FK506-binding Proteins 51 and 52 Differentially Regulate Dynein Interaction and Nuclear Translocation of the Glucocorticoid Receptor in Mammalian Cells
Max Planck Society · Max Planck Institute of Psychiatry
Abstract
We used a cellular system to elucidate the molecular determinants of the large immunophilin FK506-binding proteins (FKBP)51 and -52 for their action on the glucocorticoid receptor in mammalian cells. Increasing the levels of FKBP51 reduced the transcriptional activity of the receptor, as reported. Elevated levels of FKBP52 per se showed no effect but mitigated the inhibition of the receptor induced by FKBP51. We discovered that nuclear translocation of the glucocorticoid receptor was delayed by FKBP51. This correlates with the reduced interaction of FKBP51 with the motor protein dynein compared with FKBP52. From mutational analyses, we concluded that three features of the immunophilins are required for…
Citation impact
- FWCI
- 7.20
- Percentile
- 100%
- References
- 52
Authors
6- GMGabriela M. WochnikCorresponding
Max Planck Society, Max Planck Institute of Psychiatry
- JRJoëlle Rüegg
Max Planck Institute of Psychiatry
- GAG. Abel
Max Planck Society, Max Planck Institute of Psychiatry
- USUlrike Schmidt
Max Planck Society, Max Planck Institute of Psychiatry
- FHFlorian Holsboer
Max Planck Society, Max Planck Institute of Psychiatry
Topics & keywords
- Chromosomal translocation
- Glucocorticoid receptor
- Cell biology
- Nuclear receptor
- Glucocorticoid
- Cell nucleus
- Nuclear protein
- Biology