2021
DOI: 10.1016/j.bbamcr.2021.119000
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Differential regulation of the glucocorticoid receptor nucleocytoplasmic shuttling by TPR-domain proteins

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Cited by 13 publications
(8 citation statements)
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“…For example, tetratricopeptide repeat (TPR) domains, which mediate protein-protein interactions ( Dermouche et al, 2021 ), Studies have shown that the C-terminal of Hsp90 dimer forms a functional receptor site for a co-partner carrying a tetratricopeptide repeat (TPR) domain, and they bind in a mutually exclusive or competitive manner. The biology of the glucocorticoid receptor (Hsp90•GR) complex is more potent, and it is a major player in the GR transport process ( Mazaira et al, 2021 ). Most MYB proteins act as transcription factors and have been shown to be involved in regulating various cellular processes, including cell cycle and morphogenesis, biological and abiotic stress responses ( Roy, 2016 ).…”
Section: Discussionmentioning
confidence: 99%
“…For example, tetratricopeptide repeat (TPR) domains, which mediate protein-protein interactions ( Dermouche et al, 2021 ), Studies have shown that the C-terminal of Hsp90 dimer forms a functional receptor site for a co-partner carrying a tetratricopeptide repeat (TPR) domain, and they bind in a mutually exclusive or competitive manner. The biology of the glucocorticoid receptor (Hsp90•GR) complex is more potent, and it is a major player in the GR transport process ( Mazaira et al, 2021 ). Most MYB proteins act as transcription factors and have been shown to be involved in regulating various cellular processes, including cell cycle and morphogenesis, biological and abiotic stress responses ( Roy, 2016 ).…”
Section: Discussionmentioning
confidence: 99%
“…Notably, all three of these co-chaperones can be in complex with the co-chaperone PP5 (Woodford et al, 2016(Woodford et al, , 2017, a protein phosphatase that dephosphorylates and inactivates GR (Wang et al, 2007;Zuo et al, 1999). The Hsp90 co-chaperones FKBP51 and -52 are also specialized SHR co-chaperones that regulate SHR maturation and play a role in translocation of ligand-bound SHR to the nucleus (Guy et al, 2015;Mazaira et al, 2021;Riggs et al, 2007). While it remains unknown whether FNIPs and Tsc1 are important for subcellular localization of SHR, the current understanding of SHR activation would suggest that all components of the complex present at the time of ligand binding localize to the nuclear membrane.…”
Section: Discussionmentioning
confidence: 99%
“…Another study observed high nuclear GR signal in dorsal CA1 and dentate gyrus only in rats that were strongly affected by predator scent exposure ( Danan et al, 2021 ). While the presence of GR nuclear generally follows corticosterone levels, additional regulatory mechanisms are governing nuclear translocation ( Mazaira et al, 2021 ), and these may be relevant to the brain as evidenced by the nuclear GR localization even in adrenalectomized rats ( Sarabdjitsingh et al, 2009 ). FKBP5 is an often studied factor in this respect, i.e., both target and regulator of GR function ( Binder, 2009 ; Matosin et al, 2018 ; Häusl et al, 2019 ).…”
Section: Discussionmentioning
confidence: 99%