Enhancers could, in principle, function by increasing the rate of reinitiation on individual adjacent active promoters or by increasing the probability that an adjacent promoter is activated for transcription. We have addressed this issue for the repetitive metazoan rDNA enhancer by microinjecting Xenopus oocytes with enhancer-less and enhancer-bearing genes and determining by EM the frequency that each gene type forms active transcription units and their transcript density. We use conditions where transcription requires the normal rDNA promoter and is stimulated 30-50-fold by the enhancer. (In contrast, at saturating template conditions as used in previous EM studies, an aberrant mode of transcription is activated that is not affected by the rDNA enhancer or by the generally recognized rDNA promoter). The active transcription units on enhancer-less genes are found to be as densely packed with nascent transcripts and polymerases as those on enhancer-bearing genes and on the endogenous rRNA genes. Significantly, the enhancer-bearing genes are approximately 30-50-fold more likely to form such active transcription units than enhancer-less genes, consistent with their amounts of transcript. Complementary studies confirm that the enhancer does not affect elongation rate, the stability of the transcription complex, or transcript half-life. These data demonstrate that the repetitive metazoan rDNA enhancer causes more genes to be actively transcribed and does not alter the reinitiation rate on individual active genes.
Skip Nav Destination
Article navigation
1 June 1996
Article|
June 01 1996
Metazoan rDNA enhancer acts by making more genes transcriptionally active.
Y N Osheim,
Y N Osheim
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
Search for other works by this author on:
E B Mougey,
E B Mougey
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
Search for other works by this author on:
J Windle,
J Windle
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
Search for other works by this author on:
M Anderson,
M Anderson
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
Search for other works by this author on:
M O'Reilly,
M O'Reilly
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
Search for other works by this author on:
O L Miller, Jr,
O L Miller, Jr
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
Search for other works by this author on:
A Beyer,
A Beyer
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
Search for other works by this author on:
B Sollner-Webb
B Sollner-Webb
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
Search for other works by this author on:
Y N Osheim
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
E B Mougey
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
J Windle
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
M Anderson
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
M O'Reilly
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
O L Miller, Jr
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
A Beyer
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
B Sollner-Webb
Department of Microbiology, University of Virginia School of Medicine, Charlottesville, 22908, USA.
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1996) 133 (5): 943–954.
Citation
Y N Osheim, E B Mougey, J Windle, M Anderson, M O'Reilly, O L Miller, A Beyer, B Sollner-Webb; Metazoan rDNA enhancer acts by making more genes transcriptionally active.. J Cell Biol 1 June 1996; 133 (5): 943–954. doi: https://doi.org/10.1083/jcb.133.5.943
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement
Advertisement