Department of Bioinformatics and Genomics University of North Carolina at Charlotte, 9201 University City Boulevard Charlotte, NC 28223, USA.
Marine LaboratoryUniversity of GuamMangilao, GU 96913, USA; ARC Centre of Excellence for Coral Reef StudiesJames Cook UniversityTownsville, Queensland 4811, Australia.
R Soc Open Sci. 2015 Dec 4;2(12):150377. doi: 10.1098/rsos.150377. eCollection 2015 Dec.
Tissue inhibitors of metalloproteinases (TIMPs) help regulate the extracellular matrix (ECM) in animals, mostly by inhibiting matrix metalloproteinases (MMPs). They are important activators of mutable collagenous tissue (MCT), which have been extensively studied in echinoderms, and the four TIMP copies in humans have been studied for their role in cancer. To understand the evolution of TIMPs, we combined 405 TIMPs from an echinoderm transcriptome dataset built from 41 specimens representing all five classes of echinoderms with variants from protostomes and chordates. We used multiple sequence alignment with various stringencies of alignment quality to cull highly divergent sequences and then conducted phylogenetic analyses using both nucleotide and amino acid sequences. Phylogenetic hypotheses consistently recovered TIMPs as diversifying in the ancestral deuterostome and these early lineages continuing to diversify in echinoderms. The four vertebrate TIMPs diversified from a single copy in the ancestral chordate, all other copies being lost. Consistent with greater MCT needs owing to body wall liquefaction, evisceration, autotomy and reproduction by fission, holothuroids had significantly more TIMPs and higher read depths per contig. Ten cysteine residues, an HPQ binding site and several other residues were conserved in at least 70% of all TIMPs. The conservation of binding sites and the placement of echinoderm TIMPs involved in MCT modification suggest that ECM regulation remains the primary function of TIMP genes, although within this role there are a large number of specialized copies.
组织金属蛋白酶抑制剂(TIMPs)有助于调节动物的细胞外基质(ECM),主要通过抑制基质金属蛋白酶(MMPs)来实现。它们是可变胶原组织(MCT)的重要激活剂,在棘皮动物中得到了广泛研究,人类的 4 种 TIMP 拷贝也因其在癌症中的作用而受到研究。为了了解 TIMPs 的进化,我们结合了来自棘皮动物转录组数据集的 405 种 TIMP,该数据集由代表棘皮动物五个类群的 41 个标本构建,其中包含来自原口动物和脊索动物的变体。我们使用多种序列比对方法,对不同的比对质量进行严格筛选,然后使用核苷酸和氨基酸序列进行系统发育分析。系统发育假说一致表明,TIMP 在祖先后口动物中多样化,这些早期谱系在棘皮动物中继续多样化。四种脊椎动物 TIMP 从祖先脊索动物的单一拷贝中多样化而来,其他拷贝均丢失。由于身体壁的液化、内脏的排出、自切和通过分裂进行繁殖,海参类动物具有更多的 TIMP 和更高的每个 contig 的读深,这与它们对 MCT 的需求更大有关。至少有 70%的所有 TIMP 都保守着 10 个半胱氨酸残基、一个 HPQ 结合位点和其他几个残基。结合位点的保守性和参与 MCT 修饰的棘皮动物 TIMP 的位置表明,ECM 调节仍然是 TIMP 基因的主要功能,尽管在这个角色中存在大量专门的拷贝。