Literature DB >> 2987264

Transcriptional regulation of mouse dihydrofolate reductase in the cell cycle.

P J Farnham, R T Schimke.   

Abstract

We have studied transcription of the dihydrofolate reductase gene as cells progress through the cell cycle. We used the techniques of DNA-excess filter hybridization and in vivo pulse labeling of a synchronous population of cells to measure the transcription rate of the dihydrofolate reductase gene in different phases of the cell cycle. Our results indicate that the dihydrofolate reductase gene is cell cycle regulated at the transcriptional level. The transcription rate is low in G1, increases 7-fold at the beginning of S phase, decreases almost immediately thereafter, and remains low throughout the remainder of S and into G2. This cell cycle regulation seen in the G1 to S phase transition is achieved by increasing the rate of transcription from a single promoter region. The fact that this region is similar to promoter regions of other housekeeping genes suggests that this type of regulation may not be unique to dihydrofolate reductase.

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Year:  1985        PMID: 2987264

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  49 in total

Review 1.  Integration of the pRB and p53 cell cycle control pathways.

Authors:  C L Stewart; A M Soria; P A Hamel
Journal:  J Neurooncol       Date:  2001-02       Impact factor: 4.130

2.  Molecular cloning and expression of the human deoxythymidylate kinase gene in yeast.

Authors:  J Y Su; R A Sclafani
Journal:  Nucleic Acids Res       Date:  1991-02-25       Impact factor: 16.971

Review 3.  Cell cycle control of DNA synthesis in budding yeast.

Authors:  L H Johnston; N F Lowndes
Journal:  Nucleic Acids Res       Date:  1992-05-25       Impact factor: 16.971

4.  Molecular organization of the human Raf-1 promoter region.

Authors:  T W Beck; U Brennscheidt; G Sithanandam; J Cleveland; U R Rapp
Journal:  Mol Cell Biol       Date:  1990-07       Impact factor: 4.272

5.  The cell cycle-coupled expression of topoisomerase IIalpha during S phase is regulated by mRNA stability and is disrupted by heat shock or ionizing radiation.

Authors:  P C Goswami; J L Roti Roti; C R Hunt
Journal:  Mol Cell Biol       Date:  1996-04       Impact factor: 4.272

6.  Transcription initiation from the dihydrofolate reductase promoter is positioned by HIP1 binding at the initiation site.

Authors:  A L Means; P J Farnham
Journal:  Mol Cell Biol       Date:  1990-02       Impact factor: 4.272

7.  Regulation of 4F2 heavy-chain gene expression during normal human T-cell activation can be mediated by multiple distinct molecular mechanisms.

Authors:  T Lindsten; C H June; C B Thompson; J M Leiden
Journal:  Mol Cell Biol       Date:  1988-09       Impact factor: 4.272

8.  The HIP1 binding site is required for growth regulation of the dihydrofolate reductase gene promoter.

Authors:  A L Means; J E Slansky; S L McMahon; M W Knuth; P J Farnham
Journal:  Mol Cell Biol       Date:  1992-03       Impact factor: 4.272

9.  Growth-rate-dependent regulation of the expression and inactivation of thymidylate synthase in Saccharomyces cerevisiae.

Authors:  M T Greenwood; E M Calmels; R K Storms
Journal:  J Bacteriol       Date:  1986-12       Impact factor: 3.490

10.  Murine dihydrofolate reductase transcripts through the cell cycle.

Authors:  P J Farnham; R T Schimke
Journal:  Mol Cell Biol       Date:  1986-02       Impact factor: 4.272

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