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四核心基因型小鼠模型:评估最近发现的易位的影响。

The Four Core Genotypes mouse model: evaluating the impact of a recently discovered translocation.

机构信息

Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA, 90095, USA.

出版信息

Biol Sex Differ. 2024 Oct 31;15(1):90. doi: 10.1186/s13293-024-00665-5.

DOI:10.1186/s13293-024-00665-5
PMID:39482704
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11529163/
Abstract

The Four Core Genotypes (FCG) mouse model has become a valuable model to study the mechanistic basis for biological sex differences. This model allows discrimination between influences of gonadal sex (ovaries or testes) from those associated with genetic sex (presence of XX or XY chromosome complement). FCG mice have illuminated distinct effects of gonadal and chromosomal sex on traits ranging from brain structure and behavior to vulnerability to obesity, atherosclerosis, multiple sclerosis, Alzheimer's and other diseases. A recent study determined that the Y chromosome used in a specific line of C57BL/6J FCG mice harbors nine genes that have been duplicated from the X chromosome. This report raised concern that scores of publications that previously used the FCG model may therefore be flawed, but did not provide details regarding how studies can be evaluated for potential impact (or lack of impact) of the translocation. Here we (1) provide a practical description of the genetic translocation for researchers using the FCG model, (2) document that a majority of the studies cited in the recent report are unlikely to be affected by the translocation, (3) provide a scheme for interpreting data from studies with FCG mice harboring the Y translocation, and (4) delineate expression levels of the nine translocated genes across tissue/cell types as a filter for evaluating their potential involvement in specific phenotypes.

摘要

四核心基因型(FCG)小鼠模型已成为研究生物学性别差异的机制基础的有价值模型。该模型允许区分性腺性别(卵巢或睾丸)与遗传性别(XX 或 XY 染色体组成)相关的影响。FCG 小鼠阐明了性腺和染色体性别对从大脑结构和行为到肥胖、动脉粥样硬化、多发性硬化症、阿尔茨海默病和其他疾病易感性等特征的不同影响。最近的一项研究确定,在特定的 C57BL/6J FCG 小鼠品系中使用的 Y 染色体携带有九个从 X 染色体重复的基因。这一报告引起了人们的关注,即之前使用 FCG 模型的大量出版物可能因此存在缺陷,但没有提供关于如何评估研究可能受到易位影响(或缺乏影响)的详细信息。在这里,我们(1)为使用 FCG 模型的研究人员提供了遗传易位的实用描述,(2)证明了最近报告中引用的大多数研究不太可能受到易位的影响,(3)提供了一种解释来自携带 Y 易位的 FCG 小鼠的研究数据的方案,以及(4)描绘了九个易位基因在组织/细胞类型中的表达水平,作为评估它们在特定表型中潜在参与的过滤器。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9180/11529163/b896e1d021a1/13293_2024_665_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9180/11529163/f049f16811f0/13293_2024_665_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9180/11529163/08d82af0429d/13293_2024_665_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9180/11529163/b896e1d021a1/13293_2024_665_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9180/11529163/f049f16811f0/13293_2024_665_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9180/11529163/08d82af0429d/13293_2024_665_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9180/11529163/b896e1d021a1/13293_2024_665_Fig3_HTML.jpg

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