CENP-C/H/I/K/M/T/W/N/L and hMis12 but not CENP-S/X participate in complex formation in the nucleoplasm of living human interphase cells outside centromeres

• المؤلفون الرئيسيون: Hoischen C., Yavas S., Wohland T., Diekmann S.
• مؤلفون آخرون: BIOLOGICAL SCIENCES
• التنسيق: مقال
• منشور في: Public Library of Science 2020
• الموضوعات: binding protein; centromere protein C; centromere protein H; centromere protein I; centromere protein K; centromere protein L; centromere protein M; centromere protein N; centromere protein O; centromere protein P; centromere protein Q; centromere protein R; centromere protein S; centromere protein T; centromere protein U; centromere protein W; centromere protein X; Dsn1 protein; heterodimer; Mis12 protein; Nnf1 protein; Nsl1 protein; nuclear protein; unclassified drug; APITD1 protein, human; apoptosis regulatory protein; cell cycle protein; CENPH protein, human; CENPI protein, human; CENPK protein, human; CENPL protein, human; CENPN protein, human; CENPW protein, human; DNA binding protein; microtubule associated protein; MIS12 protein, human; nonhistone protein; proliferation associated nuclear element protein 1, human; STRA13 protein, human; tumor protein; tumor suppressor protein; amino terminal sequence; apparent dissociation constant; Article; binding site; carboxy terminal sequence; cell component; cell nucleus; cellular distribution; centromere; complex formation; controlled study; DNA binding; embryo; fluorescence correlation spectroscopy; human; human cell; kinetochore; nucleoplasm; protein aggregation; protein expression; protein localization; protein protein interaction; genetics; interphase; metabolism; neoplasm; pathology; tumor cell line; Apoptosis Regulatory Proteins; Cell Cycle Proteins; Cell Line, Tumor; Centromere; Chromosomal Proteins, Non-Histone; DNA-Binding Proteins; Humans; Interphase; Microtubule-Associated Proteins; Neoplasm Proteins; Neoplasms; Nuclear Proteins; Tumor Suppressor Proteins
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/165911

10.1371/journal.pone.0192572