机构地区:[1]MOE Key Laboratory for Cellular Dynamics&Anhui Key Laboratory for Chemical Biology,CAS Center for Excellence in Molecular Cell Science,Hefei National Science Center for Physical Sciences at Microscale&University of Science and Technology of China,Hefei 230027,China [2]Department of Physiology,Morehouse School of Medicine,Atlanta,GA 30310,USA [3]School of Basic Medical Sciences,Beijing University of Chinese Medicine,Beijing 100029,China [4]Department of Biology,Duke University Durham,NC 27708,USA [5]Institute of ProteoGenomics,Beijing 100029,China [6]Harvard Medical School,Boston,MA 02115,USA
出 处:《Journal of Molecular Cell Biology》2020年第8期654-665,共12页分子细胞生物学报(英文版)
基 金:This work was supported in part by the National NaturalScience Foundation of China(31430054,31320103904,31621002,31671405,31601097,91854203,91753000,and91853115);'Strategic Priority Research Program'of the ChineseAcademy of Sciences(XDB19000000);the National Key Researchand Development Program of China(2017YFA0503600 and2016YFA-0100500);MOE Innovative Team project(IRT_17R102);and the US National Institutes of Health(CA164133,DK56292,and DK115812).
摘 要:Error-free cell division depends on the accurate assembly of the spindle midzone from dynamic spindle microtubules to ensure chromatid segregation during metaphase-anaphase transition.However,the mechanism underlying the key transition from the mitotic spindle to central spindle before anaphase onset remains elusive.Given the prevalence of chromosome instability phenotype in gastric tumorigenesis,we developed a strategy to model context-dependent cell division using a combination of light sheet microscope and 3D gastric organoids.Light sheet microscopic image analyses of 3D organoids showed that CENP-E inhibited cells undergoing aberrant metaphase-anaphase transition and exhibiting chromosome segregation errors during mitosis.Highresolution real-time imaging analyses of 2D cell culture revealed that CENP-E inhibited cells undergoing central spindle splitting and chromosome instability phenotype.Using biotinylated syntelin as an affinity matrix,we found that CENP-E forms a complex with PRC1 in mitotic cells.Chemical inhibition of CENP-E in metaphase by syntelin prevented accurate central spindle assembly by perturbing temporal assembly of PRC1 to the midzone.Thus,CENP-E-mediated PRC1 assembly to the central spindle constitutes a temporal switch to organize dynamic kinetochore microtubules into stable midzone arrays.These findings reveal a previously uncharacterized role of CENP-E in temporal control of central spindle assembly.Since CENP-E is absent from yeast,we reasoned that metazoans evolved an elaborate central spindle organization machinery to ensure accurate sister chromatid segregation during anaphase and cytokinesis.
关 键 词:organoids.cell division central spindle CENP-E syntelin PRC1
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