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A fragment of engrailed regulatory DNA can mediate transvection of the white gene in Drosophila.
Kassis, J A; VanSickle, E P; Sensabaugh, S M.
Afiliação
  • Kassis JA; Laboratory of Cellular and Molecular Biology, Food and Drug Administration, Bethesda, Maryland 20892.
Genetics ; 128(4): 751-61, 1991 Aug.
Article em En | MEDLINE | ID: mdl-1655566
ABSTRACT
We have found a fragment of engrailed regulatory DNA that has an unusual effect on expression of a linked marker gene, white, in the P element transposon CaSpeR. Normally, flies homozygous for a given CaSpeR insertion have darker eyes than heterozygotes. However, when a particular engrailed DNA fragment is included in that transposon, homozygotes often have lighter eyes than heterozygotes. Thus, engrailed DNA appears to cause white expression to be repressed in homozygotes. The suppression of white is dependent on the proximity of the two transposons in the genome-either in cis (i.e., on the same chromosome) or in trans (i.e., on homologous chromosomes). Thus, the engrailed fragment is mediating a phenomenon similar to that mediated by the zeste gene at the white locus. However, the interactions we observe do not require, nor are influenced by, mutations of zeste. We suggest that the engrailed DNA contains one or more binding sites for a protein that facilitates interactions between transposons. The normal function of these sites may be to mediate interactions between distant cis-regulatory regions of engrailed, a large locus that extends over 70 kilobases.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pigmentação / Sequências Reguladoras de Ácido Nucleico / Regulação da Expressão Gênica / Drosophila Limite: Animals Idioma: En Ano de publicação: 1991 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pigmentação / Sequências Reguladoras de Ácido Nucleico / Regulação da Expressão Gênica / Drosophila Limite: Animals Idioma: En Ano de publicação: 1991 Tipo de documento: Article