Source:http://linkedlifedata.com/resource/pubmed/id/11473545
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2001-7-27
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pubmed:abstractText |
The present study examines the effects on embryogenesis of microinjecting Xenopus laevis fertilized eggs with 5-aza-2'-deoxycytidine (5-Aza-CdR), which induces hypomethylation of DNA, and 5-methyl-2'- deoxycytidine-5'-triphosphate (5-methyl-dCTP), which induces hypermethylation of DNA. Embryos injected with either one of these analogs cleaved normally until the mid-blastula stage, but underwent massive cell dissociation and stopped development at the early gastrula stage. Dissociated cells that appeared here were positive by terminal deoxyribonucleotidyl transferase-mediated deoxyuridine triphosphate-digoxigenin nick end-labeling and contained fragmented nuclei with condensed chromatin. The DNA from these cells formed a "ladder" on electrophoresis. Furthermore, the induction of cell dissociation by 5-Aza-CdR and 5-methyl-dCTP was postponed by 2-3 h by co-injection of Bcl-2 mRNA and the normal metabolite (CdR and dCTP, respectively). Using a specific antibody against 5-methyl-cytosine, we confirmed that 5-Aza-CdR induces hypomethylation, whereas 5-methyl-dCTP induces hypermethylation in X. laevis embryos before the onset of cell dissociation. Incorporation of radioactive precursors revealed that synthesis of DNA, and also RNA, is inhibited significantly in both 5-Aza-CdR-injected and 5-methyl-dCTP-injected embryos. These results show that 5-Aza-CdR and 5-methyl-dCTP are incorporated into DNA and induce apoptosis, probably through alteration of DNA methylation coupled with inhibition of DNA replication and/or transcription.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/5-methyldeoxycytidine,
http://linkedlifedata.com/resource/pubmed/chemical/Azacitidine,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Modification Methylases,
http://linkedlifedata.com/resource/pubmed/chemical/Deoxycytidine,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-bcl-2,
http://linkedlifedata.com/resource/pubmed/chemical/decitabine
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0012-1592
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
383-90
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pubmed:dateRevised |
2006-5-5
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pubmed:meshHeading |
pubmed-meshheading:11473545-Animals,
pubmed-meshheading:11473545-Apoptosis,
pubmed-meshheading:11473545-Azacitidine,
pubmed-meshheading:11473545-DNA Fragmentation,
pubmed-meshheading:11473545-DNA Methylation,
pubmed-meshheading:11473545-DNA Modification Methylases,
pubmed-meshheading:11473545-Deoxycytidine,
pubmed-meshheading:11473545-Embryo, Nonmammalian,
pubmed-meshheading:11473545-Female,
pubmed-meshheading:11473545-In Situ Nick-End Labeling,
pubmed-meshheading:11473545-Microinjections,
pubmed-meshheading:11473545-Oocytes,
pubmed-meshheading:11473545-Proto-Oncogene Proteins c-bcl-2,
pubmed-meshheading:11473545-Xenopus laevis
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pubmed:year |
2001
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pubmed:articleTitle |
Activation of the maternally preset program of apoptosis by microinjection of 5-aza-2'-deoxycytidine and 5-methyl-2'-deoxycytidine-5'-triphosphate in Xenopus laevis embryos.
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pubmed:affiliation |
Laboratory of Molecular Embryology, Department of Biological Sciences, Graduate School of Science, University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
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pubmed:publicationType |
Journal Article
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