Parnell Nicholas F, Hulsey C Darrin, Streelman J Todd
School of Biology, Institute for Bioengineering and Bioscience, Georgia Institute of Technology, 310 Ferst Drive, Atlanta, GA 30332-0230, USA.
BMC Evol Biol. 2008 Apr 28;8:122. doi: 10.1186/1471-2148-8-122.
Evolutionary biologists want to explain the origin of novel features and functions. Two recent but separate lines of research address this question. The first describes one possible outcome of hybridization, called transgressive segregation, where hybrid offspring exhibit trait distributions outside of the parental range. The second considers the explicit mapping of form to function and illustrates manifold paths to similar function (called many to one mapping, MTOM) when the relationship between the two is complex. Under this scenario, functional novelty may be a product of the number of ways to elicit a functional outcome (i.e., the degree of MTOM). We fuse these research themes by considering the influence of MTOM on the production of transgressive jaw biomechanics in simulated hybrids between Lake Malawi cichlid species.
We characterized the component links and functional output (kinematic transmission, KT) of the 4-bar mechanism in the oral jaws of Lake Malawi cichlids. We demonstrated that the input and output links, the length of the lower jaw and the length of the maxilla respectively, have consistent but opposing relationships with KT. Based on these data, we predicted scenarios in which species with different morphologies but similar KT (MTOM species) would produce transgressive function in hybrids. We used a simple but realistic genetic model to show that transgressive function is a likely outcome of hybridization among Malawi species exhibiting MTOM. Notably, F2 hybrids are transgressive for function (KT), but not the component links that contribute to function. In our model, transgression is a consequence of recombination and assortment among alleles specifying the lengths of the lower jaw and maxilla.
We have described a general and likely pervasive mechanism that generates functional novelty. Simulations of hybrid offspring among Lake Malawi cichlids exhibiting MTOM produce transgressive function in the majority of cases, and at appreciable frequency. Functional transgression (i) is a product of recombination and assortment between alleles controlling the lengths of the lower jaw and the maxilla, (ii) occurs in the absence of transgressive morphology, and (iii) can be predicted from the morphology of parents. Our genetic model can be tested by breeding Malawi cichlid hybrids in the laboratory and examining the resulting range of forms and functions.
进化生物学家想要解释新特征和新功能的起源。最近有两条独立的研究路线探讨了这个问题。第一条描述了杂交的一种可能结果,称为超亲分离,即杂交后代表现出超出亲本范围的性状分布。第二条考虑了形态到功能的明确映射,并说明了当两者之间的关系复杂时,通向相似功能的多种途径(称为多对一映射,MTOM)。在这种情况下,功能新奇可能是引发功能结果的方式数量(即MTOM程度)的产物。我们通过考虑MTOM对马拉维湖丽鱼科物种模拟杂交中产生超亲颌骨生物力学的影响,将这些研究主题融合在一起。
我们表征了马拉维湖丽鱼科鱼类口腔颌骨中四杆机构的组成环节和功能输出(运动传递,KT)。我们证明输入和输出环节,即下颌长度和上颌长度,分别与KT具有一致但相反的关系。基于这些数据,我们预测了具有不同形态但相似KT的物种(MTOM物种)在杂交中会产生超亲功能的情况。我们使用了一个简单但现实的遗传模型来表明,超亲功能是表现出MTOM的马拉维物种杂交的可能结果。值得注意的是,F2代杂种在功能(KT)上是超亲的,但对促成功能的组成环节则不然。在我们的模型中,超亲是指定下颌和上颌长度的等位基因之间重组和分离的结果。
我们描述了一种产生功能新奇的普遍且可能广泛存在的机制。对表现出MTOM的马拉维湖丽鱼科杂交后代的模拟在大多数情况下会以可观的频率产生超亲功能。功能超亲(i)是控制下颌和上颌长度的等位基因之间重组和分离的产物,(ii)在没有超亲形态的情况下发生,并且(iii)可以从亲本的形态预测。我们的遗传模型可以通过在实验室中培育马拉维湖丽鱼科杂种并检查由此产生的形态和功能范围来进行测试。