Suboptimization of developmental enhancers

被引:219
作者
Farley, Emma K. [1 ,2 ]
Olson, Katrina M. [1 ,2 ]
Zhang, Wei [3 ]
Brandt, Alexander J. [4 ]
Rokhsar, Daniel S. [1 ]
Levine, Michael S. [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Div Genet Genom & Dev, Ctr Integrat Genom, Berkeley, CA 94720 USA
[2] Princeton Univ, Lewis Sigler Inst Integrat Genom, Princeton, NJ 08544 USA
[3] Univ Calif San Diego, Dept Med, San Diego, CA 92093 USA
[4] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
关键词
TRANSCRIPTION FACTORS; SIGNALING ESTABLISHES; SUPER-ENHANCERS; MATERNAL GATA; CELL IDENTITY; EYE ENHANCER; NEURAL-TUBE; DNA; COMPLEX; ETS;
D O I
10.1126/science.aac6948
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
Transcriptional enhancers direct precise on-off patterns of gene expression during development. To explore the basis for this precision, we conducted a high-throughput analysis of the Otx-a enhancer, which mediates expression in the neural plate of Ciona embryos in response to fibroblast growth factor (FGF) signaling and a localized GATA determinant. We provide evidence that enhancer specificity depends on submaximal recognition motifs having reduced binding affinities ("suboptimization"). Native GATA and ETS (FGF) binding sites contain imperfect matches to consensus motifs. Perfect matches mediate robust but ectopic patterns of gene expression. The native sites are not arranged at optimal intervals, and subtle changes in their spacing alter enhancer activity. Multiple tiers of enhancer suboptimization produce specific, but weak, patterns of expression, and we suggest that clusters of weak enhancers, including certain "superenhancers," circumvent this trade-off in specificity and activity.
引用
收藏
页码:325 / 328
页数:4
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