and the pairing of boundary elements in vivo. Genes Dev. 17: 664-675 [Abstract] [Full Text]  
  • Jaquet, Y., Delattre, M., Spierer, A., Spierer, P. (2002). Functional dissection of the Drosophila modifier of variegation Su(var)3-7. Development 129: 3975-3982 [Abstract] [Full Text]  
  • Hirose, F., Ohshima, N., Kwon, E.-J., Yoshida, H., Yamaguchi, M. (2002). Drosophila Mi-2 Negatively Regulates dDREF by Inhibiting Its DNA-Binding Activity. Mol. Cell. Biol. 22: 5182-5193 [Abstract] [Full Text]  
  • Hirose, F., Ohshima, N., Shiraki, M., Inoue, Y. H., Taguchi, O., Nishi, Y., Matsukage, A., Yamaguchi, M. (2001). Ectopic Expression of DREF Induces DNA Synthesis, Apoptosis, and Unusual Morphogenesis in the Drosophila Eye Imaginal Disc: Possible Interaction with Polycomb and trithorax Group Proteins. Mol. Cell. Biol. 21: 7231-7242 [Abstract] [Full Text]  
  • Bell, A. C., West, A. G., Felsenfeld, G. (2001). Insulators and Boundaries: Versatile Regulatory Elements in the Eukaryotic Genome. Science 291: 447-450 [Abstract] [Full Text]  
  • Vazquez, J., Schedl, P. (2000). Deletion of an Insulator Element by the Mutation facet-strawberry in Drosophila melanogaster. Genetics 155: 1297-1311 [Abstract] [Full Text]  
  • Hirose, F., Yamaguchi, M., Matsukage, A. (1999). Targeted Expression of the DNA Binding Domain of DRE-Binding Factor, a Drosophila Transcription Factor, Attenuates DNA Replication of the Salivary Gland and Eye Imaginal Disc. Mol. Cell. Biol. 19: 6020-6028 [Abstract] [Full Text]  
  • Gaszner, M., Vazquez, J., Schedl, P. (1999). The Zw5 protein, a component of the scs chromatin domain boundary, is able to block enhancer-promoter interaction. Genes Dev. 13: 2098-2107 [Abstract] [Full Text]  
  • Khosla, S., Aitchison, A., Gregory, R., Allen, N. D., Feil, R. (1999). Parental Allele-Specific Chromatin Configuration in a Boundary-Imprinting-Control Element Upstream of the Mouse H19 Gene. Mol. Cell. Biol. 19: 2556-2566 [Abstract] [Full Text]  
  • Cuvier, O., Hart, C. M., Laemmli, U. K. (1998). Identification of a Class of Chromatin Boundary Elements. Mol. Cell. Biol. 18: 7478-7486 [Abstract] [Full Text]  
  • Hayashi, Y., Hirose, F., Nishimoto, Y., Shiraki, M., Yamagishi, M., Matsukage, A., Yamaguchi, M. (1997). Identification of CFDD (Common Regulatory Factor for DNA Replication and DREF Genes) and Role of Its Binding Site in Regulation of the Proliferating Cell Nuclear Antigen Gene Promoter. J. Biol. Chem. 272: 22848-22858 [Abstract] [Full Text]