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本文引用的文献

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Developing compound eye in lozenge mutants of Drosophila: lozenge expression in the R7 equivalence group.果蝇菱形突变体中复眼的发育:菱形基因在R7等效组中的表达
Dev Genes Evol. 1997 May;206(8):481-493. doi: 10.1007/s004270050079.
2
Determination of cell fates in the R7 equivalence group of the Drosophila eye by the concerted regulation of D-Pax2 and TTK88.通过D-Pax2和TTK88的协同调控来确定果蝇眼睛R7等效组中的细胞命运。
Dev Biol. 2009 Jul 1;331(1):68-77. doi: 10.1016/j.ydbio.2009.04.026. Epub 2009 May 3.
3
Hindsight modulates Delta expression during Drosophila cone cell induction.后见之明在果蝇视锥细胞诱导过程中调节Delta表达。
Development. 2009 Mar;136(6):975-82. doi: 10.1242/dev.027318.
4
Evolution acts on enhancer organization to fine-tune gradient threshold readouts.进化作用于增强子组织,以微调梯度阈值读数。
PLoS Biol. 2008 Nov 4;6(11):e263. doi: 10.1371/journal.pbio.0060263.
5
Regulation of estrogen receptor-mediated long range transcription via evolutionarily conserved distal response elements.通过进化保守的远端反应元件对雌激素受体介导的远程转录进行调控。
J Biol Chem. 2008 Nov 21;283(47):32977-88. doi: 10.1074/jbc.M802024200. Epub 2008 Aug 25.
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Analysis of homeodomain specificities allows the family-wide prediction of preferred recognition sites.对同源结构域特异性的分析能够实现全家族范围内对偏好识别位点的预测。
Cell. 2008 Jun 27;133(7):1277-89. doi: 10.1016/j.cell.2008.05.023.
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Sepsid even-skipped enhancers are functionally conserved in Drosophila despite lack of sequence conservation.脓毒症偶数跳过增强子在果蝇中功能保守,尽管缺乏序列保守性。
PLoS Genet. 2008 Jun 27;4(6):e1000106. doi: 10.1371/journal.pgen.1000106.
8
A positive role for NLI/Ldb1 in long-range beta-globin locus control region function.NLI/Ldb1在远距离β-珠蛋白基因座控制区功能中发挥的积极作用。
Mol Cell. 2007 Dec 14;28(5):810-22. doi: 10.1016/j.molcel.2007.09.025.
9
A directional recombination cloning system for restriction- and ligation-free construction of GFP, DsRed, and lacZ transgenic Drosophila reporters.一种用于无限制酶切和连接构建绿色荧光蛋白(GFP)、红色荧光蛋白(DsRed)和乳糖操纵子(lacZ)转基因果蝇报告基因的定向重组克隆系统。
Gene. 2008 Jan 31;408(1-2):180-6. doi: 10.1016/j.gene.2007.11.003. Epub 2007 Nov 21.
10
A novel promoter-tethering element regulates enhancer-driven gene expression at the bithorax complex in the Drosophila embryo.一种新型的启动子连接元件在果蝇胚胎的双胸复合体中调节增强子驱动的基因表达。
Development. 2008 Jan;135(1):123-31. doi: 10.1242/dev.010744. Epub 2007 Nov 28.

结构规则和复杂的调控回路限制了 Notch 和 EGFR 调节的眼睛增强子的表达。

Structural rules and complex regulatory circuitry constrain expression of a Notch- and EGFR-regulated eye enhancer.

机构信息

Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.

出版信息

Dev Cell. 2010 Mar 16;18(3):359-70. doi: 10.1016/j.devcel.2009.12.026.

DOI:10.1016/j.devcel.2009.12.026
PMID:20230745
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2847355/
Abstract

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.

摘要

增强子整合时空信息,以生成精确的基因表达模式。一个典型的发育增强子的调控逻辑有多复杂,其内部组织有多重要?在这里,我们详细研究了果蝇 Pax2 基因的 Notch 和 EGFR/MAPK 调节的锥形细胞特异性增强子 sparkling 的结构和功能。除了其之前鉴定的 12 个蛋白结合位点外,sparkling 还密集分布着以前未被映射的调控序列,这些序列以复杂的方式相互作用以控制基因表达。一个片段对于远距离激活是必需的,但对于其他激活功能和细胞类型模式形成是可有可无的。出乎意料的是,改变 sparkling 的调控位点将其转化为一种强大的光感受器特异性增强子。我们的结果表明,单个调控输入的组合可以编码多个输出,并且表明增强子的组织通过促进某些短程调控相互作用而牺牲其他相互作用来确定正确的表达模式。