Structural and calorimetric studies demonstrate that the hepatocyte nuclear factor 1β (HNF1β) transcription factor is imported into the nucleus via a monopartite NLS sequence

التفاصيل البيبلوغرافية
العنوان: Structural and calorimetric studies demonstrate that the hepatocyte nuclear factor 1β (HNF1β) transcription factor is imported into the nucleus via a monopartite NLS sequence
المؤلفون: Mareike M. Wiedmann, Murray Stewart, Shintaro Aibara, James D. Brenton, David R. Spring
المساهمون: Spring, David [0000-0001-7355-2824], Brenton, James [0000-0002-5738-6683], Apollo - University of Cambridge Repository
المصدر: Journal of Structural Biology
بيانات النشر: Elsevier BV, 2016.
سنة النشر: 2016
مصطلحات موضوعية: Models, Molecular, Protein Conformation, alpha-Helical, 0301 basic medicine, mImportin-α, mouse Importin-α, Nuclear Localization Signals, Nuclear import pathway, Xenopus Proteins, Crystallography, X-Ray, environment and public health, GST, glutathione S-transferase, HNF1βDBD, HNF1β DNA binding domain, Mice, Xenopus laevis, 0302 clinical medicine, Sequence Analysis, Protein, Structural Biology, Nuclear protein, CCC, ovarian clear cell carcinoma, IBB, Importin-β-binding domain, Hepatocyte nuclear factor-1β (HNF1β), Nuclear localisation signal sequence (NLS), 3. Good health, Cell biology, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Isothermal titration calorimetry, Protein Binding, alpha Karyopherins, Active Transport, Cell Nucleus, Importin, Biology, Article, HNF1β, hepatocyte nuclear factor 1β, 03 medical and health sciences, Importin-α, Cell Line, Tumor, medicine, Animals, Humans, Transcription factor, Hepatocyte Nuclear Factor 1-beta, X-ray crystallography, Cell Nucleus, Site-directed mutagenesis, Binding Sites, xImportin-α, Xenopus Importin-α, DNA-binding domain, Molecular biology, Cell nucleus, HEK293 Cells, 030104 developmental biology, NLS, nuclear localization signal, Hepatocyte Nuclear Factor 1-Beta, Nuclear transport, Nuclear localization sequence
الوصف: The transcription factor hepatocyte nuclear factor 1β (HNF1β) is ubiquitously overexpressed in ovarian clear cell carcinoma (CCC) and is a potential therapeutic target. To explore potential approaches that block HNF1β transcription we have identified and characterised extensively the nuclear localisation signal (NLS) for HNF1β and its interactions with the nuclear protein import receptor, Importin-α. Pull-down assays demonstrated that the DNA binding domain of HNF1β interacted with a spectrum of Importin-α isoforms and deletion constructs tagged with eGFP confirmed that the HNF1β 229KKMRRNR235 sequence was essential for nuclear localisation. We further characterised the interaction between the NLS and Importin-α using complementary biophysical techniques and have determined the 2.4Å resolution crystal structure of the HNF1β NLS peptide bound to Importin-α. The functional, biochemical, and structural characterisation of the nuclear localisation signal present on HNF1β and its interaction with the nuclear import protein Importin-α provide the basis for the development of compounds targeting transcription factor HNF1β via its nuclear import pathway.
وصف الملف: application/pdf
تدمد: 1047-8477
DOI: 10.1016/j.jsb.2016.06.018
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07cdc136a8a8b67b570e14b2d6984d3fTest
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....07cdc136a8a8b67b570e14b2d6984d3f
قاعدة البيانات: OpenAIRE
الوصف
تدمد:10478477
DOI:10.1016/j.jsb.2016.06.018