Regulatory functions of FKBP5 intronic regions associated with psychiatric disorders

被引:14
|
作者
Mendonca, Mariana S. [1 ]
Mangiavacchi, Paula M. [2 ]
Rios, Alvaro F. L. [1 ]
机构
[1] North Fluminense State Univ, Ctr Biosci & Biotechnol CBB, Lab Biotechnol LBT, Rio De Janeiro, Brazil
[2] North Fluminense State Univ, Lab Reprod & Anim Breeding LRMGA, Ctr Agr Technol Sci CCTA, Rio De Janeiro, Brazil
关键词
HPA axis; FKBP5; Intronic SNP; DNA methylation; Major depressive disorder; Post-traumatic stress disorder; INTRAGENIC DNA METHYLATION; GLUCOCORTICOID-RECEPTOR; CHILDHOOD MALTREATMENT; LIFE EVENTS; GENE; STRESS; DEPRESSION; POLYMORPHISM; BRAIN; MECHANISM;
D O I
10.1016/j.jpsychires.2021.08.014
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The FKBP5 gene codifies a co-chaperone protein associated with the modulation of glucocorticoid receptor interaction involved in the adaptive stress response. The FKBP5 intracellular concentration affects the binding affinity of the glucocorticoid receptor (GR) to glucocorticoids (GCs). This gene has glucocorticoid response elements (GREs) located in introns 2, 5 and 7, which affect its expression. Recent studies have examined GRE activity and the effects of genetic variants on transcript efficiency and their contribution to susceptibility to behavioral disorders. Epigenetic changes and environmental factors can influence the effects of these allelespecific variants, impacting the response to GCs of the FKBP5 gene. The main epigenetic mark investigated in FKBP5 intronic regions is DNA methylation, however, few studies have been performed for all GREs located in these regions. One of the major findings was the association of low DNA methylation levels in the intron 7 of FKBP5 in patients with psychiatric disorders. To date, there are no reports of DNA methylation in introns 2 and 5 of the gene associated with diagnoses of psychiatric disorders. This review highlights what has been discovered so far about the relationship between polymorphisms and epigenetic targets in intragenic regions, and reveals the gaps that need to be explored, mainly concerning the role of DNA methylation in these regions and how it acts in psychiatric disease susceptibility.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 50 条
  • [21] Adverse Childhood Experiences and Methylation of the FKBP5 Gene in Patients with Psychotic Disorders
    Misiak, Blazej
    Karpinski, Pawel
    Szmida, Elzbieta
    Grazlewski, Tomasz
    Jablonski, Marcin
    Cyranka, Katarzyna
    Rymaszewska, Joanna
    Piotrowski, Patryk
    Kotowicz, Kamila
    Frydecka, Dorota
    JOURNAL OF CLINICAL MEDICINE, 2020, 9 (12) : 1 - 15
  • [22] FKBP5, a depression-associated gene, mediates autophagy initiation
    Park, H.
    Jung, S. -Y.
    Chang, J.
    Lee, S.
    MOLECULAR BIOLOGY OF THE CELL, 2023, 34 (02) : 337 - 337
  • [23] Polymorphisms in FKBP5 are associated with peritraumatic dissociation in medically injured children
    Koenen, KC
    Saxe, G
    Purcell, S
    Smoller, JW
    Bartholomew, D
    Miller, A
    Hall, E
    Kaplow, J
    Bosquet, M
    Moulton, S
    Baldwin, C
    MOLECULAR PSYCHIATRY, 2005, 10 (12) : 1058 - 1059
  • [24] Correspondence: FKBP5 blockade may provide a new horizon for the treatment of stress-associated disorders: An in silico study
    Shang, Xiang
    Sun, Xiaoming
    Pan, Shuman
    EPILEPSIA OPEN, 2023, 8 (04) : 1628 - 1629
  • [25] The association of FKBP5 polymorphisms with the severity of depressive disorder in patients with methamphetamine use disorders
    Fang, Ting
    Liu, Meng-Nan
    Tian, Xiao-Yu
    Lu, Guan-Yi
    Li, Fei
    Zhang, Xiaojie
    Liu, Feng
    Hao, Wei
    Wu, Ning
    Li, Hong
    Li, Jin
    FRONTIERS IN PSYCHIATRY, 2023, 14
  • [26] Effects of Psychiatric Disease and Aging on FKBP5/1 Expression are Specific to Cortical Supragranular Neurons
    Matosin, Natalie
    Czamara, Darina
    Knauer-Arloth, Janine
    Mechawar, Naguib
    Dean, Brian
    Turecki, Gustavo
    Hyde, Thomas
    Binder, Elisabeth
    NEUROPSYCHOPHARMACOLOGY, 2022, 47 : 339 - 339
  • [27] Associations of psychiatric disease and ageing with FKBP5 expression converge on superficial layer neurons of the neocortex
    Natalie Matosin
    Janine Arloth
    Darina Czamara
    Katrina Z. Edmond
    Malosree Maitra
    Anna S. Fröhlich
    Silvia Martinelli
    Dominic Kaul
    Rachael Bartlett
    Amber R. Curry
    Nils C. Gassen
    Kathrin Hafner
    Nikola S. Müller
    Karolina Worf
    Ghalia Rehawi
    Corina Nagy
    Thorhildur Halldorsdottir
    Cristiana Cruceanu
    Miriam Gagliardi
    Nathalie Gerstner
    Maik Ködel
    Vanessa Murek
    Michael J. Ziller
    Elizabeth Scarr
    Ran Tao
    Andrew E. Jaffe
    Thomas Arzberger
    Peter Falkai
    Joel E. Kleinmann
    Daniel R. Weinberger
    Naguib Mechawar
    Andrea Schmitt
    Brian Dean
    Gustavo Turecki
    Thomas M. Hyde
    Elisabeth B. Binder
    Acta Neuropathologica, 2023, 145 : 439 - 459
  • [28] A FKBP5 mutation is associated with Paget’s disease of bone and enhances osteoclastogenesis
    Bingru Lu
    Yulian Jiao
    Yinchang Wang
    Jing Dong
    Muyun Wei
    Bin Cui
    Yafang Sun
    Laicheng Wang
    Bingchang Zhang
    Zijiang Chen
    Yueran Zhao
    Experimental & Molecular Medicine, 2017, 49 : e336 - e336
  • [29] A depression-associated protein FKBP5 functions in autophagy initiation through scaffolding the VPS34 complex
    Park, Hyungsun
    Park, Jisoo
    Kim, Taewan
    Heo, Hansol
    Chang, Jaerak
    Blackstone, Craig
    Lee, Seongju
    MOLECULAR NEUROBIOLOGY, 2025,
  • [30] A FKBP5 mutation is associated with Paget's disease of bone and enhances osteoclastogenesis
    Lu, Bingru
    Jiao, Yulian
    Wang, Yinchang
    Dong, Jing
    Wei, Muyun
    Cui, Bin
    Sun, Yafang
    Wang, Laicheng
    Zhang, Bingchang
    Chen, Zijiang
    Zhao, Yueran
    EXPERIMENTAL AND MOLECULAR MEDICINE, 2017, 49 : e336 - e336