Abstract 2211: A comparative analysis of the cis-regulatory landscape between human and mouse

Abstract

Abstract As the premier model organism in biomedical research, the laboratory mouse shares the vast majority of protein-coding genes with humans, but significant differences exist between the two mammals, posing considerable challenges in the study and modeling of human diseases. The mouse ENCODE consortium applied the same high throughput approaches as the human ENCODE studies and produced more than1000 coordinated datasets in over 100 mouse cell types and tissues and greatly expanded the annotation of the mouse genome. By comparative analysis with the human genome, we found that although the majority of gene expression and cis-regulatory elements are conserved between the two species, a large degree of gene regulatory elements appear to be species-specific and these species-specific elements are enriched for genes involved in immune system and metabolic process, suggesting that different gene pathways evolve at distinct rates. Moreover, we found that species-specific elements are also enriched for repetitive DNA elements such LTR and SINE, which we hypothesize to be responsible generating the species-specific elements. Finally, we developed a novel computational method to study the functional conservation between two species without requiring perfectly matched cell lines or tissues. The result confirms that cis-elements with different evolutionary rates are associated distinct biological pathways and reveals the complex driving forces in the evolution of cis-regulatory landscape in mammals. Note: This abstract was not presented at the meeting. Citation Format: Feng Yue, Yin Shen, Zhen Ye, Bing Ren. A comparative analysis of the cis-regulatory landscape between human and mouse. [abstract]. In: Proceedings of the 106th Annual Meeting of the American Association for Cancer Research; 2015 Apr 18-22; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2015;75(15 Suppl):Abstract nr 2211. doi:10.1158/1538-7445.AM2015-2211