Cande Jessica, Goltsev Yury, Levine Michael S
Division of Genetics, Genomics and Development, Department of Molecular and Cell Biology, Center for Integrative Biology, University of California, Berkeley, CA 94720-3200, USA.
Proc Natl Acad Sci U S A. 2009 Aug 25;106(34):14414-9. doi: 10.1073/pnas.0905754106. Epub 2009 Aug 3.
Dorsoventral (DV) patterning of the Drosophila embryo is controlled by a concentration gradient of Dorsal, a sequence-specific transcription factor related to mammalian NF-kappaB. The Dorsal gradient generates at least 3 distinct thresholds of gene activity and tissue specification by the differential regulation of target enhancers containing distinctive combinations of binding sites for Dorsal, Twist, Snail, and other DV determinants. To understand the evolution of DV patterning mechanisms, we identified and characterized Dorsal target enhancers from the mosquito Anopheles gambiae and the flour beetle Tribolium castaneum. Putative orthologous enhancers are located in similar positions relative to the target genes they control, even though they lack sequence conservation and sometimes produce divergent patterns of gene expression. The most dramatic example of this conservation is seen for the "shadow" enhancer regulating brinker: It is conserved within the intron of the neighboring Atg5 locus of both flies and mosquitoes. These results suggest that, like exons, an enhancer position might be subject to constraint. Thus, novel patterns of gene expression might arise from the modification of conserved enhancers rather than the invention of new ones. We propose that this enhancer constancy might be a general property of regulatory evolution, and should facilitate enhancer discovery in nonmodel organisms.
果蝇胚胎的背腹(DV)模式形成由背蛋白的浓度梯度控制,背蛋白是一种与哺乳动物核因子-κB相关的序列特异性转录因子。背蛋白梯度通过对含有背蛋白、扭曲蛋白、蜗牛蛋白和其他DV决定因素独特结合位点组合的靶增强子的差异调节,产生至少3个不同的基因活性和组织特化阈值。为了理解DV模式形成机制的进化,我们从冈比亚按蚊和赤拟谷盗中鉴定并表征了背蛋白靶增强子。尽管推定的直系同源增强子缺乏序列保守性,有时还会产生不同的基因表达模式,但它们相对于所控制的靶基因位于相似的位置。这种保守性最显著的例子见于调控边缘蛋白的“影子”增强子:它在果蝇和蚊子相邻的自噬相关蛋白5(Atg5)基因座的内含子中保守。这些结果表明,与外显子一样,增强子位置可能受到限制。因此,新的基因表达模式可能源于保守增强子的修饰而非新增强子的发明。我们提出,这种增强子恒定性可能是调控进化的一个普遍特性,并且应该有助于在非模式生物中发现增强子。