Osorio Daniel S, Antunes Agostinho, Ramos Maria J
REQUIMTE, Departamento de Química, Faculdade de Ciências, Universidade do Porto, Rua do Campo Alegre, 687, 4169-007 Porto, Portugal.
BMC Evol Biol. 2007 Sep 20;7:167. doi: 10.1186/1471-2148-7-167.
Angiogenesis, the formation of new blood vessels, is a primordial process in development and its dysregulation has a central role in the pathogenesis of many diseases. Angiogenin (ANG), a peculiar member of the RNase A superfamily, is a potent inducer of angiogenesis involved in many different types of cancer, amyotrophic lateral sclerosis and also with a possible role in the innate immune defense. The evolutionary path of this family has been a highly dynamic one, where positive selection has played a strong role. In this work we used a combined gene and protein level approach to determine the main sites under diversifying selection on the primate ANG gene and analyze its structural and functional implications.
We obtained evidence for positive selection in the primate ANG gene. Site specific analysis pointed out 15 sites under positive selection, most of which also exhibited drastic changes in amino acid properties. The mapping of these sites in the ANG 3D-structure described five clusters, four of which were located in functional regions: two in the active site region, one in the nucleolar location signal and one in the cell-binding site. Eight of the 15 sites under selection in the primate ANG gene were highly or moderately conserved in the RNase A family, suggesting a directed event and not a simple consequence of local structural or functional permissiveness. Moreover, 11 sites were exposed to the surface of the protein indicating that they may influence the interactions performed by ANG.
Using a maximum likelihood gene level analysis we identified 15 sites under positive selection in the primate ANG genes, that were further corroborated through a protein level analysis of radical changes in amino acid properties. These sites mapped onto the main functional regions of the ANG protein. The fact that evidence for positive selection is present in all ANG regions required for angiogenesis may be a good indication that angiogenesis is the process under selection. However, other possibilities to be considered arise from the possible involvement of ANG in innate immunity and the potential influence or co-evolution with its interacting proteins and ligands.
血管生成,即新血管的形成,是发育过程中的一个原始过程,其失调在许多疾病的发病机制中起着核心作用。血管生成素(ANG)是核糖核酸酶A超家族的一个特殊成员,是血管生成的有效诱导剂,参与许多不同类型的癌症、肌萎缩侧索硬化症,并且在先天免疫防御中可能也发挥作用。该家族的进化路径一直是高度动态的,其中正选择发挥了重要作用。在这项工作中,我们采用基因和蛋白质水平相结合的方法来确定灵长类动物ANG基因在多样化选择下的主要位点,并分析其结构和功能意义。
我们获得了灵长类动物ANG基因存在正选择的证据。位点特异性分析指出了15个处于正选择下的位点,其中大多数位点的氨基酸性质也发生了剧烈变化。这些位点在ANG三维结构上的定位描述了五个簇,其中四个位于功能区域:两个在活性位点区域,一个在核仁定位信号区域,一个在细胞结合位点。灵长类动物ANG基因中15个被选择的位点中有8个在核糖核酸酶A家族中高度或中度保守,这表明这是一个定向事件,而不是局部结构或功能许可的简单结果。此外,11个位点暴露于蛋白质表面,表明它们可能影响ANG进行的相互作用。
通过最大似然基因水平分析,我们在灵长类动物ANG基因中鉴定出15个处于正选择下的位点,通过对氨基酸性质的剧烈变化进行蛋白质水平分析进一步证实了这些位点。这些位点映射到ANG蛋白的主要功能区域。血管生成所需的所有ANG区域都存在正选择的证据,这可能很好地表明血管生成是被选择的过程。然而,由于ANG可能参与先天免疫以及与其相互作用的蛋白质和配体的潜在影响或共同进化,还需要考虑其他可能性。