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多样性远交系(Diversity Outbred)小鼠的面部形状和异速生长数量性状基因座区间富含已知的骨骼和面部发育基因。

Facial shape and allometry quantitative trait locus intervals in the Diversity Outbred mouse are enriched for known skeletal and facial development genes.

机构信息

Department of Cell Biology & Anatomy, Alberta Children's Hospital Research Institute and McCaig Bone and Joint Institute, Cumming School of Medicine, University of Calgary, AB, Canada.

Department of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, United States of America.

出版信息

PLoS One. 2020 Jun 5;15(6):e0233377. doi: 10.1371/journal.pone.0233377. eCollection 2020.

Abstract

The biology of how faces are built and come to differ from one another is complex. Discovering normal variants that contribute to differences in facial morphology is one key to untangling this complexity, with important implications for medicine and evolutionary biology. This study maps quantitative trait loci (QTL) for skeletal facial shape using Diversity Outbred (DO) mice. The DO is a randomly outcrossed population with high heterozygosity that captures the allelic diversity of eight inbred mouse lines from three subspecies. The study uses a sample of 1147 DO animals (the largest sample yet employed for a shape QTL study in mouse), each characterized by 22 three-dimensional landmarks, 56,885 autosomal and X-chromosome markers, and sex and age classifiers. We identified 37 facial shape QTL across 20 shape principal components (PCs) using a mixed effects regression that accounts for kinship among observations. The QTL include some previously identified intervals as well as new regions that expand the list of potential targets for future experimental study. Three QTL characterized shape associations with size (allometry). Median support interval size was 3.5 Mb. Narrowing additional analysis to QTL for the five largest magnitude shape PCs, we found significant overrepresentation of genes with known roles in growth, skeletal and facial development, and sensory organ development. For most intervals, one or more of these genes lies within 0.25 Mb of the QTL's peak. QTL effect sizes were small, with none explaining more than 0.5% of facial shape variation. Thus, our results are consistent with a model of facial diversity that is influenced by key genes in skeletal and facial development and, simultaneously, is highly polygenic.

摘要

面部结构差异的生物学机制非常复杂。发现导致面部形态差异的正常变异是解开这一复杂性的关键之一,这对医学和进化生物学具有重要意义。本研究使用多样性杂交(DO)小鼠来绘制骨骼面部形状的数量性状基因座(QTL)图谱。DO 是一种随机杂交的种群,具有高度的杂合性,可以捕获来自三个亚种的 8 个近交系小鼠的等位基因多样性。该研究使用了 1147 只 DO 动物的样本(这是迄今为止在小鼠形状 QTL 研究中使用的最大样本),每个样本都具有 22 个三维标志、56885 个常染色体和 X 染色体标记以及性别和年龄分类器。我们使用混合效应回归,根据观察值之间的亲缘关系,在 20 个形状主成分(PC)中鉴定出 37 个面部形状 QTL。这些 QTL 包括一些先前确定的区间以及新的区域,扩大了未来实验研究的潜在目标列表。三个 QTL 描述了与大小(生长比)相关的形状关联。中位数支持区间大小为 3.5Mb。将进一步分析缩小到五个最大幅度形状 PC 的 QTL,我们发现具有已知在生长、骨骼和面部发育以及感觉器官发育中作用的基因的显著代表性。对于大多数区间,这些基因中的一个或多个位于 QTL 峰的 0.25Mb 内。QTL 效应大小较小,没有一个解释超过面部形状变异的 0.5%。因此,我们的结果与一个模型一致,即面部多样性受骨骼和面部发育中的关键基因影响,同时高度多基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b05c/7274373/0a5011056670/pone.0233377.g001.jpg

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