Tucker R P, Drabikowski K, Hess J F, Ferralli J, Chiquet-Ehrismann R, Adams J C
Department of Cell Biology and Human Anatomy, University of California at Davis, Davis, CA 95616, USA.
BMC Evol Biol. 2006 Aug 7;6:60. doi: 10.1186/1471-2148-6-60.
Tenascins are a family of glycoproteins found primarily in the extracellular matrix of embryos where they help to regulate cell proliferation, adhesion and migration. In order to learn more about their origins and relationships to each other, as well as to clarify the nomenclature used to describe them, the tenascin genes of the urochordate Ciona intestinalis, the pufferfish Tetraodon nigroviridis and Takifugu rubripes and the frog Xenopus tropicalis were identified and their gene organization and predicted protein products compared with the previously characterized tenascins of amniotes.
A single tenascin gene was identified in the genome of C. intestinalis that encodes a polypeptide with domain features common to all vertebrate tenascins. Both pufferfish genomes encode five tenascin genes: two tenascin-C paralogs, a tenascin-R with domain organization identical to mammalian and avian tenascin-R, a small tenascin-X with previously undescribed GK repeats, and a tenascin-W. Four tenascin genes corresponding to tenascin-C, tenascin-R, tenascin-X and tenascin-W were also identified in the X. tropicalis genome. Multiple sequence alignment reveals that differences in the size of tenascin-W from various vertebrate classes can be explained by duplications of specific fibronectin type III domains. The duplicated domains are encoded on single exons and contain putative integrin-binding motifs. A phylogenetic tree based on the predicted amino acid sequences of the fibrinogen-related domains demonstrates that tenascin-C and tenascin-R are the most closely related vertebrate tenascins, with the most conserved repeat and domain organization. Taking all lines of evidence together, the data show that the tenascins referred to as tenascin-Y and tenascin-N are actually members of the tenascin-X and tenascin-W gene families, respectively.
The presence of a tenascin gene in urochordates but not other invertebrate phyla suggests that tenascins may be specific to chordates. Later genomic duplication events led to the appearance of four family members in vertebrates: tenascin-C, tenascin-R, tenascin-W and tenascin-X.
腱糖蛋白是一类主要存在于胚胎细胞外基质中的糖蛋白,它们有助于调节细胞增殖、黏附和迁移。为了更深入了解它们的起源、相互关系,以及厘清用于描述它们的命名法,对尾索动物玻璃海鞘、河豚黑青斑河鲀和红鳍东方鲀以及青蛙热带爪蟾的腱糖蛋白基因进行了鉴定,并将它们的基因结构和预测的蛋白质产物与先前已鉴定的羊膜动物腱糖蛋白进行了比较。
在玻璃海鞘的基因组中鉴定出一个单一的腱糖蛋白基因,该基因编码一种具有所有脊椎动物腱糖蛋白共同结构域特征的多肽。两种河豚基因组都编码五个腱糖蛋白基因:两个腱糖蛋白-C旁系同源物、一个结构域组织与哺乳动物和鸟类腱糖蛋白-R相同的腱糖蛋白-R、一个具有先前未描述的GK重复序列的小型腱糖蛋白-X,以及一个腱糖蛋白-W。在热带爪蟾的基因组中也鉴定出了与腱糖蛋白-C、腱糖蛋白-R、腱糖蛋白-X和腱糖蛋白-W相对应的四个腱糖蛋白基因。多序列比对显示,不同脊椎动物类群的腱糖蛋白-W大小差异可由特定纤连蛋白III型结构域的重复来解释。重复的结构域由单个外显子编码,并包含假定的整合素结合基序。基于纤维蛋白原相关结构域预测氨基酸序列构建的系统发育树表明,腱糖蛋白-C和腱糖蛋白-R是脊椎动物中关系最密切的腱糖蛋白,具有最保守的重复序列和结构域组织。综合所有证据来看,数据表明被称为腱糖蛋白-Y和腱糖蛋白-N的腱糖蛋白实际上分别是腱糖蛋白-X和腱糖蛋白-W基因家族的成员。
尾索动物中存在腱糖蛋白基因,而其他无脊椎动物门中不存在,这表明腱糖蛋白可能是脊索动物特有的。后来的基因组重复事件导致脊椎动物中出现了四个家族成员:腱糖蛋白-C、腱糖蛋白-R、腱糖蛋白-W和腱糖蛋白-X。