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由 Hoxd 全局调控区驱动的附肢表达是一种古老的有颌类特征。

Appendage expression driven by the Hoxd Global Control Region is an ancient gnathostome feature.

机构信息

Department of Organismal Biology and Anatomy, University of Chicago, Chicago, IL 60637, USA.

出版信息

Proc Natl Acad Sci U S A. 2011 Aug 2;108(31):12782-6. doi: 10.1073/pnas.1109993108. Epub 2011 Jul 15.

Abstract

The evolutionary transition of the fins of fish into tetrapod limbs involved genetic changes to developmental systems that resulted in novel skeletal patterns and functions. Approaches to understanding this issue have entailed the search for antecedents of limb structure in fossils, genes, and embryos. Comparative genetic analyses have produced ambiguous results: although studies of posterior Hox genes from homology group 13 (Hoxa-13 and Hoxd-13) reveal similarities in gene expression between the distal segments of fins and limbs, this functional homology has not been supported by genomic comparisons of the activity of their cis-regulatory elements, namely the Hoxd Global Control Region. Here, we show that cis-regulatory elements driving Hoxd gene expression in distal limbs are present in fish. Using an interspecies transgenesis approach, we find functional conservation between gnathostome Hoxd enhancers, demonstrating that orthologous sequences from tetrapods, zebrafish and skate can drive reporter gene expression in mouse limbs and zebrafish fins. Our results support the notion that some of the novelties associated with tetrapod limbs arose by modification of deeply conserved cis- and trans-acting mechanisms of Hox regulation in gnathostomes.

摘要

鱼类的鳍演变成四足动物的肢体,涉及到发育系统的基因变化,导致了新的骨骼模式和功能。理解这个问题的方法包括在化石、基因和胚胎中寻找肢体结构的前身。比较遗传学分析得出的结果并不明确:尽管对同源异型盒基因 13 组(Hoxa-13 和 Hoxd-13)的后部基因进行了研究,揭示了鳍和肢体远端节段之间基因表达的相似性,但它们顺式调控元件(即 Hoxd 全局调控区)的活性的基因组比较并没有支持这种功能同源性。在这里,我们表明,驱动远端肢体中 Hoxd 基因表达的顺式调控元件存在于鱼类中。我们利用种间转基因方法,发现了颌脊椎动物 Hoxd 增强子之间的功能保守性,证明了来自四足动物、斑马鱼和鳐鱼的同源序列可以在小鼠肢体和斑马鱼鳍中驱动报告基因的表达。我们的研究结果支持了这样一种观点,即与四足动物肢体相关的一些新特征是通过对颌脊椎动物 Hox 调控的顺式和反式作用机制的深度保守修饰而产生的。

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本文引用的文献

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Wiley Interdiscip Rev Syst Biol Med. 2010 Jul-Aug;2(4):422-437. doi: 10.1002/wsbm.70.
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