Identification of a SIRT1 Mutation in a Family with Type 1 Diabetes

被引:97
作者
Biason-Lauber, Anna [1 ]
Boni-Schnetzler, Marianne [2 ,3 ]
Hubbard, Basil P. [4 ]
Bouzakri, Karim [5 ]
Brunner, Andrea [2 ,3 ]
Cavelti-Weder, Claudia [2 ,3 ]
Keller, Cornelia [2 ,3 ]
Meyer-Boni, Monika [1 ]
Meier, Daniel T. [2 ,3 ]
Brorsson, Caroline [6 ]
Timper, Katharina [2 ,3 ]
Leibowitz, Gil [7 ]
Patrignani, Andrea [8 ]
Bruggmann, Remy [8 ]
Boily, Gino [10 ]
Zulewski, Henryk [2 ,3 ]
Geier, Andreas [11 ]
Cermak, Jennifer M. [15 ]
Elliott, Peter [15 ]
Ellis, James L. [15 ]
Westphal, Christoph [15 ]
Knobel, Urs [2 ,3 ]
Eloranta, Jyrki J. [12 ]
Kerr-Conte, Julie [16 ]
Pattou, Francois [16 ]
Konrad, Daniel [17 ]
Matter, Christian M. [13 ,14 ]
Fontana, Adriano [9 ]
Rogler, Gerhard [11 ]
Schlapbach, Ralph [8 ]
Regairaz, Camille [18 ]
Carballido, Jose M. [18 ]
Glaser, Benjamin [7 ]
McBurney, Michael W. [10 ]
Pociot, Flemming [6 ]
Sinclair, David A. [4 ]
Donath, Marc Y. [2 ,3 ]
机构
[1] Univ Fribourg, Dept Med, CH-1700 Fribourg, Switzerland
[2] Univ Hosp Basel, Endocrinol Diabet & Metab, CH-4031 Basel, Switzerland
[3] Univ Basel Hosp, Dept Biomed, CH-4031 Basel, Switzerland
[4] Harvard Sch Med, Paul F Glenn Labs Biol Mech Aging, Dept Genet, Boston, MA 02115 USA
[5] Univ Geneva, Univ Med Ctr, Dept Genet Med & Dev, CH-1211 Geneva, Switzerland
[6] Glostrup Univ Hosp, Glostrup Res Inst, DK-2600 Glostrup, Denmark
[7] Hadassah Hebrew Univ, Dept Med, Endocrinol & Metab Serv, Med Ctr, IL-91120 Jerusalem, Israel
[8] Univ Zurich, Fed Inst Technol, Funct Genom Ctr Zurich, CH-8057 Zurich, Switzerland
[9] Univ Zurich, Inst Expt Immunol, CH-8057 Zurich, Switzerland
[10] Univ Ottawa, Ottawa, ON K1H 8L6, Canada
[11] Ctr Integrat Human Physiol, Gastroenterol &Hepatol, CH-8091 Zurich, Switzerland
[12] Ctr Integrat Human Physiol, Dept Clin Pharmacol & Toxicol, CH-8091 Zurich, Switzerland
[13] Ctr Integrat Human Physiol, Dept Cardiol, CH-8091 Zurich, Switzerland
[14] Univ Zurich Hosp, CH-8091 Zurich, Switzerland
[15] Sirtris, Cambridge, MA 02139 USA
[16] Univ Lille Nord France, F-59045 Lille, France
[17] Univ Childrens Hosp, CH-8032 Zurich, Switzerland
[18] Novartis Inst BioMed Res, CH-4002 Basel, Switzerland
基金
加拿大自然科学与工程研究理事会; 瑞士国家科学基金会;
关键词
MAMMALIAN SIRTUINS; INSULIN-SECRETION; BETA-CELLS; PROTEIN; EXPRESSION; KINASE; ROLES;
D O I
10.1016/j.cmet.2013.02.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Type 1 diabetes is caused by autoimmune-mediated beta cell destruction leading to insulin deficiency. The histone deacetylase SIRT1 plays an essential role in modulating several age-related diseases. Here we describe a family carrying a mutation in the SIRT1 gene, in which all five affected members developed an autoimmune disorder: four developed type 1 diabetes, and one developed ulcerative colitis. Initially, a 26-year-old man was diagnosed with the typical features of type 1 diabetes, including lean body mass, autoantibodies, T cell reactivity to beta cell antigens, and a rapid dependence on insulin. Direct and exome sequencing identified the presence of a T-to-C exchange in exon 1 of SIRT1, corresponding to a leucine-to-proline mutation at residue 107. Expression of SIRT1-L107P in insulin-producing cells resulted in overproduction of nitric oxide, cytokines, and chemokines. These observations identify a role for SIRT1 in human autoimmunity and unveil a monogenic form of type 1 diabetes.
