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Imaging Analysis of Subcellular Correlation of Androgen Receptor and Estrogen Receptor α in Single Living Cells Using Green Fluorescent Protein Color Variants
Author(s) -
Ikuo Ochiai,
Kenichi Matsuda,
Mayumi Nishi,
Hitoshi Ozawa,
Mitsuhiro Kawata
Publication year - 2003
Publication title -
molecular endocrinology
Language(s) - English
Resource type - Journals
eISSN - 1944-9917
pISSN - 0888-8809
DOI - 10.1210/me.2002-0262
Subject(s) - biology , androgen receptor , estrogen receptor , subcellular localization , fluorescence , green fluorescent protein , receptor , androgen , microbiology and biotechnology , endocrinology , gene , biochemistry , genetics , breast cancer , cancer , prostate cancer , cytoplasm , hormone , physics , quantum mechanics
Androgen and estrogen act not only in a sex-specific manner but also interactively and synergistically. In the present study, to examine the possible interaction between androgen receptor (AR) and estrogen receptor-alpha (ERalpha), we investigated the subcellular dynamics of AR and ERalpha fused with green fluorescent protein color variants in single living cells using time-lapse microscopy and the technique of fluorescence recovery after photobleaching. AR and ERalpha showed punctate colocalization in the nucleus with estrogen, but not androgen. N-terminal AR deletion mutant did not form a nuclear punctate pattern with either androgen or estrogen. In the presence of AR, but not ERalpha, N-terminal AR deletion mutant formed a punctate nuclear pattern with androgen. AR had different mobility depending on the ligand and the presence of ERalpha. On the other hand, AR had little effect on the stability of ERalpha. ERalpha mutant that does not bind coactivators did not alter the mobility of AR. Taken together, using an imaging technique, we clarified that possible homo/hetero dimerization between AR and ERalpha could be attributed to androgen-estrogen interaction in living cells.

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