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Physical mapping of an early sea urchin gene battery from Parenchinus angulosus

Bibliography: pages 95-99.

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Bibliographic Details
Main Author: Lawson, T N
Other Authors: Sewell, Bryan Trevor
Format: Thesis
Language:English
Published: Department of Molecular and Cell Biology 2016
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access_status_str Open Access
author Lawson, T N
author2 Sewell, Bryan Trevor
author_browse Lawson, T N
Sewell, Bryan Trevor
author_facet Sewell, Bryan Trevor
Lawson, T N
author_sort Lawson, T N
collection Thesis
description Bibliography: pages 95-99.
format Thesis
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institution University of Cape Town (South Africa)
language eng
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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:11427/17701 Physical mapping of an early sea urchin gene battery from Parenchinus angulosus Lawson, T N Sewell, Bryan Trevor Von Holt, Claus Sea-urchins - Genetics Bibliography: pages 95-99. The aim of this project was to characterise an early histone gene battery isolated from Parenchinus angulosus. An early histone gene battery (named H27) which was believed to have been isolated from Parenchinus angulosus, appeared by restriction enzyme mapping and partial sequencing to be identical to H22, an early histone gene battery isolated from Psammechinus miliaris. (This latter gene was obtained from M. Birnstiel.) This was further confirmed by electron microscopy, and proved to be a convenient testing ground for the electron microscopic techniques of denaturation mapping and heteroduplex anlysis. Another gene battery (named SU1) isolated fromParenchinus angulosus, was then characterised using the techniques developed whilst studying H27. The restriction enzyme map of this clone is different to that of H22, indicating that differences do indeed exist between these two early histone gene batteries. SU1 also showed the expected order of the five histone genes, as determined by hybridization against the coding regions of H22. The denaturation map of SU1 showed AT rich spacer regions and GC rich coding regions. Heteroduplex analysis indicated that the spacer regions between the Hl and H2A, the H2A and H3, and the H3 and the H2B gene coding areas are essentially nonhomologous. The H4 structural gene and corresponding spacer regions were not included in this analysis. Because it is known that all the five histones are coded for on the same strand of DNA in H22, and that each of the genes is transcribed in the same direction, it follows that, the same holds for, at least, the Hl, H2A, H3 and H2B genes of SU1. 2016-03-14T07:14:48Z 2016-03-14T07:14:48Z 1988 Master Thesis Masters MSc http://hdl.handle.net/11427/17701 eng application/pdf Department of Molecular and Cell Biology Faculty of Science University of Cape Town
spellingShingle Sea-urchins - Genetics
Lawson, T N
Physical mapping of an early sea urchin gene battery from Parenchinus angulosus
thesis_degree_str Master's
title Physical mapping of an early sea urchin gene battery from Parenchinus angulosus
title_full Physical mapping of an early sea urchin gene battery from Parenchinus angulosus
title_fullStr Physical mapping of an early sea urchin gene battery from Parenchinus angulosus
title_full_unstemmed Physical mapping of an early sea urchin gene battery from Parenchinus angulosus
title_short Physical mapping of an early sea urchin gene battery from Parenchinus angulosus
title_sort physical mapping of an early sea urchin gene battery from parenchinus angulosus
topic Sea-urchins - Genetics
url http://hdl.handle.net/11427/17701
work_keys_str_mv AT lawsontn physicalmappingofanearlyseaurchingenebatteryfromparenchinusangulosus