The mitochondrial rhomboid protease PSARL is a new candidate gene for type 2 diabetes
Open accessAbstract
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.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
PARL polymorphisms in humans are associated with insulin resistance.
“Moreover, polymorphisms of PARL in humans are associated with insulin resistance (325).”
From Mitochondrial Dysfunction in Diabetes: From Molecular Mechanisms to Functional Significance and Therapeutic Opportunities (2010) · cites this paper as [325]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
The citation lists haven’t been fetched yet
References 43 · Cited by 85
- Authors
- 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, G. R.
- Affiliations
- Deakin University (AU)
- Pennington Biomedical Research Center (US)
- The University of Texas at San Antonio Health Science Center (US)
- Texas Biomedical Research Institute (US)
- Medical College of Wisconsin (US)
- Corresponding author
- Walder, K.
- Venue
- Diabetologia
- Published
- 2005-02-24
- Volume
- 48
- Issue
- 3
- Pages
- 459-468
- ISSN
- 0012-186X (ISSN-L)
- 1432-0428
- OpenAlex
- W2011777452
- Cited by
- 85
- References
- 43
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 2 · 2021: 1 · 2020: 2 · 2019: 2 · 2018: 9 · 2017: 5 · 2016: 6 · 2015: 2 · 2014: 6 · 2013: 8 · 2012: 3
- FWCI
- 2.39
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Diabetologia (publishedVersion)
- PubMed (publishedVersion)
- Own your potential (DEAKIN) (submittedVersion)
- Figshare (submittedVersion)
- Funders
- Deakin University
- National Institutes of Health (5r01hl034989-08, MH 59490, RR00058)
- Takeda Oncology
- National Heart, Lung, and Blood Institute (HL 34989)
- National Institute of Mental Health (MH59490)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK054026, DK-54026)
- National Center for Research Resources (RR00058, M01RR000058)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Keywords
- rhomboid protease, type 2 diabetes, insulin resistance, skeletal muscle, mitochondrial proteolysis, Psammomys obesus, exercise training, hyperinsulinemic-euglycemic clamp, plasma insulin, age, genetic risk factors, metabolic syndrome
- MeSH terms
- Amino Acid Sequence, Animals, Diabetes Mellitus, Type 2, Disease Models, Animal, Family, Female, Gerbillinae, Humans, Male, Mitochondria, Molecular Sequence Data, Sequence Alignment, Conserved Sequence, Sequence Homology, Amino Acid, Mitochondrial Proteins, Siblings, Metalloproteases
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review