Inviting an author to review:
Find an author and click ‘Invite to review selected article’ near their name.
Search for authorsSearch for similar articles
35
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      A Requirement of Nudel and Dynein for Assembly of the Lamin B Spindle Matrix

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Guanosine triphosphatase Ran (RanGTP) can stimulate assembly of the type V intermediate filament protein, lamin B, into a membranous lamin B spindle matrix, which is required for proper microtubule organization during spindle assembly. Microtubules in turn enhance assembly of the matrix. We report here that the isolated matrix contains known spindle assembly factors such as dynein and Nudel. Using spindle assembly assays in Xenopus egg extracts, we show that Nudel regulates microtubule organization during spindle assembly independent of its function at kinetochores. Importantly, Nudel directly interacts with lamin B to facilitate the accumulation and assembly of lamin B-containing matrix on microtubules in a dynein-dependent manner. Perturbing either Nudel or dynein inhibited assembly of lamin B matrix. However, depleting lamin B still allowed formation of matrices containing dynein and Nudel. Therefore, dynein and Nudel regulate assembly of the lamin B matrix. Interestingly, we found that whereas depleting lamin B resulted in disorganized spindle and spindle poles, disrupting the function of Nudel or dynein caused a complete lack of spindle pole focusing. We suggest that Nudel regulates microtubule organization in part by facilitating assembly of the lamin B spindle matrix in a dynein-dependent manner.

          Related collections

          Most cited references24

          • Record: found
          • Abstract: found
          • Article: not found

          Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen.

          Small molecules that perturb specific protein functions are valuable tools for dissecting complex processes in mammalian cells. A combination of two phenotype-based screens, one based on a specific posttranslational modification, the other visualizing microtubules and chromatin, was used to identify compounds that affect mitosis. One compound, here named monastrol, arrested mammalian cells in mitosis with monopolar spindles. In vitro, monastrol specifically inhibited the motility of the mitotic kinesin Eg5, a motor protein required for spindle bipolarity. All previously known small molecules that specifically affect the mitotic machinery target tubulin. Monastrol will therefore be a particularly useful tool for studying mitotic mechanisms.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            The nuclear lamina comes of age.

            Many nuclear proteins form lamin-dependent complexes, including LEM-domain proteins, nesprins and SUN-domain proteins. These complexes have roles in chromatin organization, gene regulation and signal transduction. Some link the nucleoskeleton to cytoskeletal structures, ensuring that the nucleus and centrosome assume appropriate intracellular positions. These complexes provide new insights into cell architecture, as well as a foundation for the understanding of the molecular mechanisms that underlie the human laminopathies - clinical disorders that range from Emery-Dreifuss muscular dystrophy to the accelerated ageing seen in Hutchinson-Gilford progeria syndrome.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              A complex of NuMA and cytoplasmic dynein is essential for mitotic spindle assembly.

              NuMA is a nuclear protein during interphase but redistributes to the spindle poles early in mitosis. To investigate its role during spindle formation, we tested spindle assembly in frog egg extracts from which NuMA was immunodepleted. Immunodepletion revealed that NuMA forms a complex with cytoplasmic dynein and dynactin. The depleted extracts failed to assemble normal mitotic spindles, producing, instead, chromatin-associated irregular arrays of microtubules lacking characteristic spindle poles. A subdomain of the NuMA tail was shown to induce microtubule aster formation by mediating microtubule bundling. Our findings suggest that NuMA forms bifunctional complexes with cytoplasmic dynein and dynactin that can tether microtubules at the spindle poles and that are essential for mitotic spindle pole assembly and stabilization.
                Bookmark

                Author and article information

                Journal
                100890575
                21417
                Nat Cell Biol
                Nature cell biology
                1465-7392
                1476-4679
                17 March 2009
                8 February 2009
                March 2009
                1 September 2009
                : 11
                : 3
                : 247-256
                Affiliations
                [1 ]Laboratory of Molecular Cell Biology and Center of Cell Signaling, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China
                [2 ]Department of Embryology, Carnegie Institution for Science and Howard Hughes Medical Institute, Baltimore, Maryland, United States of America
                [3 ]Department of Cell Biology, The Scripps Research Institute, La Jolla, California, United States of America
                [4 ]Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
                Author notes
                [* ]Correspondence: Yixian Zheng ( zheng@ 123456ciwemb.edu ) and Xueliang Zhu ( xlzhu@ 123456sibs.ac.cn )
                Article
                nihpa100611
                10.1038/ncb1832
                2699591
                19198602
                678179c8-05b5-4c40-bda6-7706bfda45f6
                History
                Funding
                Funded by: National Institute of General Medical Sciences : NIGMS
                Funded by: Howard Hughes Medical Institute
                Award ID: R01 GM056312-10A2 ||GM
                Funded by: National Institute of General Medical Sciences : NIGMS
                Funded by: Howard Hughes Medical Institute
                Award ID: ||HHMI_
                Categories
                Article

                Cell biology
                cell fate determinants,dynein,lamin b spindle matrix,mitosis,nudel,membrane partitioning
                Cell biology
                cell fate determinants, dynein, lamin b spindle matrix, mitosis, nudel, membrane partitioning

                Comments

                Comment on this article