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The human growth hormone gene contains both positive and negative control elements
L N Peritz1, E J Fodor, D W Silversides
1Metabolic Research Unit, University of California, San Francisco 94143.
The Journal of Biological Chemistry
|April 15, 1988
Summary
Researchers identified regulatory DNA elements in the human growth hormone (hGH) gene. These elements, I and II, modulate gene expression, with element II alone activating it, revealing shared regulatory mechanisms with adenovirus promoters.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
Background:
- The 5'-flanking region of the human growth hormone (hGH) gene contains regulatory sequences controlling its expression.
- Understanding these sequences is crucial for deciphering gene regulation mechanisms.
Purpose of the Study:
- To investigate protein-DNA interactions and functional roles of cis-acting elements in the hGH gene's 5'-flanking region.
- To identify transcription factors that bind to these regulatory elements and their impact on gene expression.
Main Methods:
- Protein-DNA binding assays were employed to detect factor interactions with hGH DNA.
- Gene transfer and expression experiments in HeLa cells were used to assess the functional impact of identified elements.
Main Results:
- Two adjacent cis-acting elements (I and II) located between nucleotides -308/-235 of the hGH gene were identified.
- Elements I and II repressed reporter gene expression, while element II alone demonstrated activation.
- Two distinct factors (Factor I and Factor II) were found to bind hGH DNA; Factor I binds single-stranded DNA and is linked to repression, while Factor II binds a region homologous to the adenovirus major late transcription factor binding site.
Conclusions:
- The hGH gene promoter contains regulatory elements that modulate its expression.
- A shared transcription regulatory element exists between the hGH and adenovirus major late promoters, involving Factor II binding.
- These findings provide insights into the complex regulation of hGH gene expression and potential cross-talk with viral gene regulation pathways.