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肠道 Fabp 基因缺失导致雌雄小鼠小肠基因表达程序发生明显改变。

Distinct Alteration of Gene Expression Programs in the Small Intestine of Male and Female Mice in Response to Ablation of Intestinal Fabp Genes.

机构信息

School of Human Nutrition, McGill University, Ste. Anne de Bellevue, QC H9X 3V9, Canada.

出版信息

Genes (Basel). 2020 Aug 15;11(8):943. doi: 10.3390/genes11080943.

Abstract

Fatty acid-binding proteins (Fabps) make up a family of widely distributed cytoplasmic lipid-binding proteins. The small intestine contains three predominant Fabp species, Fabp1, Fabp2, and Fabp6. Our previous studies showed that and gene-disrupted mice exhibited sexually dimorphic phenotypes. In this study, we carried out a systematic comparative analysis of the small intestinal transcriptomes of 10 week-old wild-type (WT) and Fabp gene-disrupted male and female mice. We found that the small intestinal transcriptome of male and female mice showed key differences in the gene expression profiles that affect major biological processes. The deletion of specific Fabp genes induced unique and sex-specific changes in the gene expression program, although some differentially expressed genes in certain genotypes were common to both sexes. Functional annotation and interaction network analyses revealed that the number and type of affected pathways, as well as the sets of interacting nodes in each of the Fabp genotypes, are partitioned by sex. To our knowledge, this is the first time that sex differences were identified and categorized at the transcriptome level in mice lacking different intestinal Fabps. The distinctive transcriptome profiles of WT male and female small intestine may predetermine the nature of transcriptional reprogramming that manifests as sexually dimorphic responses to the ablation of intestinal Fabp genes.

摘要

脂肪酸结合蛋白 (Fabp) 构成了广泛分布的细胞质脂质结合蛋白家族。小肠含有三种主要的 Fabp 物种,即 Fabp1、Fabp2 和 Fabp6。我们之前的研究表明, 和 基因敲除小鼠表现出性别二态表型。在这项研究中,我们对 10 周龄野生型 (WT) 和 Fabp 基因敲除雄性和雌性小鼠的小肠转录组进行了系统比较分析。我们发现,雄性和雌性小鼠的小肠转录组在影响主要生物学过程的基因表达谱方面存在关键差异。特定 Fabp 基因的缺失诱导了基因表达程序的独特和性别特异性变化,尽管某些基因型中某些差异表达的基因在两性中都存在。功能注释和相互作用网络分析表明,受影响途径的数量和类型,以及每个 Fabp 基因型中相互作用节点的集合,按性别划分。据我们所知,这是首次在缺乏不同肠道 Fabp 的小鼠中在转录组水平上鉴定和分类性别差异。WT 雄性和雌性小肠的独特转录组谱可能预先确定了转录重编程的性质,表现为对肠道 Fabp 基因缺失的性别二态反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be54/7465894/a484cd3d887b/genes-11-00943-g001.jpg

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