Ravi Vydianathan, Lam Kevin, Tay Boon-Hui, Tay Alice, Brenner Sydney, Venkatesh Byrappa
Institute of Molecular and Cell Biology, ASTAR, Biopolis, Singapore 138673.
Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16327-32. doi: 10.1073/pnas.0907914106. Epub 2009 Sep 3.
We have sequenced and analyzed Hox gene clusters from elephant shark, a holocephalian cartilaginous fish. Elephant shark possesses 4 Hox clusters with 45 Hox genes that include orthologs for a higher number of ancient gnathostome Hox genes than the 4 clusters in tetrapods and the supernumerary clusters in teleost fishes. Phylogenetic analysis of elephant shark Hox genes from 7 paralogous groups that contain all of the 4 members indicated an ((AB)(CD)) topology for the order of Hox cluster duplication, providing support for the 2R hypothesis (i.e., 2 rounds of whole-genome duplication during the early evolution of vertebrates). Comparisons of noncoding sequences of the elephant shark and human Hox clusters have identified a large number of conserved noncoding elements (CNEs), which represent putative cis-regulatory elements that may be involved in the regulation of Hox genes. Interestingly, in fugu more than 50% of these ancient CNEs have diverged beyond recognition in the duplicated (HoxA, HoxB, and HoxD) as well as the singleton (HoxC) Hox clusters. Furthermore, the b-paralogs of the duplicated fugu Hox clusters are virtually devoid of unique ancient CNEs. In contrast to fugu Hox clusters, elephant shark and human Hox clusters have lost fewer ancient CNEs. If these ancient CNEs are indeed enhancers directing tissue-specific expression of Hox genes, divergence of their sequences in vertebrate lineages might have led to altered expression patterns and presumably the functions of their associated Hox genes.
我们对全头亚纲软骨鱼象鲨的Hox基因簇进行了测序和分析。象鲨拥有4个Hox基因簇,共45个Hox基因,其中包含的古代有颌类Hox基因直系同源物数量比四足动物的4个基因簇和硬骨鱼中的额外基因簇更多。对象鲨来自7个旁系同源组的Hox基因进行系统发育分析,这些旁系同源组包含了所有4个成员,结果表明Hox基因簇复制顺序呈((AB)(CD))拓扑结构,为2R假说(即脊椎动物早期进化过程中发生了两轮全基因组复制)提供了支持。对象鲨和人类Hox基因簇的非编码序列进行比较,发现了大量保守非编码元件(CNE),这些元件代表了可能参与Hox基因调控的假定顺式调控元件。有趣的是,在河豚中,超过50%的这些古老CNE在重复的(HoxA、HoxB和HoxD)以及单个的(HoxC)Hox基因簇中已经分化到无法识别。此外,河豚重复的Hox基因簇的b旁系同源物几乎没有独特的古老CNE。与河豚Hox基因簇不同,象鲨和人类Hox基因簇丢失的古老CNE较少。如果这些古老的CNE确实是指导Hox基因组织特异性表达的增强子,那么它们在脊椎动物谱系中的序列分化可能导致表达模式改变,进而可能影响其相关Hox基因的功能。