Journal article
De novo synthesis of DNA in human platelets
Archives of biochemistry and biophysics, v 226(1)
1983
PMID: 6639052
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
Platelets, incubated with radiolabeled thymidine and purified free of contaminating nucleated cells, were analyzed for their ability to synthesize DNA. The only DNA species isolated from these purified platelets was mitochondrial DNA. The CsCl gradient-purified platelet DNA was treated with the restriction endonucleases
EcoRI,
HindIII and
HpaI yielding the expected pattern for human mitochondrial DNA. Nitrocellulose blots of the electrophoresed, restriction endonuclease-treated DNA were fluorographed. All of the DNA fragments generated by the restriction enzymes were labeled, indicating
de novo synthesis. This was further substantiated by inhibition of DNA synthesis by ethidium bromide and 2′,3′-dideoxythymidine. Platelet DNA appeared to become greatly fragmented after 4 to 7 days storage while all of the thymidine incorporated was observed in intact mitochondrial DNA. These results indicate a continuous degradation of platelet mitochondrial DNA with no apparent repair mechanism. The ability of platelets to synthesize DNA may be associated with the protein synthetic capacity of platelets previously described.
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Details
- Title
- De novo synthesis of DNA in human platelets
- Creators
- Gerald Soslau - Hahnemann University Hospital
- Publication Details
- Archives of biochemistry and biophysics, v 226(1)
- Publisher
- Elsevier
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- [Retired Faculty]
- Web of Science ID
- WOS:A1983RL61100027
- Scopus ID
- 2-s2.0-0020605146
- Other Identifier
- 991019183989804721
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InCites Highlights
Data related to this publication, from InCites Benchmarking & Analytics tool:
- Web of Science research areas
- Biochemistry & Molecular Biology
- Biophysics