Literature DB >> 21482765

Identification and characterization of an oocyte factor required for development of porcine nuclear transfer embryos.

Kei Miyamoto1, Kouhei Nagai, Naoya Kitamura, Tomoaki Nishikawa, Haruka Ikegami, Nguyen T Binh, Satoshi Tsukamoto, Mai Matsumoto, Tomoyuki Tsukiyama, Naojiro Minami, Masayasu Yamada, Hiroyoshi Ariga, Masashi Miyake, Tatsuo Kawarasaki, Kazuya Matsumoto, Hiroshi Imai.   

Abstract

Nuclear reprogramming of differentiated cells can be induced by oocyte factors. Despite numerous attempts, these factors and mechanisms responsible for successful reprogramming remain elusive. Here, we identify one such factor, necessary for the development of nuclear transfer embryos, using porcine oocyte extracts in which some reprogramming events are recapitulated. After incubating somatic nuclei in oocyte extracts from the metaphase II stage, the oocyte proteins that were specifically and abundantly incorporated into the nuclei were identified by mass spectrometry. Among 25 identified proteins, we especially focused on a multifunctional protein, DJ-1. DJ-1 is present at a high concentration in oocytes from the germinal vesicle stage until embryos at the four-cell stage. Inhibition of DJ-1 function compromises the development of nuclear transfer embryos but not that of fertilized embryos. Microarray analysis of nuclear transfer embryos in which DJ-1 function is inhibited shows perturbed expression of P53 pathway components. In addition, embryonic arrest of nuclear transfer embryos injected with anti-DJ-1 antibody is rescued by P53 inhibition. We conclude that DJ-1 is an oocyte factor that is required for development of nuclear transfer embryos. This study presents a means for identifying natural reprogramming factors in mammalian oocytes and a unique insight into the mechanisms underlying reprogramming by nuclear transfer.

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Year:  2011        PMID: 21482765      PMCID: PMC3084120          DOI: 10.1073/pnas.1013634108

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  64 in total

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Journal:  J Biol Chem       Date:  2007-11-26       Impact factor: 5.157

2.  Hsp27 modulates p53 signaling and suppresses cellular senescence.

Authors:  Cornelia O'Callaghan-Sunol; Vladimir L Gabai; Michael Y Sherman
Journal:  Cancer Res       Date:  2007-12-15       Impact factor: 12.701

3.  Sumoylation is critical for DJ-1 to repress p53 transcriptional activity.

Authors:  Jun Fan; Haigang Ren; Erkang Fei; Nali Jia; Zheng Ying; Peng Jiang; Mian Wu; Guanghui Wang
Journal:  FEBS Lett       Date:  2008-03-11       Impact factor: 4.124

Review 4.  Stem cells, the molecular circuitry of pluripotency and nuclear reprogramming.

Authors:  Rudolf Jaenisch; Richard Young
Journal:  Cell       Date:  2008-02-22       Impact factor: 41.582

5.  Nuclear transfer and iPS may work best together.

Authors:  John Gurdon; Alison Murdoch
Journal:  Cell Stem Cell       Date:  2008-02-07       Impact factor: 24.633

6.  Defining molecular cornerstones during fibroblast to iPS cell reprogramming in mouse.

Authors:  Matthias Stadtfeld; Nimet Maherali; David T Breault; Konrad Hochedlinger
Journal:  Cell Stem Cell       Date:  2008-02-14       Impact factor: 24.633

7.  DJ-1, a novel oncogene which transforms mouse NIH3T3 cells in cooperation with ras.

Authors:  D Nagakubo; T Taira; H Kitaura; M Ikeda; K Tamai; S M Iguchi-Ariga; H Ariga
Journal:  Biochem Biophys Res Commun       Date:  1997-02-13       Impact factor: 3.575

8.  RNA binding activity of the recessive parkinsonism protein DJ-1 supports involvement in multiple cellular pathways.

Authors:  Marcel P van der Brug; Jeff Blackinton; Jayanth Chandran; Ling-Yang Hao; Ashish Lal; Krystyna Mazan-Mamczarz; Jennifer Martindale; Chengsong Xie; Rili Ahmad; Kelly J Thomas; Alexandra Beilina; J Raphael Gibbs; Jinhui Ding; Amanda J Myers; Ming Zhan; Huaibin Cai; Nancy M Bonini; Myriam Gorospe; Mark R Cookson
Journal:  Proc Natl Acad Sci U S A       Date:  2008-07-14       Impact factor: 11.205

9.  14-3-3 zeta down-regulates p53 in mammary epithelial cells and confers luminal filling.

