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 Mitchell, P J
Right arrow Articles by Chasin, L A
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mitchell, P J
Right arrow Articles by Chasin, L A

 Previous Article  |  Next Article 

Mol Cell Biol. 1986 February; 6(2): 425-440

Multiple transcription start sites, DNase I-hypersensitive sites, and an opposite-strand exon in the 5' region of the CHO dhfr gene.

P J Mitchell, A M Carothers, J H Han, J D Harding, E Kas, L Venolia and L A Chasin

ABSTRACT

Transcription of the 26-kilobase (kb) dihydrofolate reductase (dhfr) gene in CHO cells is initiated at two sites: a major site (approximately 85% of the dhfr mRNA) at -63 relative to the translation start and a minor site (approximately 15%) at -107. Transcription also occurs from the opposite DNA strand in the dhfr 5' region, with a probable initiation site at approximately -195 relative to the dhfr translation start. A 4-kb polyadenylated RNA that is derived from the opposite-strand transcription increases threefold in abundance after serum starvation of CHO cells for 24 h. dhfr mRNA levels do not change during this time. The first dhfr exon lies within a 1-kb genomic region marked by exceptionally high G + C content and lack of DNA methylation. This region also includes a 214-base-pair (bp) exon for the opposite-strand transcript and five of the six DNase I-hypersensitive sites identified at the dhfr locus. Analysis of the DNA sequences of hamster, human (M. Chen, T. Shimada, A. D. Moulton, A. Cline, R. K. Humphries, J. Maizel, and A. W. Nienhuis, J. Biol. Chem. 259:3933-3943, 1984), and mouse (M. McGrogan, C. C. Simonsen, D. T. Smouse, P. J. Farnham, and R. T. Schimke, J. Biol. Chem. 260:2307-2314, 1985) dhfr genes reveals the presence of a 29-bp unit that is conserved 45 to 49 bp upstream of major and minor dhfr transcription start sites. This unit follows the consensus: GRGGCGGTGGCCTNNNNTGTCRCAARTRGGTR. The 5' part of the 29-bp unit contains a GC box that agrees with the GGGCGG consensus-binding site for the RNA polymerase II transcription factor Sp1 (D. Gidoni, W. A. Dynan, and R. Tjian, Nature (London) 312:409-413, 1984). Each of the three mammalian dhfr genes has several G-rich GC boxes proximal to the major dhfr transcription start site and several GC boxes of the opposite orientation (C rich) in a distal region about 500 bp upstream.


Mol Cell Biol. 1986 February; 6(2): 425-440




This article has been cited by other articles:

  • Dimitrova, D. S. (2006). Nuclear transcription is essential for specification of mammalian replication origins.. GENES CELLS 11: 829-844 [Abstract] [Full Text]  
  • Sasaki, T., Ramanathan, S., Okuno, Y., Kumagai, C., Shaikh, S. S., Gilbert, D. M. (2006). The Chinese Hamster Dihydrofolate Reductase Replication Origin Decision Point Follows Activation of Transcription and Suppresses Initiation of Replication within Transcription Units. Mol. Cell. Biol. 26: 1051-1062 [Abstract] [Full Text]  
  • Feng, Z., Hu, W., Chasin, L. A., Tang, M.-s. (2003). Effects of genomic context and chromatin structure on transcription-coupled and global genomic repair in mammalian cells. Nucleic Acids Res 31: 5897-5906 [Abstract] [Full Text]  
  • Hu, W., Feng, Z., Chasin, L. A., Tang, M.-s. (2002). Transcription-coupled and Transcription-independent Repair of Cyclobutane Pyrimidine Dimers in the Dihydrofolate Reductase Gene. J. Biol. Chem. 277: 38305-38310 [Abstract] [Full Text]  
  • Silberstein, E., Dveksler, G., Kaplan, G. G. (2001). Neutralization of Hepatitis A Virus (HAV) by an Immunoadhesin Containing the Cysteine-Rich Region of HAV Cellular Receptor-1. J. Virol. 75: 717-725 [Abstract] [Full Text]  
  • Noe, V., Ciudad, C. J., Chasin, L. A. (1999). Effect of Differential Polyadenylation and Cell Growth Phase on Dihydrofolate Reductase mRNA Stability. J. Biol. Chem. 274: 27807-27814 [Abstract] [Full Text]  
  • Bergsma, D J, Ai, Y, Skach, W R, Nesburn, K, Anoia, E, Van Horn, S, Stambolian, D (1996). Fine structure of the human galactokinase GALK1 gene.. Genome Res 6: 980-985 [Abstract]  
  • Nicol, L, Jeppesen, P (1996). Chromatin organization in the homogeneously staining regions of a methotrexate-resistant mouse cell line: interspersion of inactive and active chromatin domains distinguished by acetylation of histone H4. J. Cell Sci. 109: 2221-2228 [Abstract]  
  • Wade, M., Blake, M. C., Jambou, R. C., Helin, K., Harlow, E., Azizkhan, J. C. (1995). An Inverted Repeat Motif Stabilizes Binding of E2F and Enhances Transcription of the Dihydrofolate Reductase Gene. J. Biol. Chem. 270: 9783-9791 [Abstract] [Full Text]  
  • Trimble, J., Murthy, S., Bakker, A, Grassmann, R, Desrosiers, R. (1988). A gene for dihydrofolate reductase in a herpesvirus. Science 239: 1145-1147 [Abstract]