School of Life Sciences, Arizona State University.
Center for Mechanisms of Evolution, Arizona State University.
Genome Biol Evol. 2020 Feb 1;12(2):3917-3925. doi: 10.1093/gbe/evaa016.
Toll-like receptors (TLRs) are a complex family of innate immune genes that are well characterized in mammals and birds but less well understood in nonavian sauropsids (reptiles). The advent of highly contiguous draft genomes of nonmodel organisms enables study of such gene families through analysis of synteny and sequence identity. Here, we analyze TLR genes from the genomes of 22 tetrapod species. Findings reveal a TLR8 gene expansion in crocodilians and turtles (TLR8B), and a second duplication (TLR8C) specifically within turtles, followed by pseudogenization of that gene in the nonfreshwater species (desert tortoise and green sea turtle). Additionally, the Mojave desert tortoise (Gopherus agassizii) has a stop codon in TLR8B (TLR8-1) that is polymorphic among conspecifics. Revised orthology further reveals a new TLR homolog, TLR21-like, which is exclusive to lizards, snakes, turtles, and crocodilians. These analyses were made possible by a new draft genome assembly of the desert tortoise (gopAga2.0), which used chromatin-based assembly to yield draft chromosomal scaffolds (L50 = 26 scaffolds, N50 = 28.36 Mb, longest scaffold = 107 Mb) and an enhanced de novo genome annotation with 25,469 genes. Our three-step approach to orthology curation and comparative analysis of TLR genes shows what new insights are possible using genome assemblies with chromosome-scale scaffolds that permit integration of synteny conservation data.
Toll 样受体 (TLRs) 是一组复杂的先天免疫基因家族,在哺乳动物和鸟类中已有很好的描述,但在非鸟类的蜥形类动物(爬行动物)中了解较少。非模式生物的高度连续草图基因组的出现,使通过分析同线性和序列同一性来研究此类基因家族成为可能。在这里,我们分析了 22 种四足动物物种的 TLR 基因。研究结果表明,鳄鱼和海龟中存在 TLR8 基因扩展(TLR8B),并且在海龟中存在第二个重复(TLR8C),随后该基因在非淡水物种(沙漠龟和绿海龟)中发生了假基因化。此外,莫哈韦沙漠龟(Gopherus agassizii)在 TLR8B(TLR8-1)中存在一个终止密码子,该密码子在同种异体中存在多态性。经过修正的直系同源性进一步揭示了一个新的 TLR 同源物,TLR21 样,它仅存在于蜥蜴、蛇、海龟和鳄鱼中。这些分析是通过对沙漠龟(gopAga2.0)的新草案基因组组装实现的,该组装使用基于染色质的组装方法生成了草案染色体支架(L50 = 26 个支架,N50 = 28.36 Mb,最长支架 = 107 Mb),并通过 25469 个基因增强了从头基因组注释。我们的三步骤同源性校正方法和 TLR 基因的比较分析表明,使用具有染色体规模支架的基因组组装可以实现什么样的新见解,这些支架允许整合同线性保守数据。