Suppr超能文献

反刍动物特异性反转录转座子塑造了牛的免疫调节进化。

Ruminant-specific retrotransposons shape regulatory evolution of bovine immunity.

机构信息

Department of Molecular, Cellular, and Developmental Biology and BioFrontiers Institute, University of Colorado Boulder, Boulder, Colorado 80309, USA.

USDA, ARS, Roman L. Hruska US Meat Animal Research Center (MARC), Clay Center, Nebraska 68933, USA.

出版信息

Genome Res. 2022 Aug 25;32(8):1474-1486. doi: 10.1101/gr.276241.121.

Abstract

Cattle are an important livestock species, and mapping the genomic architecture of agriculturally relevant traits such as disease susceptibility is a major challenge in the bovine research community. Lineage-specific transposable elements (TEs) are increasingly recognized to contribute to gene regulatory evolution and variation, but this possibility has been largely unexplored in ruminant genomes. We conducted epigenomic profiling of the type II interferon (IFN) response in bovine cells and found thousands of ruminant-specific TEs including MER41_BT and Bov-A2 elements predicted to act as IFN-inducible enhancer elements. CRISPR knockout experiments in bovine cells established that critical immune factors including and are transcriptionally regulated by TE-derived enhancers. Finally, population genomic analysis of 38 individuals revealed that a subset of polymorphic TE insertions may function as enhancers in modern cattle. Our study reveals that lineage-specific TEs have shaped the evolution of ruminant IFN responses and potentially continue to contribute to immune gene regulatory differences across modern breeds and individuals. Together with previous work in human cells, our findings demonstrate that lineage-specific TEs have been independently co-opted to regulate IFN-inducible gene expression in multiple species, supporting TE co-option as a recurrent mechanism driving the evolution of IFN-inducible transcriptional networks.

摘要

牛是一种重要的家畜物种,绘制与疾病易感性等农业相关性状的基因组结构图谱是牛研究界的主要挑战。越来越多的谱系特异性转座元件(TEs)被认为有助于基因调控进化和变异,但这种可能性在反刍动物基因组中尚未得到广泛探索。我们对牛细胞中的 II 型干扰素(IFN)反应进行了表观基因组分析,发现了数千个反刍动物特异性 TEs,包括预测为 IFN 诱导增强子元件的 MER41_BT 和 Bov-A2 元件。牛细胞中的 CRISPR 敲除实验表明,包括 和 在内的关键免疫因子受 TE 衍生增强子的转录调控。最后,对 38 个人的群体基因组分析表明,一组多态性 TE 插入可能在现代牛中作为增强子发挥作用。我们的研究表明,谱系特异性 TEs 塑造了反刍动物 IFN 反应的进化,并且可能继续为现代品种和个体的免疫基因调控差异做出贡献。与人类细胞中的先前工作一起,我们的研究结果表明,谱系特异性 TEs 已被独立地重新用于调节多种物种中的 IFN 诱导基因表达,支持 TE 重新用于驱动 IFN 诱导转录网络进化的反复机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf01/9435751/2359949e9b2b/1474f01.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验