Literature DB >> 22262174

Cdc6 is required for meiotic spindle assembly in Xenopus oocytes.

Yadushyla Narasimhachar1, Daniel R Webster, David L Gard, Martine Coué.   

Abstract

During the maturation of Xenopus oocytes, Cdc6 expression is necessary to establish replication competence to support early embryonic DNA replication. However, Cdc6 is expressed before the completion of MI, at a time when its function as a replication factor is not required, suggesting additional roles for Cdc6 in meiosis. Confocal immunofluorescence microscopy revealed that Cdc6 protein was distributed around the spindle precursor at the time of germinal vesicle breakdown (GVBD), and localized to the margin of the nascent spindle early in prometaphase. Cdc6 subsequently localized to spindle poles in late prometaphase, where it remained until metaphase arrest. Microinjection of antisense oligonucleotides specific for Cdc6 mRNA disrupted spindle assembly, resulting in defects including delayed spindle assembly, misoriented and unattached anaphase spindles, monasters, multiple spindles, microtubule aggregates associated with condensed chromosomes, or the absence of recognizable spindle-like structures, depending on the level of residual Cdc6 expression. Furthermore, Cdc6 co-localized with γ-tubulin in centrosomes during interphase in all somatic cells analyzed, and associated with spindle poles in mitotic COS cells. Our data suggest a role for Cdc6 in spindle formation in addition to its role as a DNA replication factor.

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Year:  2012        PMID: 22262174      PMCID: PMC3315094          DOI: 10.4161/cc.11.3.19033

Source DB:  PubMed          Journal:  Cell Cycle        ISSN: 1551-4005            Impact factor:   4.534


  36 in total

1.  Residual Cdc2 activity remaining at meiosis I exit is essential for meiotic M-M transition in Xenopus oocyte extracts.

Authors:  M Iwabuchi; K Ohsumi; T M Yamamoto; W Sawada; T Kishimoto
Journal:  EMBO J       Date:  2000-09-01       Impact factor: 11.598

2.  Cdc6 synthesis regulates replication competence in Xenopus oocytes.

Authors:  Elizabeth Whitmire; Bettina Khan; Martine Coué
Journal:  Nature       Date:  2002-10-17       Impact factor: 49.962

3.  Functional analysis of bacterial artificial chromosomes in mammalian cells: mouse Cdc6 is associated with the mitotic spindle apparatus.

Authors:  Sharon Illenye; Nicholas H Heintz
Journal:  Genomics       Date:  2004-01       Impact factor: 5.736

4.  Orc6 involved in DNA replication, chromosome segregation, and cytokinesis.

Authors:  Supriya G Prasanth; Kannanganattu V Prasanth; Bruce Stillman
Journal:  Science       Date:  2002-08-09       Impact factor: 47.728

5.  Competence to replicate in the unfertilized egg is conferred by Cdc6 during meiotic maturation.

Authors:  Jean-Marc Lemaître; Stéphane Bocquet; Marcel Méchali
Journal:  Nature       Date:  2002-10-17       Impact factor: 49.962

6.  Geminin deficiency causes a Chk1-dependent G2 arrest in Xenopus.

Authors:  Thomas J McGarry
Journal:  Mol Biol Cell       Date:  2002-10       Impact factor: 4.138

7.  XMAP215, XKCM1, NuMA, and cytoplasmic dynein are required for the assembly and organization of the transient microtubule array during the maturation of Xenopus oocytes.

Authors:  Bret E Becker; S Joshua Romney; David L Gard
Journal:  Dev Biol       Date:  2003-09-15       Impact factor: 3.582

8.  The regulation of competence to replicate in meiosis by Cdc6 is conserved during evolution.

Authors:  Jean-Marc Lemaître; Stéphane Bocquet; Marie-Emilie Terret; Mandana Namdar; Ounissa Aït-Ahmed; Stephen Kearsey; Marie-Hélène Verlhac; Marcel Méchali
Journal:  Mol Reprod Dev       Date:  2004-09       Impact factor: 2.609

9.  Human Orc2 localizes to centrosomes, centromeres and heterochromatin during chromosome inheritance.

Authors:  Supriya G Prasanth; Kannanganattu V Prasanth; Khalid Siddiqui; David L Spector; Bruce Stillman
Journal:  EMBO J       Date:  2004-06-24       Impact factor: 11.598

10.  CDK-1 inhibits meiotic spindle shortening and dynein-dependent spindle rotation in C. elegans.

Authors:  Marina L Ellefson; Francis J McNally
Journal:  J Cell Biol       Date:  2011-06-20       Impact factor: 10.539

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  4 in total

1.  The DNA replication protein Cdc6 inhibits the microtubule-organizing activity of the centrosome.

Authors:  Inyoung Lee; Gwang Su Kim; Jun Sung Bae; Jaeyoun Kim; Kunsoo Rhee; Deog Su Hwang
Journal:  J Biol Chem       Date:  2017-08-21       Impact factor: 5.157

2.  Systems-level quantification of division timing reveals a common genetic architecture controlling asynchrony and fate asymmetry.

Authors:  Vincy Wing Sze Ho; Ming-Kin Wong; Xiaomeng An; Daogang Guan; Jiaofang Shao; Hon Chun Kaoru Ng; Xiaoliang Ren; Kan He; Jinyue Liao; Yingjin Ang; Long Chen; Xiaotai Huang; Bin Yan; Yiji Xia; Leanne Lai Hang Chan; King Lau Chow; Hong Yan; Zhongying Zhao
Journal:  Mol Syst Biol       Date:  2015-06-10       Impact factor: 11.429

3.  Zebrafish cdc6 hypomorphic mutation causes Meier-Gorlin syndrome-like phenotype.

Authors:  Likun Yao; Jing Chen; Xiaotong Wu; Shunji Jia; Anming Meng
Journal:  Hum Mol Genet       Date:  2017-11-01       Impact factor: 6.150

4.  Mathematical Model Explaining the Role of CDC6 in the Diauxic Growth of CDK1 Activity during the M-Phase of the Cell Cycle.

Authors:  Mateusz Dębowski; Zuzanna Szymańska; Jacek Z Kubiak; Mirosław Lachowicz
Journal:  Cells       Date:  2019-11-28       Impact factor: 6.600

  4 in total

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