Literature DB >> 17687118

Spatio-temporal expression patterns of aurora kinases a, B, and C and cytoplasmic polyadenylation-element-binding protein in bovine oocytes during meiotic maturation.

Svetlana Uzbekova1, Yannick Arlot-Bonnemains, Joëlle Dupont, Rozenn Dalbiès-Tran, Pascal Papillier, Sophie Pennetier, Aurore Thélie, Christine Perreau, Pascal Mermillod, Claude Prigent, Rustem Uzbekov.   

Abstract

Maturation of immature bovine oocytes requires cytoplasmic polyadenylation and synthesis of a number of proteins involved in meiotic progression and metaphase-II arrest. Aurora serine-threonine kinases--localized in centrosomes, chromosomes, and midbody--regulate chromosome segregation and cytokinesis in somatic cells. In frog and mouse oocytes, Aurora A regulates polyadenylation-dependent translation of several mRNAs such as MOS and CCNB1, presumably by phosphorylating CPEB, and Aurora B phosphorylates histone H3 during meiosis. We analyzed the expression of three Aurora kinase genes--AURKA, AURKB, and AURKC--in bovine oocytes during meiosis by reverse transcription followed by quantitative real-time PCR and immunodetection. Aurora A was the most abundant form in oocytes, both at mRNA and protein levels. AURKA protein progressively accumulated in the oocyte cytoplasm during antral follicle growth and in vitro maturation. AURKB associated with metaphase chromosomes. AURKB, AURKC, and Thr-phosphorylated AURKA were detected at a contractile ring/midbody during the first polar body extrusion. CPEB, localized in oocyte cytoplasm, was hyperphosphorylated during prophase/metaphase-I transition. Most CPEB degraded in metaphase-II oocytes and remnants remained localized in a contractile ring. Roscovitine, U0126, and metformin inhibited meiotic divisions; they all induced a decrease of CCNB1 and phospho-MAPK3/1 levels and prevented CPEB degradation. However, only metformin depleted AURKA. The Aurora kinase inhibitor VX680 at 100 nmol/L did not inhibit meiosis but led to multinuclear oocytes due to the failure of the polar body extrusion. Thus, in bovine oocyte meiosis, massive destruction of CPEB accompanies metaphase-I/II transition, and Aurora kinases participate in regulating segregation of the chromosomes, maintenance of metaphase-II, and formation of the first polar body.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17687118     DOI: 10.1095/biolreprod.107.061036

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  25 in total

1.  Polar body emission requires a RhoA contractile ring and Cdc42-mediated membrane protrusion.

Authors:  Xuan Zhang; Chunqi Ma; Ann L Miller; Hadia Arabi Katbi; William M Bement; X Johné Liu
Journal:  Dev Cell       Date:  2008-09       Impact factor: 12.270

2.  The impact of vitrification on murine germinal vesicle oocyte In vitro maturation and aurora kinase A protein expression.

Authors:  Joseph O Doyle; Ho Joon Lee; Kaisa Selesniemi; Aaron K Styer; Bo R Rueda
Journal:  J Assist Reprod Genet       Date:  2014-10-16       Impact factor: 3.412

3.  Urochordate ascidians possess a single isoform of Aurora kinase that localizes to the midbody via TPX2 in eggs and cleavage stage embryos.

Authors:  Celine Hebras; Alex McDougall
Journal:  PLoS One       Date:  2012-09-20       Impact factor: 3.240

4.  MAPK signaling couples SCF-mediated degradation of translational regulators to oocyte meiotic progression.

Authors:  Edyta Kisielnicka; Ryuji Minasaki; Christian R Eckmann
Journal:  Proc Natl Acad Sci U S A       Date:  2018-03-01       Impact factor: 11.205

5.  Oocytes isolated from dairy cows with reduced ovarian reserve have a high frequency of aneuploidy and alterations in the localization of progesterone receptor membrane component 1 and aurora kinase B.

Authors:  Alberto Maria Luciano; Federica Franciosi; Valentina Lodde; Irene Tessaro; Davide Corbani; Silvia Clotilde Modina; John J Peluso
Journal:  Biol Reprod       Date:  2013-03-07       Impact factor: 4.285

6.  Aurora kinase A controls meiosis I progression in mouse oocytes.

Authors:  Adela Saskova; Petr Solc; Vladimir Baran; Michal Kubelka; Richard M Schultz; Jan Motlik
Journal:  Cell Cycle       Date:  2008-05-29       Impact factor: 4.534

7.  Aurora-C kinase deficiency causes cytokinesis failure in meiosis I and production of large polyploid oocytes in mice.

Authors:  Kuo-Tai Yang; Shu-Kuei Li; Chih-Chieh Chang; Chieh-Ju C Tang; Yi-Nan Lin; Sheng-Chung Lee; Tang K Tang
Journal:  Mol Biol Cell       Date:  2010-05-19       Impact factor: 4.138

8.  Proteasomal activity is required to initiate and to sustain translational activation of messenger RNA encoding the stem-loop-binding protein during meiotic maturation in mice.

Authors:  Qin Yang; Patrick Allard; Michael Huang; Wenling Zhang; Hugh J Clarke
Journal:  Biol Reprod       Date:  2009-09-16       Impact factor: 4.285

9.  Rhesus macaque embryos derived from MI oocytes maturing after retrieval display high rates of chromosomal anomalies.

Authors:  Cathérine Dupont; Barry D Bavister; D Randall Armant; Carol A Brenner
Journal:  Hum Reprod       Date:  2008-12-23       Impact factor: 6.918

10.  Perturbing microtubule integrity blocks AMP-activated protein kinase-induced meiotic resumption in cultured mouse oocytes.

Authors:  Ru Ya; Stephen M Downs
Journal:  Zygote       Date:  2012-11-16       Impact factor: 1.442

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.