Nucleic Acids Research, 1995, Vol. 23, No. 22 4649-4656
© 1995
Articles |
Regulation of mouse thymidylate synthaswe gene expression in growth-stimulsated cells: upstream S phase control elements are indistinguishable from the essential promoter elements
Departments of Molecular Genetics and Biochemistry and the Ohio State Biochemistry Program, The Ohio State University Columbus, OH 43210, USA
*To whom correspondence should be addressed
Received August 8, 1995. Accepted October 20, 1995.
Expression of the mammalian thymidylate synthase (TS) gene in growth-stimulated cells is closely coordinated with entry into S phase. Previous studies with transfected TS mlnigenes have shown that sequences upstream of the coding region as well as an intron in the transcribed region are both necessary for proper regulation of TS mRNA content in growthstimulated cells. The goal of the present study was to identify the upstream regulatory elements. Minigenes consisting of TS 5' flanking sequences linked to the TS coding region (interrupted by introns 1 and 2) were stably transfected into mouse 3T6 cells. Deletion and site-directed mutagenesis of the 55' flanking region revealed that there is a close correspondence between the upstream sequences that are necessary for S phase regulation and the 30 nucleotide region that is essential for promoter activity. These observations raised the possibility that regulation of the TS gene occurs at the transcriptlonal level. However, nuclear run-on assays showed that the rate of transcription of the TS gene changed very little during the G1-S phase transition. Furthermore, when the TS promoter was linked to an intron-less luciferase indicator gene, there was no change in expression following growth-stimulation. Therefore it appears that the TS gene is controlled primarily at the posttranscriptional level, and that the TS essential promoter region is necessary (although not sufficient) for proper S phase regulation.
+Present address: Department of Cell Biology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 770303498, USA
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
V. Wilhelmi, C. O. Simon, J. Podlech, V. Bohm, T. Daubner, S. Emde, D. Strand, A. Renzaho, N. A. W. Lemmermann, C. K. Seckert, et al. Transactivation of Cellular Genes Involved in Nucleotide Metabolism by the Regulatory IE1 Protein of Murine Cytomegalovirus Is Not Critical for Viral Replicative Fitness in Quiescent Cells and Host Tissues J. Virol., October 15, 2008; 82(20): 9900 - 9916. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. O. Simon, R. Holtappels, H.-M. Tervo, V. Bohm, T. Daubner, S. A. Oehrlein-Karpi, B. Kuhnapfel, A. Renzaho, D. Strand, J. Podlech, et al. CD8 T Cells Control Cytomegalovirus Latency by Epitope-Specific Sensing of Transcriptional Reactivation J. Virol., November 1, 2006; 80(21): 10436 - 10456. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Gribaudo, L. Riera, T. L. Rudge, P. Caposio, L. F. Johnson, and S. Landolfo Human cytomegalovirus infection induces cellular thymidylate synthase gene expression in quiescent fibroblasts J. Gen. Virol., December 1, 2002; 83(12): 2983 - 2993. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Huang, M. Jokela, J. Tuusa, S. Skog, K. Poikonen, and J. E. Syvaoja E2F mediates induction of the Sp1-controlled promoter of the human DNA polymerase {{epsilon}} B-subunit gene POLE2 Nucleic Acids Res., July 1, 2001; 29(13): 2810 - 2821. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Gribaudo, L. Riera, D. Lembo, M. De Andrea, M. Gariglio, T. L. Rudge, L. F. Johnson, and S. Landolfo Murine Cytomegalovirus Stimulates Cellular Thymidylate Synthase Gene Expression in Quiescent Cells and Requires the Enzyme for Replication J. Virol., June 1, 2000; 74(11): 4979 - 4987. [Abstract] [Full Text] |
||||
![]() |
N. Horie and K. Takeishi Identification of Functional Elements in the Promoter Region of the Human Gene for Thymidylate Synthase and Nuclear Factors That Regulate the Expression of the Gene J. Biol. Chem., July 18, 1997; 272(29): 18375 - 18381. [Abstract] [Full Text] [PDF] |
||||



