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HNF1A-MODY Mutations in Nuclear Localization Signal Impair HNF1A-Import Receptor KPNA6 Interactions.
Fareed, Fareed M A; Korulu, Sirin; Özbil, Mehmet; Çapan, Özlem Yalçin.
Afiliación
  • Fareed FMA; Department of Molecular Biology and Genetics, Istanbul Arel University, 34537, Istanbul, Turkey.
  • Korulu S; Department of Chemistry, Yildiz Technical University, 34220, Istanbul, Turkey.
  • Özbil M; Institute of Natural and Health Sciences, Tallinn University, 10120, Tallinn, Estonia.
  • Çapan ÖY; Biotechnology Institute, Gebze Technical University, 41400, Kocaeli, Turkey.
Protein J ; 40(4): 512-521, 2021 08.
Article en En | MEDLINE | ID: mdl-33459938
Mutations in hepatocyte nuclear factor (HNF)1A gene cause the most common form of Maturity-onset diabetes of the young (MODY), a monogenic subtype of diabetes mellitus. Functional characterization of mutant proteins reveals that mutations may disrupt DNA binding capacity, transactivation ability and nuclear localization of HNF1A depending on the position of the mutation. Previously identified Arg271Trp and Ser345Tyr mutations in HNF1A were found to be defective in nuclear localization. Arg271 residue resides in a region similar to classical nuclear localization signal (NLS) motif, while Ser345 does not. Importin α family members recognize NLS motifs on cargo proteins and subsequently translocate them into nucleus. Here, we first investigated the nuclear localization mechanism of wild type HNF1A protein. For this purpose, we analyzed the interaction of HNF1A with three mouse homolog importin α proteins (KPNA2, KPNA4 and KPNA6) by co-immunoprecipitation assay and molecular docking simulation. Hereby, KPNA6 was identified as the main import receptor, which is responsible for the transport of HNF1A into the nucleus. Immunolocalization studies in mouse pancreatic cells (Min6) also confirmed the co-localization of HNF1A and KPNA6 in the cytoplasm. Secondly, the interaction between KPNA6 and mutant HNF1A proteins (Arg271Trp and Ser345Tyr) was assessed. Co-immunoprecipitation studies revealed a reduced interaction compared to wild type HNF1A. Our study demonstrated for the first time that HNF1A transcription factor is recognized and transported by importin/karyopherin import family, and mutations in NLS motifs may disrupt the interaction leading to nuclear localization abnormalities and MODY phenotype.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Señales de Localización Nuclear / Mutación Missense / Alfa Carioferinas / Diabetes Mellitus Tipo 2 / Factor Nuclear 1-alfa del Hepatocito Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Protein J Asunto de la revista: BIOQUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Señales de Localización Nuclear / Mutación Missense / Alfa Carioferinas / Diabetes Mellitus Tipo 2 / Factor Nuclear 1-alfa del Hepatocito Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Protein J Asunto de la revista: BIOQUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Países Bajos