White as a reporter gene to detect transcriptional silencers specifying position-specific gene expression during Drosophila melanogaster eye development

The white+ gene was used as a reporter to detect transcriptional silencer activity in the Drosophila genome. Changes in the spatial expression pattern of white were scored in the adult eye as nonuniform patterns of pigmentation. Thirty-six independent P[lacW] transposant lines were collected. These...

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Veröffentlicht in:Genetics (Austin) 1995-11, Vol.141 (3), p.1075-1086
Hauptverfasser: Sun, Y.H. (National Yang Ming University, Shipai Taipei, Taiwan, Republic of China.), Tsai, C.J, Green, M.M, Chao, J.L, Yu, C.T, Jaw, T.J, Yeh, J.Y, Bolshakov, V.N
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Sprache:eng
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Zusammenfassung:The white+ gene was used as a reporter to detect transcriptional silencer activity in the Drosophila genome. Changes in the spatial expression pattern of white were scored in the adult eye as nonuniform patterns of pigmentation. Thirty-six independent P[lacW] transposant lines were collected. These represent 12 distinct pigmentation patterns and probably 21 loci. The spatial pigmentation pattern is due to cis-acting suppression of white+ expression, and the suppression probably depends on cell position rather than cell type. The mechanism of suppression differs from inactivation by heterochromatin. In addition, activation of lacZ in P[lacW] occurs also in specific patterns in imaginal discs and embryos in many of the lines. The expression patterns of white+ and lacZ may reflect the activity of regulatory elements belonging to an endogenous gene near each P[lacW] insertion site. We speculate that these putative POSE (position-specific expression) genes may have a role in pattern formation of the eye as well as other imaginal structures. Three of the loci identified are optomotor-blind, engrailed and invected. teashirt is also implicated as a candidate gene. We propose that this "silencer trap" may be an efficient way of identifying genes involved in imaginal pattern formation
ISSN:0016-6731
1943-2631
1943-2631
DOI:10.1093/genetics/141.3.1075