Incapacitating the evolutionary capacitor: Hsp90 modulation of disease

被引:29
|
作者
Yeyati, Patricia L. [1 ]
van Heyningen, Veronica [1 ]
机构
[1] Western Gen Hosp, MRC, Human Genet Unit, Edinburgh, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.gde.2008.07.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The nature-nurture argument surrounding the mechanisms of disease causation cannot be resolved, as the roles of genes and environment are inextricably entwined. Environmental fluctuation is clearly a major modifier of phenotype, as well as a promoter of evolutionary change. Both types of variability can be mediated by the stress response pathway, with the Hsp90 chaperone family as key components. Hsp90 has been hailed as a capacitor for evolutionary change, because partial inhibition of its functions can uncover cryptic mutations, leading to unexpected phenotypes that, although generally deleterious, will under rare new environmental conditions provide improved survival to the carrier of that variant. There is, therefore, a strong environmentally elicited link between the capacity to reveal hidden variation as human disease phenotype and as novel morphological forms for evolutionary selection.
引用
收藏
页码:264 / 272
页数:9
相关论文
共 50 条
  • [41] Interactions of eNOS with sGC in the eNOS/Hsp90/sGC complex are mediated by Hsp90
    Venema, RC
    Venema, VJ
    Ju, H
    Harris, MB
    Snead, C
    Dimitropoulou, C
    Catravas, JD
    FASEB JOURNAL, 2002, 16 (05): : A952 - A952
  • [42] Expression of HSP90α and HSP90β in the idiopathic inflammatory myopathies and Duchenne muscular dystrophy
    De Bleecker, J. L.
    De Paepe, B.
    Creus, K. K.
    Martin, J. J.
    Weis, J.
    NEUROMUSCULAR DISORDERS, 2009, 19 (8-9) : 653 - 653
  • [43] Role and regulation of heat shock proteins Hsp90α and Hsp90β in multiple Myeloma
    Jain, S.
    Bargou, R. C.
    KLINISCHE PADIATRIE, 2008, 220 (03): : 202 - 202
  • [44] HSP90α、HSP90β在人胃癌组织中的表达
    吴梦婕
    张红
    姚元春
    秦蓉
    安徽医科大学学报, 2014, 49 (12) : 1754 - 1758
  • [45] Interaction of cepharanthine with immobilized heat shock protein 90α (Hsp90α) and screening of Hsp90α inhibitors
    Haginaka, Jun
    Kitabatake, Tomoko
    Hirose, Iyo
    Matsunaga, Hisami
    Moaddel, Ruin
    ANALYTICAL BIOCHEMISTRY, 2013, 434 (01) : 202 - 206
  • [46] Synergistic role of HSP90α and HSP90β to promote myofibroblast persistence in lung fibrosis
    Bellaye, Pierre-Simon
    Shimbori, Chiko
    Yanagihara, Toyoshi
    Carlson, David A.
    Hughes, Philip
    Upagupta, Chandak
    Sato, Seidai
    Wheildon, Nolan
    Haystead, Timothy
    Ask, Kjetil
    Kolb, Martin
    EUROPEAN RESPIRATORY JOURNAL, 2018, 51 (02)
  • [47] Expressed as the sole Hsp90 of yeast, the α and β isoforms of human Hsp90 differ with regard to their capacities for activation of certain client proteins, whereas only Hsp90β generates sensitivity to the Hsp90 inhibitor radicicol
    Millson, Stefan H.
    Truman, Andrew W.
    Racz, Attila
    Hu, Bin
    Panaretou, Barry
    Nuttall, James
    Mollapour, Mehdi
    Soeti, Csaba
    Piper, Peter W.
    FEBS JOURNAL, 2007, 274 (17) : 4453 - 4463
  • [48] Alternate Strategies of Hsp90 Modulation for the Treatment of Cancer and Other Diseases
    Brandt, Gary E. L.
    Blagg, Brian S. J.
    CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2009, 9 (15) : 1447 - 1461
  • [49] Hsp90: Structure and Function
    Jackson, Sophie E.
    MOLECULAR CHAPERONES, 2013, 328 : 155 - 240
  • [50] Hsp90: Twist and fold
    Richter, Klaus
    Buchner, Johannes
    CELL, 2006, 127 (02) : 251 - 253