过度参数化是剖面混合模型的一个问题吗?

IF 6.1 1区 生物学 Q1 EVOLUTIONARY BIOLOGY Systematic Biology Pub Date : 2024-05-27 DOI:10.1093/sysbio/syad063
Hector Baños, Edward Susko, Andrew J Roger
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引用次数: 0

摘要

蛋白质中特定位点上可接受氨基酸的生化限制导致比对位点上氨基酸取代过程的异质性。众所周知,不考虑位点异质性的蛋白质序列进化的系统发育模型容易产生长分支吸引(LBA)假象。开发了轮廓混合物模型,通过位点类别的有限分布来模拟位点处优选氨基酸的异质性,每个位点类别具有一组不同的平衡氨基酸频率。然而,由于过度参数化,这种模型中与许多氨基酸频率向量相关的大量参数是否会对树拓扑估计产生不利影响,这是未知的。在这里,我们从理论上证明,对于长序列,过度参数化不会给轮廓混合模型的估计带来问题。在温和的条件下,树、氨基酸频率和其他模型参数随着序列长度的增加而收敛为真值,即使在频率分布中存在大量分量的情况下也是如此。由于大样本理论并不一定意味着短比对的良好行为,我们探索了这些模型的性能,这些模型使用容易出现LBA伪影的树拓扑模拟短比对。我们发现,对于复杂的剖面混合模型,即使存在许多氨基酸频率向量,过度参数化也不是问题。事实上,站点类很少的简单模型表现不佳。有趣的是,我们还发现,只要位点处氨基酸频率的估计累积分布函数充分接近真实分布函数,氨基酸频率载体的错误指定就不会导致LBA伪影增加。相反,氨基酸交换率的错误指定会严重影响参数估计。最后,我们探讨了在剖面混合物模型中包含一个额外的“F类”的影响,该类表示数据集中氨基酸的总体频率。令人惊讶的是,F类对参数估计没有显著帮助,并且可以降低正确树估计的概率,这取决于场景,尽管它倾向于提高似然性得分。
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Is Over-parameterization a Problem for Profile Mixture Models?

Biochemical constraints on the admissible amino acids at specific sites in proteins lead to heterogeneity of the amino acid substitution process over sites in alignments. It is well known that phylogenetic models of protein sequence evolution that do not account for site heterogeneity are prone to long-branch attraction (LBA) artifacts. Profile mixture models were developed to model heterogeneity of preferred amino acids at sites via a finite distribution of site classes each with a distinct set of equilibrium amino acid frequencies. However, it is unknown whether the large number of parameters in such models associated with the many amino acid frequency vectors can adversely affect tree topology estimates because of over-parameterization. Here, we demonstrate theoretically that for long sequences, over-parameterization does not create problems for estimation with profile mixture models. Under mild conditions, tree, amino acid frequencies, and other model parameters converge to true values as sequence length increases, even when there are large numbers of components in the frequency profile distributions. Because large sample theory does not necessarily imply good behavior for shorter alignments we explore the performance of these models with short alignments simulated with tree topologies that are prone to LBA artifacts. We find that over-parameterization is not a problem for complex profile mixture models even when there are many amino acid frequency vectors. In fact, simple models with few site classes behave poorly. Interestingly, we also found that misspecification of the amino acid frequency vectors does not lead to increased LBA artifacts as long as the estimated cumulative distribution function of the amino acid frequencies at sites adequately approximates the true one. In contrast, misspecification of the amino acid exchangeability rates can severely negatively affect parameter estimation. Finally, we explore the effects of including in the profile mixture model an additional "F-class" representing the overall frequencies of amino acids in the data set. Surprisingly, the F-class does not help parameter estimation significantly and can decrease the probability of correct tree estimation, depending on the scenario, even though it tends to improve likelihood scores.

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来源期刊
Systematic Biology
Systematic Biology 生物-进化生物学
CiteScore
13.00
自引率
7.70%
发文量
70
审稿时长
6-12 weeks
期刊介绍: Systematic Biology is the bimonthly journal of the Society of Systematic Biologists. Papers for the journal are original contributions to the theory, principles, and methods of systematics as well as phylogeny, evolution, morphology, biogeography, paleontology, genetics, and the classification of all living things. A Points of View section offers a forum for discussion, while book reviews and announcements of general interest are also featured.
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