Multiple enhancers ensure precision of gap gene-expression patterns in the Drosophila embryo

被引:175
作者
Perry, Michael W. [4 ]
Boettiger, Alistair N. [3 ]
Levine, Michael [1 ,2 ]
机构
[1] Univ Calif Berkeley, Ctr Integrat Genom, Div Genet Genom & Dev, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Biophys Grad Grp, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Dept Integrat Biol, Berkeley, CA 94720 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
cis-regulation; development; robustness; TRANSCRIPTION FACTORS; REPRESSOR GRADIENTS; BODY PATTERN; BLASTODERM; MORPHOGEN; SYSTEM; HUNCHBACK; TRANSGENESIS; MELANOGASTER; ACTIVATION;
D O I
10.1073/pnas.1109873108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Segmentation of the Drosophila embryo begins with the establishment of spatially restricted gap gene-expression patterns in response to broad gradients of maternal transcription factors, such as Bicoid. Numerous studies have documented the fidelity of these expression patterns, even when embryos are subjected to genetic or environmental stress, but the underlying mechanisms for this transcriptional precision are uncertain. Here we present evidence that every gap gene contains multiple enhancers with overlapping activities to produce authentic patterns of gene expression. For example, a recently identified hunchback (hb) enhancer (located 5-kb upstream of the classic enhancer) ensures repression at the anterior pole. The combination of intronic and 5' knirps (kni) enhancers produces a faithful expression pattern, even though the intronic enhancer alone directs an abnormally broad expression pattern. We present different models for "enhancer synergy," whereby two enhancers with overlapping activities produce authentic patterns of gene expression.
引用
收藏
页码:13570 / 13575
页数:6
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