Ben-Shlomo Izhar, Hsueh Aaron J W
Stanford University School of Medicine, Department of Obstetrics and Gynecology, Division of Reproductive Biology, 300 Pasteur Drive, Room A-344, Stanford, CA 94305-5317, USA.
Mol Endocrinol. 2005 May;19(5):1097-109. doi: 10.1210/me.2004-0451. Epub 2005 Feb 3.
Intercellular communication relies on signal transduction mediated by extracellular ligands and their receptors. Although the ligand-receptor interaction is usually a two-player event, there are selective examples of one polypeptide ligand interacting with more than one phylogenetically unrelated receptor. Likewise, a few receptors interact with more than one polypeptide ligand, and sometimes with more than one coreceptor, likely through an interlocking of unique protein domains. Phylogenetic analyses suggest that for certain triumvirates, the matching events could have taken place at different evolutionary times. In contrast to a few polypeptide ligands interacting with more than one receptor, we found that many small nonpeptide ligands have been paired with two or more plasma membrane receptors, nuclear receptors, or channels. The observation that many small ligands are paired with more than one receptor type highlights the utilitarian use of a limited number of cellular components during metazoan evolution. These conserved ligands are ubiquitous cell metabolites likely favored by natural selection to establish novel regulatory networks. They likely possess structural features useful for designing agonistic and antagonistic drugs to target diverse receptors.
细胞间通讯依赖于由细胞外配体及其受体介导的信号转导。虽然配体 - 受体相互作用通常是两者之间的事件,但存在一些选择性例子,即一种多肽配体与一种以上在系统发育上不相关的受体相互作用。同样,一些受体与一种以上的多肽配体相互作用,有时还与一种以上的共受体相互作用,这可能是通过独特蛋白质结构域的相互连锁实现的。系统发育分析表明,对于某些三联体,匹配事件可能发生在不同的进化时期。与一些多肽配体与一种以上受体相互作用不同,我们发现许多小的非肽配体已与两种或更多种质膜受体、核受体或通道配对。许多小配体与一种以上受体类型配对的观察结果突出了后生动物进化过程中对有限数量细胞成分的功利性利用。这些保守的配体是普遍存在的细胞代谢物,很可能受到自然选择的青睐以建立新的调控网络。它们可能具有有助于设计针对不同受体的激动剂和拮抗剂药物的结构特征。