Authors:  Christopher G Danes; Shannon L Wyszomierski; Jing Lu; Christopher L Neal; Wentao Yang; Dihua Yu
Journal:  Cancer Res       Date:  2008-03-15       Impact factor: 12.701

10.  Sequential expression of pluripotency markers during direct reprogramming of mouse somatic cells.

Authors:  Tobias Brambrink; Ruth Foreman; G Grant Welstead; Christopher J Lengner; Marius Wernig; Heikyung Suh; Rudolf Jaenisch
Journal:  Cell Stem Cell       Date:  2008-02-07       Impact factor: 24.633

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  20 in total

1.  Early aberrations in chromatin dynamics in embryos produced under in vitro conditions.

Authors:  Rahul S Deshmukh; Olga Østrup; Frantisek Strejcek; Morten Vejlsted; Andrea Lucas-Hahn; Bjorn Petersen; Juan Li; Henrik Callesen; Heiner Niemann; Poul Hyttel
Journal:  Cell Reprogram       Date:  2012-04-02       Impact factor: 1.987

2.  Proteomic analysis of early reprogramming events in murine somatic cells incubated with Xenopus laevis oocyte extracts demonstrates network associations with induced pluripotency markers.

Authors:  Alex J Rathbone; Susan Liddell; Keith H S Campbell
Journal:  Cell Reprogram       Date:  2013-06-15       Impact factor: 1.987

3.  Combined positive effect of oocyte extracts and brilliant cresyl blue stained recipient cytoplasts on epigenetic reprogramming and gene expression in buffalo nuclear transfer embryos.

Authors:  E M Sadeesh; Shah Fozia; Kataria Meena
Journal:  Cytotechnology       Date:  2017-01-09       Impact factor: 2.058

4.  Expression profile of developmentally important genes between hand-made cloned buffalo embryos produced from reprogramming of donor cell with oocytes extract and selection of recipient cytoplast through brilliant cresyl blue staining and in vitro fertilized embryos.

Authors:  Sadeesh Em; Meena Kataria; Balhara S; Ps Yadav
Journal:  J Assist Reprod Genet       Date:  2014-08-21       Impact factor: 3.412

5.  RE1-silencing Transcription Factor (REST) Is Required for Nuclear Reprogramming by Inhibiting Transforming Growth Factor β Signaling Pathway.

Authors:  Qing-Ran Kong; Bing-Teng Xie; Heng Zhang; Jing-Yu Li; Tian-Qing Huang; Ren-Yue Wei; Zhong-Hua Liu
Journal:  J Biol Chem       Date:  2016-11-07       Impact factor: 5.157

6.  Identification and characterization of an oocyte factor required for porcine nuclear reprogramming.

Authors:  Qingran Kong; Bingteng Xie; Jingyu Li; Yanjun Huan; Tianqing Huang; Renyue Wei; Jiawei Lv; Shichao Liu; Zhonghua Liu
Journal:  J Biol Chem       Date:  2014-01-28       Impact factor: 5.157

7.  Cell-free extract from porcine induced pluripotent stem cells can affect porcine somatic cell nuclear reprogramming.

Authors:  Jin-Gu No; Mi-Kyung Choi; Dae-Jin Kwon; Jae Gyu Yoo; Byoung-Chul Yang; Jin-Ki Park; Dong-Hoon Kim
Journal:  J Reprod Dev       Date:  2015-01-24       Impact factor: 2.214

8.  Discovery of porcine maternal factors related to nuclear reprogramming and early embryo development by proteomic analysis.

Authors:  Qi Zhao; Zheng Guo; Shanhua Piao; Chunsheng Wang; Tiezhu An
Journal:  Proteome Sci       Date:  2015-06-27       Impact factor: 2.480

Review 9.  Reprogramming and development in nuclear transfer embryos and in interspecific systems.

Authors:  Patrick Narbonne; Kei Miyamoto; J B Gurdon
Journal:  Curr Opin Genet Dev       Date:  2012-10-11       Impact factor: 5.578

10.  Xenopus egg extract treatment reduced global DNA methylation of donor cells and enhanced somatic cell nuclear transfer embryo development in pigs.

Authors:  Xiaoyu Yang; Jiude Mao; Eric M Walters; Ming-Tao Zhao; Jennifer Teson; Kiho Lee; Randall S Prather
Journal:  Biores Open Access       Date:  2012-04
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