Li Yuan, Canbäck Björn, Johansson Tomas, Tunlid Anders, Prentice Honor C
Department of Biology, Lund University, Lund, Sweden.
PLoS One. 2015 May 6;10(5):e0125831. doi: 10.1371/journal.pone.0125831. eCollection 2015.
The dimeric metabolic enzyme phosphoglucose isomerase (PGI, EC 5.3.1.9) plays an essential role in energy production. In the grass Festuca ovina, field surveys of enzyme variation suggest that genetic variation at cytosolic PGI (PGIC) may be adaptively important. In the present study, we investigated the molecular basis of the potential adaptive significance of PGIC in F. ovina by analyzing cDNA sequence variation within the PgiC1 gene. Two, complementary, types of selection test both identified PGIC1 codon (amino acid) sites 200 and 173 as candidate targets of positive selection. Both candidate sites involve charge-changing amino acid polymorphisms. On the homology-modeled F. ovina PGIC1 3-D protein structure, the two candidate sites are located on the edge of either the inter-monomer boundary or the inter-domain cleft; examination of the homology-modeled PGIC1 structure suggests that the amino acid changes at the two candidate sites are likely to influence the inter-monomer interaction or the domain-domain packing. Biochemical studies in humans have shown that mutations at several amino acid sites that are located close to the candidate sites in F. ovina, at the inter-monomer boundary or the inter-domain cleft, can significantly change the stability and/or kinetic properties of the PGI enzyme. Molecular evolutionary studies in a wide range of other organisms suggest that PGI amino acid sites with similar locations to those of the candidate sites in F. ovina may be the targets of positive/balancing selection. Candidate sites 200 and 173 are the only sites that appear to discriminate between the two most common PGIC enzyme electromorphs in F. ovina: earlier studies suggest that these electromorphs are implicated in local adaptation to different grassland microhabitats. Our results suggest that PGIC1 sites 200 and 173 are under positive selection in F. ovina.
二聚体代谢酶磷酸葡萄糖异构酶(PGI,EC 5.3.1.9)在能量产生过程中发挥着至关重要的作用。在羊茅属植物羊茅中,对酶变异的田间调查表明,胞质PGI(PGIC)的遗传变异可能具有适应性重要意义。在本研究中,我们通过分析PgiC1基因内的cDNA序列变异,研究了PGIC在羊茅中潜在适应性意义的分子基础。两种互补的选择测试均确定PGIC1密码子(氨基酸)位点200和173为正选择的候选靶点。这两个候选位点均涉及氨基酸电荷变化多态性。在同源建模的羊茅PGIC1三维蛋白质结构上,这两个候选位点位于单体间边界或结构域间裂隙的边缘;对同源建模的PGIC1结构的研究表明,这两个候选位点的氨基酸变化可能会影响单体间相互作用或结构域-结构域堆积。在人类中的生化研究表明,在羊茅中靠近候选位点的几个氨基酸位点发生突变,即在单体间边界或结构域间裂隙处,可显著改变PGI酶的稳定性和/或动力学特性。在其他多种生物中的分子进化研究表明,与羊茅中候选位点位置相似的PGI氨基酸位点可能是正选择/平衡选择的靶点。候选位点200和173是唯一似乎能区分羊茅中两种最常见PGIC酶电泳变体的位点:早期研究表明,这些电泳变体与当地对不同草地微生境的适应性有关。我们的结果表明,PGIC1位点200和173在羊茅中受到正选择。