Department of Natural History, Royal Ontario Museum, Toronto, Ontario, Canada.
Department of Ecology and Evolutionary Biology, University of Toronto, Ontario, Canada.
Genome Biol Evol. 2021 Jan 7;13(1). doi: 10.1093/gbe/evaa242.
Bloodfeeding is employed by many parasitic animals and requires specific innovations for efficient feeding. Some of these innovations are molecular features that are related to the inhibition of hemostasis. For example, bloodfeeding insects, bats, and leeches release proteins with anticoagulatory activity through their salivary secretions. The antistasin-like protein family, composed of serine protease inhibitors with one or more antistasin-like domains, is tightly linked to inhibition of hemostasis in leeches. However, this protein family has been recorded also in non-bloodfeeding invertebrates, such as cnidarians, mollusks, polychaetes, and oligochaetes. The present study aims to 1) root the antistasin-like gene tree and delimit the major orthologous groups, 2) identify potential independent origins of salivary proteins secreted by leeches, and 3) identify major changes in domain and/or motif structure within each orthologous group. Five clades containing leech antistasin-like proteins are distinguishable through rigorous phylogenetic analyses based on nine new transcriptomes and a diverse set of comparative data: the trypsin + leukocyte elastase inhibitors clade, the antistasin clade, the therostasin clade, and two additional, unnamed clades. The antistasin-like gene tree supports multiple origins of leech antistasin-like proteins due to the presence of both leech and non-leech sequences in one of the unnamed clades, but a single origin of factor Xa and trypsin + leukocyte elastase inhibitors. This is further supported by three sequence motifs that are exclusive to antistasins, the trypsin + leukocyte elastase inhibitor clade, and the therostasin clade, respectively. We discuss the implications of our findings for the evolution of this diverse family of leech anticoagulants.
吸血是许多寄生虫动物采用的一种方式,需要特定的创新来实现高效的吸血。其中一些创新是与止血抑制相关的分子特征。例如,吸血昆虫、蝙蝠和水蛭通过唾液分泌释放具有抗凝活性的蛋白质。抗凝血酶样蛋白家族由具有一个或多个抗凝血酶样结构域的丝氨酸蛋白酶抑制剂组成,与水蛭的止血抑制密切相关。然而,这个蛋白家族也在非吸血无脊椎动物中被记录下来,如刺胞动物、软体动物、多毛类和寡毛类。本研究旨在:1)构建抗凝血酶样基因树并划定主要的直系同源群;2)识别由水蛭分泌的唾液蛋白的潜在独立起源;3)识别每个直系同源群中结构域和/或基序结构的主要变化。通过基于九个新转录组和多样化的比较数据集的严格系统发育分析,可以区分包含水蛭抗凝血酶样蛋白的五个进化枝:胰蛋白酶+白细胞弹性蛋白酶抑制剂进化枝、抗凝血酶进化枝、therostasin 进化枝和另外两个未命名的进化枝。抗凝血酶样基因树支持水蛭抗凝血酶样蛋白的多个起源,因为在一个未命名的进化枝中存在水蛭和非水蛭序列,但因子 Xa 和胰蛋白酶+白细胞弹性蛋白酶抑制剂只有一个起源。这进一步得到了三个序列基序的支持,这三个基序分别是抗凝血酶所特有的、胰蛋白酶+白细胞弹性蛋白酶抑制剂进化枝所特有的和 therostasin 进化枝所特有的。我们讨论了我们的发现对这个多样化的水蛭抗凝剂家族的进化的影响。