Whole genome sequencing of mouse lines divergently selected for fatness (FLI) and leanness (FHI) revealed several genetic variants as candidates for novel obesity genes.

IF 1.7 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Genes & genomics Pub Date : 2024-05-01 Epub Date: 2024-03-14 DOI:10.1007/s13258-024-01507-9
Martin Šimon, Špela Mikec, Santosh S Atanur, Janez Konc, Nicholas M Morton, Simon Horvat, Tanja Kunej
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Abstract

Background: Analysing genomes of animal model organisms is widely used for understanding the genetic basis of complex traits and diseases, such as obesity, for which only a few mouse models exist, however, without their lean counterparts.

Objective: To analyse genetic differences in the unique mouse models of polygenic obesity (Fat line) and leanness (Lean line) originating from the same base population and established by divergent selection over more than 60 generations.

Methods: Genetic variability was analysed using WGS. Variants were identified with GATK and annotated with Ensembl VEP. g.Profiler, WebGestalt, and KEGG were used for GO and pathway enrichment analysis. miRNA seed regions were obtained with miRPathDB 2.0, LncRRIsearch was used to predict targets of identified lncRNAs, and genes influencing adipose tissue amount were searched using the IMPC database.

Results: WGS analysis revealed 6.3 million SNPs, 1.3 million were new. Thousands of potentially impactful SNPs were identified, including within 24 genes related to adipose tissue amount. SNP density was highest in pseudogenes and regulatory RNAs. The Lean line carries SNP rs248726381 in the seed region of mmu-miR-3086-3p, which may affect fatty acid metabolism. KEGG analysis showed deleterious missense variants in immune response and diabetes genes, with food perception pathways being most enriched. Gene prioritisation considering SNP GERP scores, variant consequences, and allele comparison with other mouse lines identified seven novel obesity candidate genes: 4930441H08Rik, Aff3, Fam237b, Gm36633, Pced1a, Tecrl, and Zfp536.

Conclusion: WGS revealed many genetic differences between the lines that accumulated over the selection period, including variants with potential negative impacts on gene function. Given the increasing availability of mouse strains and genetic polymorphism catalogues, the study is a valuable resource for researchers to study obesity.

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对因肥胖(FLI)和瘦弱(FHI)而不同的小鼠品系进行的全基因组测序发现了几个候选新型肥胖基因的遗传变异。
背景:分析动物模型生物的基因组被广泛用于了解复杂性状和疾病(如肥胖症)的遗传基础:目的:分析小鼠多基因肥胖(肥胖系)和瘦弱(瘦弱系)模型的遗传差异:方法:使用 WGS 分析遗传变异。使用 miRPathDB 2.0 获取 miRNA 种子区,使用 LncRRIsearch 预测已识别的 lncRNA 的靶标,并使用 IMPC 数据库搜索影响脂肪组织量的基因:WGS分析发现了630万个SNPs,其中130万个是新发现的。结果:WGS分析发现了630万个SNPs,其中130万个是新发现的。发现了数千个具有潜在影响的SNPs,包括24个与脂肪组织数量相关的基因。假基因和调控 RNA 中的 SNP 密度最高。精益系携带的SNP rs248726381位于mmu-miR-3086-3p的种子区,可能会影响脂肪酸代谢。KEGG 分析显示,免疫反应和糖尿病基因中存在有害的错义变异,其中食物感知通路最为丰富。考虑到 SNP GERP 评分、变异后果以及与其他小鼠品系等位基因的比较,基因优先排序确定了七个新的肥胖候选基因:4930441H08Rik、Aff3、Fam237b、Gm36633、Pced1a、Tecrl 和 Zfp536:WGS揭示了小鼠品系之间在选择期间积累的许多遗传差异,包括可能对基因功能产生负面影响的变异。鉴于小鼠品系和遗传多态性目录的可用性越来越高,这项研究是研究人员研究肥胖症的宝贵资源。
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来源期刊
Genes & genomics
Genes & genomics 生物-生化与分子生物学
CiteScore
3.70
自引率
4.80%
发文量
131
审稿时长
6-12 weeks
期刊介绍: Genes & Genomics is an official journal of the Korean Genetics Society (http://kgenetics.or.kr/). Although it is an official publication of the Genetics Society of Korea, membership of the Society is not required for contributors. It is a peer-reviewed international journal publishing print (ISSN 1976-9571) and online version (E-ISSN 2092-9293). It covers all disciplines of genetics and genomics from prokaryotes to eukaryotes from fundamental heredity to molecular aspects. The articles can be reviews, research articles, and short communications.
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