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本文引用的文献

1
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.
2
The zinc-finger protein Zelda is a key activator of the early zygotic genome in Drosophila.锌指蛋白泽尔达是果蝇早期合子基因组的关键激活因子。
Nature. 2008 Nov 20;456(7220):400-3. doi: 10.1038/nature07388. Epub 2008 Oct 19.
3
Shadow enhancers as a source of evolutionary novelty.作为进化新奇性来源的影子增强子。
Science. 2008 Sep 5;321(5894):1314. doi: 10.1126/science.1160631.
4
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.
5
Self-regulatory circuits in dorsoventral axis formation of the short-germ beetle Tribolium castaneum.短胚型甲虫赤拟谷盗背腹轴形成中的自我调节回路。
Dev Cell. 2008 Apr;14(4):605-15. doi: 10.1016/j.devcel.2008.02.011.
6
Analysis of the Tribolium homeotic complex: insights into mechanisms constraining insect Hox clusters.赤拟谷盗同源异型复合体的分析:对限制昆虫Hox基因簇机制的见解。
Dev Genes Evol. 2008 Apr;218(3-4):127-39. doi: 10.1007/s00427-008-0213-4. Epub 2008 Apr 8.
7
Evolution of the dorsal-ventral patterning network in the mosquito, Anopheles gambiae.冈比亚按蚊中背腹模式化网络的进化
Development. 2007 Jul;134(13):2415-24. doi: 10.1242/dev.02863. Epub 2007 May 23.
8
An optimized transgenesis system for Drosophila using germ-line-specific phiC31 integrases.一种利用生殖系特异性phiC31整合酶的果蝇优化转基因系统。
Proc Natl Acad Sci U S A. 2007 Feb 27;104(9):3312-7. doi: 10.1073/pnas.0611511104. Epub 2007 Feb 22.
9
A core transcriptional network for early mesoderm development in Drosophila melanogaster.果蝇早期中胚层发育的核心转录网络。
Genes Dev. 2007 Feb 15;21(4):436-49. doi: 10.1101/gad.1509007.
10
Whole-genome ChIP-chip analysis of Dorsal, Twist, and Snail suggests integration of diverse patterning processes in the Drosophila embryo.对背腹因子、扭曲蛋白和蜗牛蛋白进行全基因组芯片分析,结果表明果蝇胚胎中多种模式形成过程存在整合现象。
Genes Dev. 2007 Feb 15;21(4):385-90. doi: 10.1101/gad.1509607.

不同昆虫中增强子位置的保守性。

Conservation of enhancer location in divergent insects.

作者信息

Cande Jessica, Goltsev Yury, Levine Michael S

机构信息

Division of Genetics, Genomics and Development, Department of Molecular and Cell Biology, Center for Integrative Biology, University of California, Berkeley, CA 94720-3200, USA.

出版信息

Proc Natl Acad Sci U S A. 2009 Aug 25;106(34):14414-9. doi: 10.1073/pnas.0905754106. Epub 2009 Aug 3.

DOI:10.1073/pnas.0905754106
PMID:19666595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2732830/
Abstract

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.

摘要

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。