Lossow Kristina, Hübner Sandra, Roudnitzky Natacha, Slack Jay P, Pollastro Federica, Behrens Maik, Meyerhof Wolfgang
From the Department of Molecular Genetics, German Institute of Human Nutrition Potsdam-Rehbruecke, Arthur-Scheunert-Allee 114-116, 14558 Nuthetal, Germany.
the Givaudan Flavors Corporation, Cincinnati, Ohio 45216, and.
J Biol Chem. 2016 Jul 15;291(29):15358-77. doi: 10.1074/jbc.M116.718544. Epub 2016 May 20.
One key to animal survival is the detection and avoidance of potentially harmful compounds by their bitter taste. Variable numbers of taste 2 receptor genes expressed in the gustatory end organs enable bony vertebrates (Euteleostomi) to recognize numerous bitter chemicals. It is believed that the receptive ranges of bitter taste receptor repertoires match the profiles of bitter chemicals that the species encounter in their diets. Human and mouse genomes contain pairs of orthologous bitter receptor genes that have been conserved throughout evolution. Moreover, expansions in both lineages generated species-specific sets of bitter taste receptor genes. It is assumed that the orthologous bitter taste receptor genes mediate the recognition of bitter toxins relevant for both species, whereas the lineage-specific receptors enable the detection of substances differently encountered by mice and humans. By challenging 34 mouse bitter taste receptors with 128 prototypical bitter substances in a heterologous expression system, we identified cognate compounds for 21 receptors, 19 of which were previously orphan receptors. We have demonstrated that mouse taste 2 receptors, like their human counterparts, vary greatly in their breadth of tuning, ranging from very broadly to extremely narrowly tuned receptors. However, when compared with humans, mice possess fewer broadly tuned receptors and an elevated number of narrowly tuned receptors, supporting the idea that a large receptor repertoire is the basis for the evolution of specialized receptors. Moreover, we have demonstrated that sequence-orthologous bitter taste receptors have distinct agonist profiles. Species-specific gene expansions have enabled further diversification of bitter substance recognition spectra.
动物生存的一个关键是通过苦味来检测和避免潜在的有害化合物。味觉终末器官中表达的味觉2受体基因数量各异,这使硬骨脊椎动物(真口类)能够识别多种苦味化学物质。据信,苦味受体库的感受范围与物种在饮食中遇到的苦味化学物质的特征相匹配。人类和小鼠基因组包含在整个进化过程中保守的直系同源苦味受体基因对。此外,两个谱系中的基因扩张产生了物种特异性的苦味受体基因集。据推测,直系同源苦味受体基因介导对两种物种都相关的苦味毒素的识别,而谱系特异性受体则使小鼠和人类能够检测到不同遇到的物质。通过在异源表达系统中用128种典型苦味物质挑战34种小鼠苦味受体,我们确定了21种受体的同源化合物,其中19种以前是孤儿受体。我们已经证明,小鼠味觉2受体与其人类对应物一样,其调谐广度差异很大,从非常宽泛调谐的受体到极其狭窄调谐的受体都有。然而,与人类相比,小鼠拥有较少的宽泛调谐受体和较多的狭窄调谐受体,这支持了一个观点,即大量受体库是专门化受体进化的基础。此外,我们已经证明序列直系同源的苦味受体具有不同的激动剂谱。物种特异性基因扩张使苦味物质识别谱进一步多样化。