Literature DB >> 22735043

CDC-48/p97 is required for proper meiotic chromosome segregation via controlling AIR-2/Aurora B kinase localization in Caenorhabditis elegans.

Yohei Sasagawa1, Atsushi Higashitani, Takeshi Urano, Teru Ogura, Kunitoshi Yamanaka.   

Abstract

CDC-48/p97 is a AAA (ATPases associated with diverse cellular activities) chaperone involved in protein conformational changes such as the disassembly of protein complexes. We previously reported that Caenorhabditis elegans CDC-48.1 and CDC-48.2 (CDC-48s) are essential for the progression of meiosis I metaphase. Here, we report that CDC-48s are required for proper chromosome segregation during meiosis in C. elegans. In wild-type worms, at the diakinesis phase, phosphorylation of histone H3, one of the known substrates of aurora B kinase (AIR-2), on meiosis I chromatids correlated with AIR-2 localization at the cohesion sites of homologous chromatids. Conversely, depletion of CDC-48s resulted in a significant expansion of signals for AIR-2 and phosphorylated histone H3 over the entire length of meiotic chromosomes, leading to defective chromosome segregation, while the total amount of AIR-2 in lysates was not changed by the depletion of CDC-48s. The defective segregation of meiotic chromosomes caused by the depletion of CDC-48s was suppressed by the simultaneous depletion of AIR-2 and is similar to that observed following the depletion of protein phosphatase 1 (PP1) phosphatases. However, the amount and localization of PP1 were not changed by the depletion of CDC-48s. These results suggest that CDC-48s control the restricted localization of AIR-2 to the cohesion sites of homologous chromatids in meiosis I.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22735043     DOI: 10.1016/j.jsb.2012.06.009

Source DB:  PubMed          Journal:  J Struct Biol        ISSN: 1047-8477            Impact factor:   2.867


  6 in total

1.  Inadequate fine-tuning of protein synthesis and failure of amino acid homeostasis following inhibition of the ATPase VCP/p97.

Authors:  K Parzych; T M Chinn; Z Chen; S Loaiza; F Porsch; G N Valbuena; M F Kleijnen; A Karadimitris; E Gentleman; H C Keun; H W Auner
Journal:  Cell Death Dis       Date:  2015-12-31       Impact factor: 8.469

Review 2.  A Mighty "Protein Extractor" of the Cell: Structure and Function of the p97/CDC48 ATPase.

Authors:  Yihong Ye; Wai Kwan Tang; Ting Zhang; Di Xia
Journal:  Front Mol Biosci       Date:  2017-06-13

3.  The coordinated action of VCP/p97 and GCN2 regulates cancer cell metabolism and proteostasis during nutrient limitation.

Authors:  Katarzyna Parzych; Paula Saavedra-García; Gabriel N Valbuena; Hibah A Al-Sadah; Mark E Robinson; Lucy Penfold; Desislava M Kuzeva; Angie Ruiz-Tellez; Sandra Loaiza; Viktoria Holzmann; Valentina Caputo; David C Johnson; Martin F Kaiser; Anastasios Karadimitris; Eric W-F Lam; Eric Chevet; Niklas Feldhahn; Hector C Keun; Holger W Auner
Journal:  Oncogene       Date:  2019-01-09       Impact factor: 9.867

4.  The UBXN-2/p37/p47 adaptors of CDC-48/p97 regulate mitosis by limiting the centrosomal recruitment of Aurora A.

Authors:  Elsa Kress; Françoise Schwager; René Holtackers; Jonas Seiler; François Prodon; Esther Zanin; Annika Eiteneuer; Mika Toya; Asako Sugimoto; Hemmo Meyer; Patrick Meraldi; Monica Gotta
Journal:  J Cell Biol       Date:  2013-05-06       Impact factor: 10.539

5.  Role of p97/VCP (Cdc48) in genome stability.

Authors:  Bruno Vaz; Swagata Halder; Kristijan Ramadan
Journal:  Front Genet       Date:  2013-04-30       Impact factor: 4.599

Review 6.  Ring of Change: CDC48/p97 Drives Protein Dynamics at Chromatin.

Authors:  André Franz; Leena Ackermann; Thorsten Hoppe
Journal:  Front Genet       Date:  2016-05-03       Impact factor: 4.599

  6 in total

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