Moreno Tanya A, Jappelli Roberto, Izpisúa Belmonte Juan Carlos, Kintner Chris
The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.
Dev Biol. 2008 Mar 15;315(2):317-30. doi: 10.1016/j.ydbio.2007.12.038. Epub 2008 Jan 3.
The Mesp bHLH genes play a conserved role during segmental patterning of the mesoderm in the vertebrate embryo by specifying segmental boundaries and anteroposterior (A-P) segmental polarity. Here we use a xenotransgenic approach to compare the transcriptional enhancers that drive expression of the Mesp genes within segments of the presomitic mesoderm (PSM) of different vertebrate species. We find that the genomic sequences upstream of the mespb gene in the pufferfish Takifugu rubripes (Tr-mespb) are able to drive segmental expression in transgenic Xenopus embryos while those from the Xenopus laevis mespb (Xl-mespb) gene drive segmental expression in transgenic zebrafish. In both cases, the anterior segmental boundary of transgene expression closely matches the expression of the endogenous Mesp genes, indicating that many inputs into segmental gene expression are highly conserved. By contrast, we find that direct retinoic acid (RA) regulation of endogenous Mesp gene expression is variable among vertebrate species. Both Tr-mespb and Xl-mespb are directly upregulated by RA, through a complex, distal element. By contrast, RA represses the zebrafish Mesp genes. We show that this repression is mediated, in part, by RA-mediated activation of the Ripply genes, which together with Mesp genes form an RA-responsive negative feedback loop. These observations suggest that variations in a direct response to RA input may allow for changes in A-P patterning of the segments in different vertebrate species.
Mesp bHLH基因在脊椎动物胚胎中胚层的节段模式形成过程中发挥着保守作用,通过确定节段边界和前后(A-P)节段极性来实现。在这里,我们采用异种转基因方法来比较驱动不同脊椎动物物种体节中胚层(PSM)节段内Mesp基因表达的转录增强子。我们发现,河豚红鳍东方鲀(Tr-mespb)中mespb基因上游的基因组序列能够驱动转基因非洲爪蟾胚胎中的节段表达,而非洲爪蟾(Xl-mespb)基因的序列则能驱动转基因斑马鱼中的节段表达。在这两种情况下,转基因表达的前段边界与内源性Mesp基因的表达紧密匹配,这表明节段基因表达的许多输入因素是高度保守的。相比之下,我们发现内源性Mesp基因表达的直接视黄酸(RA)调控在脊椎动物物种之间存在差异。Tr-mespb和Xl-mespb都通过一个复杂的远端元件被RA直接上调。相反,RA抑制斑马鱼的Mesp基因。我们表明,这种抑制部分是由RA介导的Ripply基因激活所介导的,Ripply基因与Mesp基因一起形成了一个RA反应性负反馈环。这些观察结果表明,对RA输入的直接反应的变化可能允许不同脊椎动物物种节段的A-P模式发生改变。