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里昂高血压同源基因大鼠的身体成分和代谢变化以及作为定位候选基因的鉴定。

Body Composition and Metabolic Changes in a Lyon Hypertensive Congenic Rat and Identification of as a Positional Candidate Gene.

作者信息

Clark Karen C, Wagner Valerie A, Holl Katie L, Reho John J, Tutaj Monika, Smith Jennifer R, Dwinell Melinda R, Grobe Justin L, Kwitek Anne E

机构信息

Department of Physiology, Medical College of Wisconsin, Milwaukee, WI, United States.

Comprehensive Rodent Metabolic Phenotyping Core, Medical College of Wisconsin, Milwaukee, WI, United States.

出版信息

Front Genet. 2022 Jun 24;13:903971. doi: 10.3389/fgene.2022.903971. eCollection 2022.

Abstract

Central obesity is genetically complex, and its exponential increase in the last decades have made it a critical public health issue. The Lyon Hypertensive (LH) rat is a well-characterized hypertensive model that also exhibits spontaneous and profound differences in body weight and adiposity, relative to its metabolically healthy control, the Lyon Normotensive (LN) rat. The mechanisms underlying the body weight differences between these strains are not well-understood, thus a congenic model (LHLNa) was developed where a portion of the proximal arm of LN chromosome 17 is introgressed on the LH genomic background to assess the contribution of LN alleles on obesity features. Male and female LHLNa rats were studied, but male congenics did not significantly differ from LH in this study. Female LHLNa rats exhibited decreases in total body growth, as well as major alterations to their body composition and adiposity. The LHLNa female rats also showed decreases in metabolic rate, and a reduction in food intake. The increased adiposity in the female LHLNa rats was specific to abdominal white adipose tissue, and this phenomenon was further explained by significant hypertrophy in those adipocytes, with no evidence of adipocyte hyperplasia. Sequencing of the parental strains identified a novel frameshift mutation in the candidate gene , which is involved in transcription-coupled DNA repair, and is implicated in premature aging. The discovery of the significance of Ercc6l2 in the context of female-specific adipocyte biology could represent a novel role of DNA repair failure syndromes in obesity pathogenesis.

摘要

中心性肥胖具有遗传复杂性,在过去几十年中呈指数级增长,已成为一个关键的公共卫生问题。里昂高血压(LH)大鼠是一种特征明确的高血压模型,相对于其代谢健康的对照品系里昂正常血压(LN)大鼠,它在体重和肥胖方面也表现出自发性的显著差异。这些品系之间体重差异的潜在机制尚不清楚,因此开发了一种同源基因模型(LHLNa),即将LN 17号染色体近端臂的一部分导入LH基因组背景中,以评估LN等位基因对肥胖特征的影响。对雄性和雌性LHLNa大鼠进行了研究,但在本研究中雄性同源基因大鼠与LH大鼠没有显著差异。雌性LHLNa大鼠的全身生长出现下降,其身体组成和肥胖也发生了重大改变。LHLNa雌性大鼠的代谢率也降低,食物摄入量减少。雌性LHLNa大鼠肥胖的增加特定于腹部白色脂肪组织,这种现象可以通过这些脂肪细胞的显著肥大进一步解释,没有脂肪细胞增生的证据。对亲本品系进行测序,在候选基因中发现了一个新的移码突变,该基因参与转录偶联的DNA修复,并与早衰有关。在雌性特异性脂肪细胞生物学背景下发现Ercc6l2的重要性,可能代表了DNA修复缺陷综合征在肥胖发病机制中的新作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc2c/9263446/26fbb619e242/fgene-13-903971-g001.jpg

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