Structural Rules and Complex Regulatory Circuitry Constrain Expression of a Notch- and EGFR-Regulated Eye Enhancer

被引:121
作者
Swanson, Christina I. [1 ]
Evans, Nicole C. [1 ]
Barolo, Scott [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
PHOTORECEPTOR CELL FATES; PRIMARY PIGMENT-CELLS; DROSOPHILA EYE; GENE-EXPRESSION; PROMOTER; TRANSCRIPTION; SPECIFICATION; EVOLUTION; RECEPTOR; ELEMENTS;
D O I
10.1016/j.devcel.2009.12.026
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Enhancers integrate spatiotemporal information to generate precise patterns of gene expression. How complex is the regulatory logic of a typical developmental enhancer, and how important is its internal organization? Here, we examine in detail the structure and function of sparkling, a Notch- and EGFR/MAPK-regulated, cone cell-specific enhancer of the Drosophila Pax2 gene, in vivo. In addition to its 12 previously identified protein-binding sites, sparkling is densely populated with previously unmapped regulatory sequences, which interact in complex ways to control gene expression. One segment is essential for activation at a distance, yet dispensable for other activation functions and for cell type patterning. Unexpectedly, rearranging sparkling's regulatory sites converts it into a robust photoreceptor-specific enhancer. Our results show that a single combination of regulatory inputs can encode multiple outputs, and suggest that the enhancer's organization determines the correct expression pattern by facilitating certain short-range regulatory interactions at the expense of others.
引用
收藏
页码:359 / 370
页数:12
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