Literature DB >> 15389869

Chromator, a novel and essential chromodomain protein interacts directly with the putative spindle matrix protein skeletor.

Uttama Rath1, Dong Wang, Yun Ding, Ying-Zhi Xu, Hongying Qi, Melissa J Blacketer, Jack Girton, Jørgen Johansen, Kristen M Johansen.   

Abstract

We have used a yeast two-hybrid interaction assay to identify Chromator, a novel chromodomain containing protein that interacts directly with the putative spindle matrix protein Skeletor. Immunocytochemistry demonstrated that Chromator and Skeletor show extensive co-localization throughout the cell cycle. During interphase Chromator is localized on chromosomes to interband chromatin regions in a pattern that overlaps that of Skeletor. However, during mitosis both Chromator and Skeletor detach from the chromosomes and align together in a spindle-like structure. Deletion construct analysis in S2 cells showed that the COOH-terminal half of Chromator without the chromodomain was sufficient for both nuclear as well as spindle localization. Analysis of P-element mutations in the Chromator locus shows that Chromator is an essential protein. Furthermore, RNAi depletion of Chromator in S2 cells leads to abnormal microtubule spindle morphology and to chromosome segregation defects. These findings suggest that Chromator is a nuclear protein that plays a role in proper spindle dynamics during mitosis. (c) 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15389869     DOI: 10.1002/jcb.20243

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  40 in total

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8.  The COOH-terminal domain of the JIL-1 histone H3S10 kinase interacts with histone H3 and is required for correct targeting to chromatin.

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9.  Lamin B counteracts the kinesin Eg5 to restrain spindle pole separation during spindle assembly.

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10.  Megator, an essential coiled-coil protein that localizes to the putative spindle matrix during mitosis in Drosophila.

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