@article{SchweigelBatsiosMuellerTaubenbergeretal.2022, author = {Schweigel, Ulrike and Batsios, Petros and M{\"u}ller-Taubenberger, Annette and Gr{\"a}f, Ralph and Grafe, Marianne}, title = {Dictyostelium spastin is involved in nuclear envelope dynamics during semi-closed mitosis}, series = {Nucleus}, volume = {13}, journal = {Nucleus}, number = {1}, publisher = {Taylor \& Francis Group}, address = {Philadelphia}, issn = {1949-1034}, doi = {10.1080/19491034.2022.2047289}, pages = {144 -- 154}, year = {2022}, abstract = {Dictyostelium amoebae perform a semi-closed mitosis, in which the nuclear envelope is fenestrated at the insertion sites of the mitotic centrosomes and around the central spindle during karyokinesis. During late telophase the centrosome relocates to the cytoplasmic side of the nucleus, the central spindle disassembles and the nuclear fenestrae become closed. Our data indicate that Dictyostelium spastin (DdSpastin) is a microtubule-binding and severing type I membrane protein that plays a role in this process. Its mitotic localization is in agreement with a requirement for the removal of microtubules that would hinder closure of the fenestrae. Furthermore, DdSpastin interacts with the HeH/ LEM-family protein Src1 in BioID analyses as well as the inner nuclear membrane protein Sun1, and shows subcellular co-localizations with Src1, Sun1, the ESCRT component CHMP7 and the IST1-like protein filactin, suggesting that the principal pathway of mitotic nuclear envelope remodeling is conserved between animals and Dictyostelium amoebae.}, language = {en} } @article{GraefGrafeMeyeretal.2021, author = {Gr{\"a}f, Ralph and Grafe, Marianne and Meyer, Irene and Mitic, Kristina and Pitzen, Valentin}, title = {The dictyostelium centrosome}, series = {Cells : open access journal}, volume = {10}, journal = {Cells : open access journal}, number = {10}, publisher = {MDPI}, address = {Basel}, issn = {2073-4409}, doi = {10.3390/cells10102657}, pages = {26}, year = {2021}, abstract = {The centrosome of Dictyostelium amoebae contains no centrioles and consists of a cylindrical layered core structure surrounded by a corona harboring microtubule-nucleating gamma-tubulin complexes. It is the major centrosomal model beyond animals and yeasts. Proteomics, protein interaction studies by BioID and superresolution microscopy methods led to considerable progress in our understanding of the composition, structure and function of this centrosome type. We discuss all currently known components of the Dictyostelium centrosome in comparison to other centrosomes of animals and yeasts.}, language = {en} }