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PIT-1 Protein Localization at Different Optical Sections in a Single Living Cell Using FRET Microscopy and Green Fluorescent Proteins

Published online by Cambridge University Press:  02 July 2020

Ammasi Periasamy
Affiliation:
Department of Biology, Advanced Cellular Imaging Facility (ACIF), Gilmer Hall University of Virginia, Charlottesville, VA22903
Richard N. Day
Affiliation:
Departments of Medicine and Cell Biology, NSF Center for Biological Timing, University of Virginia, Charlottesville, VA22908
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Extract

The pituitary specific transcription factor Pit-1 is required for transcriptional activity of the prolactin (PRL) gene. The Pit-1 protein is a member of the POU homeodomain transcription factors that is expressed in several different anterior pituitary cell types, where it functions as an important determinant of pituitary-specific gene expression. The Pit-1 protein generally interacts with DNA elements in the PRL gene promoter as a dimer, and has been demonstrated to associate with other transcription factors. The objective of our research is to define the critical molecular events involved in transcriptional regulation of the PRL gene in living cells. Methods that allow monitoring of the intimate interactions between protein partners in living cells provide an unparalleled perspective on these biological processes. Using the jellyfish green fluorescent protein (GFP) as a tag, we applied the fluorescence resonance energy transfer (FRET) technique to visualize where and when the Pit-1 protein interacts in the living cell. FRET is a quantum mechanical effect that occurs between donor (D) and acceptor (A) fluorophores provided: (i) the emission energy of D is coincident with the energy required to excite A, and (ii) the distance that separating the two fluorophores is 10-100 Å. Mutant forms of GFP that fluoresce either green or blue (BFP) have excitation and emission spectra that are suitable for FRET imaging.

Type
Cell Biology Applications of Green Fluorescent Protein and Other Vital Labeling Probes
Copyright
Copyright © Microscopy Society of America 1997

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References

1.Anderson, B. and Rosenfeld, M.G. (1994) J. Biol. Chem. 269: 2933529338Google Scholar
2.Holloway, J.M., et al., (1995) Genes Dev. 9:19922006.10.1101/gad.9.16.1992CrossRefGoogle Scholar
3.Bradford, A.P., et al., (1995) Mol. Cell. Biol. 15:28492857.10.1128/MCB.15.5.2849CrossRefGoogle Scholar
4.Herman, B. (1989) Methods Cell Biol. 30:216243.Google Scholar
5.This work was supported by awards from the Academic Enhancement Program of the University of Virginia (AP), the NSF DIR-8920162 Center for Biological Timing Technology Development sub-project (RND) and NIH RO1 -DK-43701 (RND).Google Scholar