Document Detail


Somatic nucleus reprogramming is significantly improved by m-carboxycinnamic acid bishydroxamide, a histone deacetylase inhibitor.
MedLine Citation:
PMID:  20566633     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Somatic cell nuclear transfer (SCNT) has shown tremendous potential for understanding the mechanisms of reprogramming and creating applications in the realms of agriculture, therapeutics, and regenerative medicine, although the efficiency of reprogramming is still low. Somatic nucleus reprogramming is triggered in the short time after transfer into recipient cytoplasm, and therefore, this period is regarded as a key stage for optimizing SCNT. Here we report that CBHA, a histone deacetylase inhibitor, modifies the acetylation status of somatic nuclei and increases the developmental potential of mouse cloned embryos to reach pre- and post-implantation stages. Furthermore, the cloned embryos treated by CBHA displayed higher efficiency in the derivation of nuclear transfer embryonic stem cell lines by promoting outgrowths. More importantly, CBHA increased blastocyst quality compared with trichostatin A, another prevalent histone deacetylase inhibitor reported previously. Use of CBHA should improve the productivity of SCNT for a variety of research and clinical applications, and comparisons of cells with different levels of pluripotency and treated with CBHA versus trichostatin A will facilitate studies of the mechanisms of reprogramming.
Authors:
Xiangpeng Dai; Jie Hao; Xiao-Jun Hou; Tang Hai; Yong Fan; Yang Yu; Alice Jouneau; Liu Wang; Qi Zhou
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2010-06-21
Journal Detail:
Title:  The Journal of biological chemistry     Volume:  285     ISSN:  1083-351X     ISO Abbreviation:  J. Biol. Chem.     Publication Date:  2010 Oct 
Date Detail:
Created Date:  2010-09-27     Completed Date:  2010-10-26     Revised Date:  2012-05-07    
Medline Journal Info:
Nlm Unique ID:  2985121R     Medline TA:  J Biol Chem     Country:  United States    
Other Details:
Languages:  eng     Pagination:  31002-10     Citation Subset:  IM    
Affiliation:
State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
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MeSH Terms
Descriptor/Qualifier:
Acetylation
Animals
Blastocyst / cytology,  metabolism*
Cell Dedifferentiation / drug effects*
Cell Nucleus / metabolism*
Cinnamates / pharmacology*
Cloning, Organism*
Female
Histone Deacetylase Inhibitors / pharmacology*
Hydroxamic Acids / pharmacology
Male
Mice
Mice, Inbred ICR
Nuclear Transfer Techniques
Chemical
Reg. No./Substance:
0/Cinnamates; 0/Histone Deacetylase Inhibitors; 0/Hydroxamic Acids; 0/carboxycinnamic acid bishydroxamide; 58880-19-6/trichostatin A
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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