Literature DB >> 17287828

Nuclear reprogramming: the strategy used in normal development is also used in somatic cell nuclear transfer and parthenogenesis.

Tianlong Gao1, Junke Zheng, Fengying Xing, Haiyan Fang, Feng Sun, Ayong Yan, Xun Gong, Hui Ding, Fan Tang, Hui Z Sheng.   

Abstract

Somatic cell nuclear transfer (SCNT) and parthenogenesis are alternative forms of reproduction and development, building new life cycles on differentiated somatic cell nuclei and duplicated maternal chromatin, respectively. In the preceding paper (Sun F, et al., Cell Res 2007; 17:117-134.), we showed that an "erase-and-rebuild" strategy is used in normal development to transform the maternal gene expression profile to a zygotic one. Here, we investigate if the same strategy also applies to SCNT and parthenogenesis. The relationship between chromatin and chromatin factors (CFs) during SCNT and parthenogenesis was examined using immunochemical and GFP-fusion protein assays. Results from these studies indicated that soon after nuclear transfer, a majority of CFs dissociated from somatic nuclei and were redistributed to the cytoplasm of the egg. The erasure process in oogenesis is recaptured during the initial phase in SCNT. Most CFs entered pseudo-pronuclei shortly after their formation. In parthenogenesis, all parthenogenotes underwent normal oogenesis, and thus had removed most CFs from chromosomes before the initiation of development. The CFs were subsequently re-associated with female pronuclei in time and sequence similar to that in fertilized embryos. Based on these data, we conclude that the "erase-and-rebuild" process observed in normal development also occurs in SCNT and in parthenogenesis, albeit in altered fashions. The process is responsible for transcription reprogramming in these procedures. The "erase" process in SCNT is compressed and the efficiency is compromised, which likely contribute to the developmental defects often observed in nuclear transfer (nt) embryos. Furthermore, results from this study indicated that the cytoplasm of an egg contains most, if not all, essential components for assembling the zygotic program and can assemble them onto appropriate diploid chromatin of distinct origins.

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Year:  2007        PMID: 17287828     DOI: 10.1038/cr.2007.2

Source DB:  PubMed          Journal:  Cell Res        ISSN: 1001-0602            Impact factor:   25.617


  9 in total

1.  Recipient cell nuclear factors are required for reprogramming by nuclear transfer.

Authors:  Dieter Egli; Kevin Eggan
Journal:  Development       Date:  2010-05-12       Impact factor: 6.868

2.  Transient Dux expression facilitates nuclear transfer and induced pluripotent stem cell reprogramming.

Authors:  Lei Yang; Xuefei Liu; Lishuang Song; Anqi Di; Guanghua Su; Chunling Bai; Zhuying Wei; Guangpeng Li
Journal:  EMBO Rep       Date:  2020-07-27       Impact factor: 8.807

3.  Transient JMJD2B-mediated reduction of H3K9me3 levels improves reprogramming of embryonic stem cells into cloned embryos.

Authors:  Jisha Antony; Fleur Oback; Larry W Chamley; Björn Oback; Götz Laible
Journal:  Mol Cell Biol       Date:  2012-12-21       Impact factor: 4.272

Review 4.  Mechanisms of nuclear reprogramming by eggs and oocytes: a deterministic process?

Authors:  Jerome Jullien; Vincent Pasque; Richard P Halley-Stott; Kei Miyamoto; J B Gurdon
Journal:  Nat Rev Mol Cell Biol       Date:  2011-06-23       Impact factor: 94.444

5.  Epigenetic modification with trichostatin A does not correct specific errors of somatic cell nuclear transfer at the transcriptomic level; highlighting the non-random nature of oocyte-mediated reprogramming errors.

Authors:  Sayyed Morteza Hosseini; Isabelle Dufort; Julie Nieminen; Fariba Moulavi; Hamid Reza Ghanaei; Mahdi Hajian; Farnoosh Jafarpour; Mohsen Forouzanfar; Hamid Gourbai; Abdol Hossein Shahverdi; Mohammad Hossein Nasr-Esfahani; Marc-André Sirard
Journal:  BMC Genomics       Date:  2016-01-04       Impact factor: 3.969

6.  TFIIB co-localizes and interacts with α-tubulin during oocyte meiosis in the mouse and depletion of TFIIB causes arrest of subsequent embryo development.

Authors:  Hui Liu; Feng-Xia Yin; Chun-Ling Bai; Qi-Yuan Shen; Zhu-Ying Wei; Xin-Xin Li; Hao Liang; Shorgan Bou; Guang-Peng Li
Journal:  PLoS One       Date:  2013-11-14       Impact factor: 3.240

7.  Development to term of cloned cattle derived from donor cells treated with valproic acid.

Authors:  Juliano Rodrigues Sangalli; Marcos Roberto Chiaratti; Tiago Henrique Camara De Bem; Reno Roldi de Araújo; Fabiana Fernandes Bressan; Rafael Vilar Sampaio; Felipe Perecin; Lawrence Charles Smith; Willian Allan King; Flávio Vieira Meirelles
Journal:  PLoS One       Date:  2014-06-24       Impact factor: 3.240

8.  KDM4B-mediated reduction of H3K9me3 and H3K36me3 levels improves somatic cell reprogramming into pluripotency.

Authors:  Jingwei Wei; Jisha Antony; Fanli Meng; Paul MacLean; Rebekah Rhind; Götz Laible; Björn Oback
Journal:  Sci Rep       Date:  2017-08-08       Impact factor: 4.379

9.  Nuclear reprogramming of sperm and somatic nuclei in eggs and oocytes.

Authors:  Marta Teperek; Kei Miyamoto
Journal:  Reprod Med Biol       Date:  2013-06-04
  9 in total

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