Sharpe J, Nonchev S, Gould A, Whiting J, Krumlauf R
Division of Developmental Neurobiology, National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK.
EMBO J. 1998 Mar 16;17(6):1788-98. doi: 10.1093/emboj/17.6.1788.
The clustered organisation of Hox complexes is highly conserved in vertebrates and the reasons for this are believed to be linked with the regulatory mechanisms governing their expression. In analysis of the Hoxb4-Hoxb6 region of the HoxB complex we identified enhancers which lie in the intergenic region between Hoxb4 and Hoxb5, and which are capable of mediating the correct boundaries of neural and mesodermal expression for Hoxb5. We examined their regulatory properties in the context of the local genomic region spanning the two genes by transgenic analysis, in which each promoter was independently marked with a different reporter, to monitor simultaneously the relative transcriptional read-outs from each gene. Our analysis revealed that within this intergenic region: (i) a limb and a neural enhancer selectively activate Hoxb4 as opposed to Hoxb5; (ii) a separate neural enhancer is able to activate both genes, but expression is dependent upon competition between the two promoters for the enhancer and is influenced by the local genomic context; (iii) mesodermal enhancer activities can be shared between the genes. We found similar types of regulatory interactions between Hoxb5 and Hoxb6. Together these results provide evidence for three separate general mechanisms: selectivity, competition and sharing, that control the balance of cis-regulatory interactions necessary for generating the proper spatial and temporal patterns of Hox gene expression. We suggest that these mechanisms are part of a regulatory basis for maintenance of Hox organisation.
Hox基因复合体的簇状组织在脊椎动物中高度保守,其原因被认为与调控它们表达的机制有关。在对HoxB复合体的Hoxb4-Hoxb6区域进行分析时,我们鉴定出了位于Hoxb4和Hoxb5之间基因间区域的增强子,这些增强子能够介导Hoxb5在神经和中胚层表达的正确边界。我们通过转基因分析在跨越这两个基因的局部基因组区域背景下研究了它们的调控特性,在转基因分析中,每个启动子都用不同的报告基因独立标记,以同时监测每个基因的相对转录输出。我们的分析表明,在这个基因间区域内:(i)一个肢体和一个神经增强子选择性地激活Hoxb4而非Hoxb5;(ii)一个单独的神经增强子能够激活这两个基因,但表达取决于两个启动子对增强子的竞争,并受局部基因组背景的影响;(iii)中胚层增强子活性可以在这两个基因之间共享。我们在Hoxb5和Hoxb6之间发现了类似类型的调控相互作用。这些结果共同为三种不同的一般机制提供了证据:选择性、竞争性和共享性,它们控制着产生Hox基因表达的正确时空模式所需的顺式调控相互作用的平衡。我们认为这些机制是维持Hox组织的调控基础的一部分。