引用
收藏
页码:448 / 455
页数:8
相关论文
共 36 条
[1]   An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains [J].
Aaltonen, J ;
Bjorses, P ;
Perheentupa, J ;
HorelliKuitunen, N ;
Palotie, A ;
Peltonen, L ;
Lee, YS ;
Francis, F ;
Hennig, S ;
Thiel, C ;
Lehrach, H ;
Yaspo, ML .
NATURE GENETICS, 1997, 17 (04) :399-403
[3]   Human Sirt-1: Molecular Modeling and Structure-Function Relationships of an Unordered Protein [J].
Autiero, Ida ;
Costantini, Susan ;
Colonna, Giovanni .
PLOS ONE, 2009, 4 (10)
[4]   Modeling of the Bacterial Mechanism of Methicillin-Resistance by a Systems Biology Approach [J].
Autiero, Ida ;
Costantini, Susan ;
Colonna, Giovanni .
PLOS ONE, 2009, 4 (07)
[5]   SirT1 Gain of Function Increases Energy Efficiency and Prevents Diabetes in Mice [J].
Banks, Alexander S. ;
Kon, Ning ;
Knight, Colette ;
Matsumoto, Michihiro ;
Gutierrez-Juarez, Roger ;
Rossetti, Luciano ;
Gu, Wei ;
Accili, Domenico .
CELL METABOLISM, 2008, 8 (04) :333-341
[6]   Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes [J].
Barrett, Jeffrey C. ;
Clayton, David G. ;
Concannon, Patrick ;
Akolkar, Beena ;
Cooper, Jason D. ;
Erlich, Henry A. ;
Julier, Cecile ;
Morahan, Grant ;
Nerup, Jorn ;
Nierras, Concepcion ;
Plagnol, Vincent ;
Pociot, Flemming ;
Schuilenburg, Helen ;
Smyth, Deborah J. ;
Stevens, Helen ;
Todd, John A. ;
Walker, Neil M. ;
Rich, Stephen S. .
NATURE GENETICS, 2009, 41 (06) :703-707
[7]   Histone Deacetylases 6 and 9 and Sirtuin-1 Control Foxp3+ Regulatory T Cell Function Through Shared and Isoform-Specific Mechanisms [J].
Beier, Ulf H. ;
Wang, Liqing ;
Han, Rongxiang ;
Akimova, Tatiana ;
Liu, Yujie ;
Hancock, Wayne W. .
SCIENCE SIGNALING, 2012, 5 (229)
[8]   Sirtuin-1 Targeting Promotes Foxp3+ T-Regulatory Cell Function and Prolongs Allograft Survival [J].
Beier, Ulf H. ;
Wang, Liqing ;
Bhatti, Tricia R. ;
Liu, Yujie ;
Han, Rongxiang ;
Ge, Guanghui ;
Hancock, Wayne W. .
MOLECULAR AND CELLULAR BIOLOGY, 2011, 31 (05) :1022-1029
[9]   The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3 [J].
Bennett, CL ;
Christie, J ;
Ramsdell, F ;
Brunkow, ME ;
Ferguson, PJ ;
Whitesell, L ;
Kelly, TE ;
Saulsbury, FT ;
Chance, PF ;
Ochs, HD .
NATURE GENETICS, 2001, 27 (01) :20-21
[10]   Sirt1 regulates insulin secretion by repressing UCP2 in pancreatic β cells [J].
Bordone, L ;
Motta, MC ;
Picard, F ;
Robinson, A ;
Jhala, US ;
Apfeld, J ;
McDonagh, T ;
Lemieux, M ;
McBurney, M ;
Szilvasi, A ;
Easlon, EJ ;
Lin, SJ ;
Guarente, L .
PLOS BIOLOGY, 2006, 4 (02) :210-220