Bahudhanapati Harinath, Bhattacharya Shashwati, Wei Shuo
Department of Biology, West Virginia University, Morgantown, WV, United States of America.
PLoS One. 2015 Aug 26;10(8):e0136281. doi: 10.1371/journal.pone.0136281. eCollection 2015.
Members of the disintegrin metalloproteinase (ADAM) family have important functions in regulating cell-cell and cell-matrix interactions as well as cell signaling. There are two major types of ADAMs: the somatic ADAMs (sADAMs) that have a significant presence in somatic tissues, and the testicular ADAMs (tADAMs) that are expressed predominantly in the testis. Genes encoding tADAMs can be further divided into two groups: group I (intronless) and group II (intron-containing). To date, tAdams have only been reported in placental mammals, and their evolutionary origin and relationship to sAdams remain largely unknown. Using phylogenetic and syntenic tools, we analyzed the Adam genes in various vertebrates ranging from fishes to placental mammals. Our analyses reveal duplication and loss of some sAdams in certain vertebrate species. In particular, there exists an Adam9-like gene in non-mammalian vertebrates but not mammals. We also identified putative group I and group II tAdams in all amniote species that have been examined. These tAdam homologues are more closely related to Adams 9 and 9-like than to other sAdams. In all amniote species examined, group II tAdams lie in close vicinity to Adam9 and hence likely arose from tandem duplication, whereas group I tAdams likely originated through retroposition because of their lack of introns. Clusters of multiple group I tAdams are also common, suggesting tandem duplication after retroposition. Therefore, Adam9/9-like and some of the derived tAdam loci are likely preferred targets for tandem duplication and/or retroposition. Consistent with this hypothesis, we identified a young retroposed gene that duplicated recently from Adam9 in the opossum. As a result of gene duplication, some tAdams were pseudogenized in certain species, whereas others acquired new expression patterns and functions. The rapid duplication of Adam genes has a major contribution to the diversity of ADAMs in various vertebrate species.
解整合素金属蛋白酶(ADAM)家族成员在调节细胞-细胞和细胞-基质相互作用以及细胞信号传导方面具有重要功能。ADAM主要有两种类型:在体细胞组织中大量存在的体细胞ADAM(sADAM),以及主要在睾丸中表达的睾丸ADAM(tADAM)。编码tADAM的基因可进一步分为两组:第一组(无内含子)和第二组(含内含子)。迄今为止,tADAM仅在胎盘哺乳动物中被报道,它们的进化起源以及与sADAM的关系在很大程度上仍然未知。我们使用系统发育和共线性工具,分析了从鱼类到胎盘哺乳动物等各种脊椎动物中的Adam基因。我们的分析揭示了某些脊椎动物物种中一些sADAM的重复和丢失。特别是,在非哺乳动物脊椎动物中存在一个类似Adam9的基因,但在哺乳动物中不存在。我们还在所有已检测的羊膜动物物种中鉴定出了推定的第一组和第二组tADAM。这些tADAM同源物与Adam9和类似Adam9的基因的关系比与其他sADAM的关系更密切。在所有检测的羊膜动物物种中,第二组tADAM与Adam9紧密相邻,因此可能起源于串联重复,而第一组tADAM可能由于缺乏内含子而起源于反转录转座。多个第一组tADAM的簇也很常见,这表明反转录转座后发生了串联重复。因此,Adam9/类似Adam9的基因以及一些衍生的tADAM基因座可能是串联重复和/或反转录转座的首选靶点。与这一假设一致,我们在负鼠中鉴定出了一个最近从Adam9复制而来的年轻反转录基因。由于基因重复,一些tADAM在某些物种中被假基因化,而另一些则获得了新的表达模式和功能。Adam基因的快速重复对各种脊椎动物物种中ADAM的多样性有重大贡献。