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Identification of a compound origin of replication at the HMR-E locus in Saccharomyces cerevisiae.
Hurst, S T; Rivier, D H.
Afiliación
  • Hurst ST; Department of Cell and Structural Biology, University of Illinois, Urbana-Champaign, Urbana, Illinois 61801, USA.
J Biol Chem ; 274(7): 4155-9, 1999 Feb 12.
Article en En | MEDLINE | ID: mdl-9933610
ABSTRACT
Eukaryotic chromosomal origins of replication are best defined in Saccharomyces cerevisiae. Previous analysis of yeast origins suggests that they are relatively simple structures comprised of three or four small DNA sequence elements contained within approximately 100-200-base pair regions (Gilbert, D. M. (1998) Curr. Opin. Genet. Dev. 8, 194-199). In contrast, the sequence elements that may comprise origins in multicellular eukaryotes are largely unknown. The yeast HMR-E region is both a chromosomal origin of replication and a silencer that represses transcription of adjacent genes through a position effect. The analysis presented here indicated that HMR-E had a novel DNA structure that was more complex than defined for other yeast origins, and thus revealed that there is variation in the structural complexity of yeast origins. In contrast to "simple" yeast origins, the origin at HMR-E consisted of at least three independent subregions that had the capacity to initiate replication. We have termed HMR-E a compound origin to reflect its structural complexity. Furthermore, only one origin within the compound origin was a silencer.
Asunto(s)
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Banco de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Regulación Fúngica de la Expresión Génica / Secuencias Reguladoras de Ácidos Nucleicos / Origen de Réplica / Replicación del ADN Tipo de estudio: Diagnostic_studies Idioma: En Año: 1999 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Regulación Fúngica de la Expresión Génica / Secuencias Reguladoras de Ácidos Nucleicos / Origen de Réplica / Replicación del ADN Tipo de estudio: Diagnostic_studies Idioma: En Año: 1999 Tipo del documento: Article