Transient expression was reported in mouse islets during gestation， whereas a genome-wide linkage and admixture mapping study highlighted as a candidate gene for diabetes mellitus (DM). We sought the significance of PAX8 expression in mouse and human islet biology. was induced in gestating mouse islets and in human islets treated with recombinant prolactin. Global gene expression profiling of human and mouse islets overexpressing the corresponding species-specific PAX8 revealed the modulation of distinct genetic pathways that converge on cell survival. Accordingly， apoptosis was reduced in PAX8-overexpressing islets. These findings support that could be a candidate gene for the study of gestational DM (... More
Transient expression was reported in mouse islets during gestation， whereas a genome-wide linkage and admixture mapping study highlighted as a candidate gene for diabetes mellitus (DM). We sought the significance of PAX8 expression in mouse and human islet biology. was induced in gestating mouse islets and in human islets treated with recombinant prolactin. Global gene expression profiling of human and mouse islets overexpressing the corresponding species-specific PAX8 revealed the modulation of distinct genetic pathways that converge on cell survival. Accordingly， apoptosis was reduced in PAX8-overexpressing islets. These findings support that could be a candidate gene for the study of gestational DM (GDM). was genotyped in patients with GDM and gestational thyroid dysfunction (GTD)， a pathology commonly found in patients with mutations on A novel missense mutation (p.T356M， c.1067C>T) was identified in a female diagnosed with GDM and GTD as well as in her father with type 2 DM but was absent in control patients. The p.T356M variant did not alter protein stability or cellular localization， whereas its transactivation activity was hindered. In parallel， a retrospective clinical analysis uncovered that a pregnant female harboring a second mutation (p.P25R， c.74C>G) previously reported to cause congenital hypothyroidism also developed GDM. These data indicate that increased expression of PAX8 affects islet viability and that could be considered as a candidate gene for the study of GDM.
