Persistent Synchronized Oscillations in Prolactin Gene Promoter Activity in Living Pituitary Cells1
PRL gene expression in the anterior pituitary gland responds rapidly to different hormonal signals. We have investigated the long-term timing of transcriptional activation from the PRL, GH, and cytomegalovirus promoters in response to different stimulus duration, using real-time imaging of luciferas...
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Published in | Endocrinology (Philadelphia) Vol. 142; no. 7; pp. 3255 - 3260 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English Japanese |
Published |
Endocrine Society
01.07.2001
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Online Access | Get full text |
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Summary: | PRL gene expression in the anterior pituitary gland responds
rapidly to different hormonal signals. We have investigated the
long-term timing of transcriptional activation from the PRL, GH, and
cytomegalovirus promoters in response to different stimulus duration,
using real-time imaging of luciferase expression in living stably
transfected GH3 cells. Long-term stimulation of serum-starved cells
with 50% serum induced a homogeneous rise in PRL promoter activity,
with subsequent heterogeneous fluctuations in luciferase activity in
individual cells. When cells were subjected to a 2-h pulse of 50%
serum, followed by serum-free medium, there were long-term
(approximately 50 h) synchronized, homogeneous oscillations in PRL
promoter activity. This response was PRL-specific, because in GH3 cells
expressing luciferase from the GH or cytomegalovirus promoters, a serum
pulse elicited no oscillations in luciferase expression after an
initial transient response to serum. The PRL promoter may therefore be
a template for an unstable transcription complex subject to stochastic
regulation, allowing an oscillatory transcriptional response to
physiological signals. This suggests that precise timing and
coordination of cell responses to different signal-duration may
represent a novel mechanism for coordinating long-term dynamic changes
in transcription in cell populations. |
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ISSN: | 0013-7227 1945-7170 |
DOI: | 10.1210/endo.142.7.8252 |