drosophila mulleri
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2011 ◽  
Vol 47 (1) ◽  
pp. 161-162
Author(s):  
G. S. Shakirzyanova ◽  
A. P. Khuzhakulov ◽  
S. I. Kukanova ◽  
V. S. Abdukakharov

ChemInform ◽  
2001 ◽  
Vol 32 (19) ◽  
pp. no-no
Author(s):  
G. Yu. Ishmuratov ◽  
R. Ya. Kharisov ◽  
O. V. Botsman ◽  
V. V. Zorin ◽  
G. A. Tolstikov

Genetics ◽  
1992 ◽  
Vol 132 (4) ◽  
pp. 1071-1079
Author(s):  
D Falb ◽  
J Fischer ◽  
T Maniatis

Abstract The Adh-2 gene of Drosophila mulleri is expressed in the larval fat body and the adult fat body and hindgut, and a 1500-bp element located 2-3 kb upstream of the Adh-2 promoter is necessary for maximal levels of transcription. Previous work demonstrated that deletion of sequences between this upstream element and the Adh-2 promoter results in Adh-2 gene expression in a novel larval tissue, the middle midgut. In this study we show that the upstream element possesses all of the characteristics of a transcriptional enhancer: its activity is independent of orientation, it acts on a heterologous promoter, and it functions at various positions both 5' and 3' to the Adh-2 gene. Full enhancer function can be localized to a 750-bp element, although other regions possess some redundant activity. The ectopic expression pattern is dependent on the proximity of at least two sequence elements. Thus, tissue-specific transcription can involve complex proximity-dependent interactions among combinations of regulatory elements.


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