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Mol Cell Endocrinol ; 522: 111126, 2021 02 15.
Article in English | MEDLINE | ID: mdl-33321115

ABSTRACT

Diabetes is a genetically heterogeneous disease, for which we are aiming to identify causative genes. Here, we report a missense mutation (c.T1424C:p.L475P) in ZYG11A identified by exome sequencing as segregating with hyperglycemia in a Thai family with autosomal dominant diabetes. ZYG11A functions as a target recruitment subunit of an E3 ubiquitin ligase complex that plays an important role in the regulation of cell cycle. We demonstrate an increase in cells arrested at G2/mitotic phase among beta-cells deficient for ZYG11A or overexpressing L475P-ZYG11A, which is associated with a decreased growth rate. This is the first evidence linking a ZYG11A mutation to hyperglycemia, and suggesting ZYG11A as a cell cycle regulator required for beta-cell growth. Since most family members were either overweight or obese, but only mutation carriers developed hyperglycemia, our data also suggests the ZYG11A mutation as a genetic factor predisposing obese individuals to beta-cell failure in maintenance of glucose homeostasis.


Subject(s)
Cell Cycle Checkpoints/genetics , Cell Cycle Proteins/genetics , Diabetes Mellitus/genetics , Genes, Dominant , Insulin-Secreting Cells/pathology , Mutation/genetics , Adult , Aged , Aged, 80 and over , Amino Acid Sequence , Cell Cycle Proteins/chemistry , Cell Proliferation/genetics , Chromosome Segregation/genetics , Exome/genetics , Female , Humans , Male , Middle Aged , Models, Biological , Models, Molecular , Pedigree
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