Wilkins J F, Haig D
Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, USA.
Proc Biol Sci. 2001 Sep 22;268(1479):1861-7. doi: 10.1098/rspb.2001.1651.
We present a model that considers the coevolution of genomic imprinting at a growth factor locus and an antagonistic growth suppressor locus. With respect to the two loci considered independently, our model makes the familiar predictions that an imprinted growth factor locus will only be expressed from the paternally derived allele and an imprinted growth suppressor locus only from the maternally derived allele. In addition, our coevolutionary model allows us to make predictions regarding the sequence of evolutionary events necessary for generating such a system. We conclude that imprinting at the growth factor locus preceded the evolution of growth suppressor function at the second locus, which in turn preceded imprinting at that locus. We then discuss the consistency of these predictions with currently available comparative data on the insulin-like growth factor 2 insulin-like growth factor 2 receptor system of mammals.
我们提出了一个模型,该模型考虑了生长因子基因座和拮抗性生长抑制基因座上基因组印记的共同进化。就独立考虑的这两个基因座而言,我们的模型得出了常见的预测结果:印记生长因子基因座仅从父本来源的等位基因表达,而印记生长抑制基因座仅从母本来源的等位基因表达。此外,我们的共同进化模型使我们能够对产生这样一个系统所需的进化事件序列进行预测。我们得出结论,生长因子基因座上的印记先于第二个基因座上生长抑制功能的进化,而这又先于该基因座上的印记。然后,我们讨论了这些预测与目前关于哺乳动物胰岛素样生长因子2 - 胰岛素样生长因子2受体系统的比较数据的一致性。