Wotton Karl R, Weierud Frida K, Dietrich Susanne, Lewis Katharine E
King's College London, Department of Craniofacial Development, Floor 27 Guy's Tower, Guy's Hospital, London Bridge, London, SE1 9RT, UK.
BMC Evol Biol. 2008 Jun 9;8:171. doi: 10.1186/1471-2148-8-171.
Lbx/ladybird genes originated as part of the metazoan cluster of Nk homeobox genes. In all animals investigated so far, both the protostome genes and the vertebrate Lbx1 genes were found to play crucial roles in neural and muscle development. Recently however, additional Lbx genes with divergent expression patterns were discovered in amniotes. Early in the evolution of vertebrates, two rounds of whole genome duplication are thought to have occurred, during which 4 Lbx genes were generated. Which of these genes were maintained in extant vertebrates, and how these genes and their functions evolved, is not known.
Here we searched vertebrate genomes for Lbx genes and discovered novel members of this gene family. We also identified signature genes linked to particular Lbx loci and traced the remnants of 4 Lbx paralogons (two of which retain Lbx genes) in amniotes. In teleosts, that have undergone an additional genome duplication, 8 Lbx paralogons (three of which retain Lbx genes) were found. Phylogenetic analyses of Lbx and Lbx-associated genes show that in extant, bony vertebrates only Lbx1- and Lbx2-type genes are maintained. Of these, some Lbx2 sequences evolved faster and were probably subject to neofunctionalisation, while Lbx1 genes may have retained more features of the ancestral Lbx gene. Genes at Lbx1 and former Lbx4 loci are more closely related, as are genes at Lbx2 and former Lbx3 loci. This suggests that during the second vertebrate genome duplication, Lbx1/4 and Lbx2/3 paralogons were generated from the duplicated Lbx loci created during the first duplication event.
Our study establishes for the first time the evolutionary history of Lbx genes in bony vertebrates, including the order of gene duplication events, gene loss and phylogenetic relationships. Moreover, we identified genetic hallmarks for each of the Lbx paralogons that can be used to trace Lbx genes as other vertebrate genomes become available. Significantly, we show that bony vertebrates only retained copies of Lbx1 and Lbx2 genes, with some Lbx2 genes being highly divergent. Thus, we have established a base on which the evolution of Lbx gene function in vertebrate development can be evaluated.
Lbx/瓢虫基因起源于后生动物Nk同源框基因簇。在迄今为止研究的所有动物中,原口动物基因和脊椎动物Lbx1基因都在神经和肌肉发育中发挥着关键作用。然而,最近在羊膜动物中发现了具有不同表达模式的其他Lbx基因。在脊椎动物进化早期,人们认为发生了两轮全基因组复制,在此期间产生了4个Lbx基因。这些基因中哪些在现存脊椎动物中得以保留,以及这些基因及其功能是如何进化的,目前尚不清楚。
在此,我们在脊椎动物基因组中搜索Lbx基因,并发现了该基因家族的新成员。我们还鉴定了与特定Lbx基因座相关的标志性基因,并追踪了羊膜动物中4个Lbx旁系同源基因簇(其中两个保留Lbx基因)的遗迹。在经历了一次额外基因组复制的硬骨鱼中,发现了8个Lbx旁系同源基因簇(其中三个保留Lbx基因)。对Lbx及与Lbx相关基因的系统发育分析表明,在现存的硬骨脊椎动物中,仅保留了Lbx1型和Lbx2型基因。其中,一些Lbx2序列进化得更快,可能经历了新功能化,而Lbx1基因可能保留了更多祖先Lbx基因的特征。Lbx1和前Lbx4基因座处的基因关系更密切,Lbx2和前Lbx3基因座处的基因也是如此。这表明在第二次脊椎动物基因组复制期间,Lbx1/4和Lbx2/3旁系同源基因簇是由第一次复制事件中产生的复制Lbx基因座形成的。
我们的研究首次确立了硬骨脊椎动物中Lbx基因的进化史,包括基因复制事件的顺序、基因丢失和系统发育关系。此外,我们为每个Lbx旁系同源基因簇鉴定了遗传标记,随着其他脊椎动物基因组的可得,这些标记可用于追踪Lbx基因。重要的是,我们表明硬骨脊椎动物仅保留了Lbx1和Lbx2基因的拷贝,其中一些Lbx2基因高度分化。因此,我们建立了一个基础,据此可以评估脊椎动物发育中Lbx基因功能的进化。