The mitochondrial rhomboid protease PSARL is a new candidate gene for type 2 diabetes

被引:69
作者
Walder, K
Kerr-Bayles, L
Civitarese, A
Jowett, J
Curran, J
Elliott, K
Trevaskis, J
Bishara, N
Zimmet, P
Mandarino, L
Ravussin, E
Blangero, J
Kissebah, A
Collier, GR
机构
[1] Deakin Univ, Sch Hlth Sci, Metab Res Unit, Waurn Ponds 3217, Australia
[2] Med Coll Wisconsin, Take Off Pounds Sensibly, Ctr Obes & Metab Res, Milwaukee, WI 53226 USA
[3] SW Fdn Biomed Res, San Antonio, TX 78284 USA
[4] Univ Texas, Hlth Sci Ctr, Dept Med, Div Diabet, San Antonio, TX 78284 USA
[5] Int Diabet Inst, Caulfield, Australia
[6] Pennington Biomed Res Ctr, Baton Rouge, LA USA
[7] ChemGenex Pharmaceut, Geelong, Vic, Australia
关键词
association; gene-oenvironment interaction; gene expression; Psammomys obesus;
D O I
10.1007/s00125-005-1675-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis: This study aimed to identify genes that are expressed in skeletal muscle, encode proteins with functional significance in mitochondria, and are associated with type 2 diabetes. Methods: We screened for differentially expressed genes in skeletal muscle of Psammomys obesus (Israeli sand rats), and prioritised these on the basis of genomic localisation and bioinformatics analysis for proteins with likely mitochondrial functions. Results: We identified a mitochondrial intramembrane protease, known as presenilins-associated rhomboid-like protein (PSARL) that is associated with insulin resistance and type 2 diabetes. Expression of PSARL was reduced in skeletal muscle of diabetic Psammomys obesus, and restored after exercise training to successfully treat the diabetes. PSARL gene expression in human skeletal muscle was correlated with insulin sensitivity as assessed by glucose disposal during a hyperinsulinaemic-euglycaemic clamp. In 1,031 human subjects, an amino acid substitution (Leu262Val) in PSARL was associated with increased plasma insulin concentration, a key risk factor for diabetes. Furthermore, this variant interacted strongly with age to affect insulin levels, accounting for 5% of the variation in plasma insulin in elderly subjects. Conclusions/interpretation: Variation in PSARL sequence and/or expression may be an important new risk factor for type 2 diabetes and other components of the metabolic syndrome.
引用
收藏
页码:459 / 468
页数:10
相关论文
共 43 条
  • [21] Linkage for BMI at 3q27 region confirmed in an African-American population
    Luke, A
    Wu, XD
    Zhu, XF
    Kan, DH
    Su, Y
    Cooper, R
    [J]. DIABETES, 2003, 52 (05) : 1284 - 1287
  • [22] Mitochondrial membrane remodelling regulated by a conserved rhomboid protease
    McQuibban, GA
    Saurya, S
    Freeman, M
    [J]. NATURE, 2003, 423 (6939) : 537 - 541
  • [23] PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes
    Mootha, VK
    Lindgren, CM
    Eriksson, KF
    Subramanian, A
    Sihag, S
    Lehar, J
    Puigserver, P
    Carlsson, E
    Ridderstråle, M
    Laurila, E
    Houstis, N
    Daly, MJ
    Patterson, N
    Mesirov, JP
    Golub, TR
    Tamayo, P
    Spiegelman, B
    Lander, ES
    Hirschhorn, JN
    Altshuler, D
    Groop, LC
    [J]. NATURE GENETICS, 2003, 34 (03) : 267 - 273
  • [24] Genome-wide search for type 2 diabetes in Japanese affected sib-pails confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate loci on 7p and 11p
    Mori, Y
    Otabe, S
    Dina, C
    Yasuda, K
    Populaire, C
    Lecoeur, C
    Vatin, V
    Durand, E
    Hara, K
    Okada, T
    Tobe, K
    Boutin, P
    Kadowaki, T
    Froguel, P
    [J]. DIABETES, 2002, 51 (04) : 1247 - 1255
  • [25] Coordinated reduction of genes of oxidative metabolism in humans with insulin resistance and diabetes:: Potential role of PGC1 and NRF1
    Patti, ME
    Butte, AJ
    Crunkhorn, S
    Cusi, K
    Berria, R
    Kashyap, S
    Miyazaki, Y
    Kohane, I
    Costello, M
    Saccone, R
    Landaker, EJ
    Goldfine, AB
    Mun, E
    DeFronzo, R
    Finlayson, J
    Kahn, CR
    Mandarino, LJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (14) : 8466 - 8471
  • [26] Pellegrini L, 2001, J ALZHEIMERS DIS, V3, P181
  • [27] Mitochondrial dysfunction in the elderly: Possible role in insulin resistance
    Petersen, KF
    Befroy, D
    Dufour, S
    Dziura, J
    Ariyan, C
    Rothman, DL
    DiPietro, L
    Cline, GW
    Shulman, GI
    [J]. SCIENCE, 2003, 300 (5622) : 1140 - 1142
  • [28] Effect of age on in vivo rates of mitochondrial protein synthesis in human skeletal muscle
    Rooyackers, OE
    Adey, DB
    Ades, PA
    Nair, KS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (26) : 15364 - 15369
  • [29] Markers of capacity to utilize fatty acids in human skeletal muscle: relation to insulin resistance and obesity and effects of weight loss
    Simoneau, JA
    Veerkamp, JH
    Turcotte, LP
    Kelley, DE
    [J]. FASEB JOURNAL, 1999, 13 (14) : 2051 - 2060
  • [30] SKELETAL-MUSCLE GLYCOLYTIC AND OXIDATIVE ENZYME CAPACITIES ARE DETERMINANTS OF INSULIN SENSITIVITY AND MUSCLE COMPOSITION IN OBESE WOMEN
    SIMONEAU, JA
    COLBERG, SR
    THAETE, FL
    KELLEY, DE
    [J]. FASEB JOURNAL, 1995, 9 (02) : 273 - 278