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Deoxyribonuclease probing on sea urchin embryo chromatin

Bibliography: pages 118-143.

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Main Author: Landsman, David
Format: Thesis
Language:English
Published: Department of Molecular and Cell Biology 2016
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access_status_str Open Access
author Landsman, David
author_browse Landsman, David
author_facet Landsman, David
author_sort Landsman, David
collection Thesis
description Bibliography: pages 118-143.
format Thesis
id oai:open.uct.ac.za:11427/17600
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:31:43.046Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2016
publishDateRange 2016
publishDateSort 2016
publisher Department of Molecular and Cell Biology
publisherStr Department of Molecular and Cell Biology
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source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/17600 Deoxyribonuclease probing on sea urchin embryo chromatin Landsman, David Biochemistry Bibliography: pages 118-143. The role that the sea urchin, Parechinus angulosus, embryo and sperm histone variants play in chromatin structure has been investigated. Chromatin structure has been determined at different levels of resolution in sperm and in developing embryos using micrococcal nuclease, pancreatic deoxyribonuclease (DNase I) and restriction endonucleases. Micrococcal nuclease and restriction endonuclease digestions of sea urchin gastrula chromatin have been analysed and it is shown that it is not possible to isolate large polynucleosomal chromatin complexes which are soluble in low ionic strength buffers. The nucleosomal DNA repeat lengths for sea urchin blastula, gastrula and sperm have been determined using micrococcal nuclease. The repeat length for sperm is significantly larger than blastula and gastrula repeat lengths whereas blastula and gastrula repeat lengths are not significantly different. Nucleosomal core particles have been isolated from early blastula, gastrula and sperm of sea urchins. After DNase I digestion of 51-labelled core particles the rate constants of cutting of the DNA at the susceptible sites on these core particles have been determined. The DNase I digestion kinetics of blastula and gastrula core particles are similar whereas sperm core particles are digested at a slower rate, mainly at the sites which are closest to the ends of the core particle DNA. Also, a site, which is 5 bases on the outside of the core particle and which is partially protected from nuclease attack, has been identified. The implications of these findings in relation to the histone variants in embryos and sperm of sea urchins are discussed. 2016-03-09T09:05:51Z 2016-03-09T09:05:51Z 1983 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/17600 eng application/pdf Department of Molecular and Cell Biology Faculty of Science University of Cape Town
spellingShingle Biochemistry
Landsman, David
Deoxyribonuclease probing on sea urchin embryo chromatin
thesis_degree_str Doctoral
title Deoxyribonuclease probing on sea urchin embryo chromatin
title_full Deoxyribonuclease probing on sea urchin embryo chromatin
title_fullStr Deoxyribonuclease probing on sea urchin embryo chromatin
title_full_unstemmed Deoxyribonuclease probing on sea urchin embryo chromatin
title_short Deoxyribonuclease probing on sea urchin embryo chromatin
title_sort deoxyribonuclease probing on sea urchin embryo chromatin
topic Biochemistry
url http://hdl.handle.net/11427/17600
work_keys_str_mv AT landsmandavid deoxyribonucleaseprobingonseaurchinembryochromatin