| Literature DB >> 24361939 |
Lesly De Arras1, Rebecca Laws2, Sonia M Leach3, Kyle Pontis1, Jonathan H Freedman4, David A Schwartz5, Scott Alper1.
Abstract
The extent of the innate immune response is regulated by many positively and negatively acting signaling proteins. This allows for proper activation of innate immunity to fight infection while ensuring that the response is limited to prevent unwanted complications. Thus mutations in innate immune regulators can lead to immune dysfunction or to inflammatory diseases such as arthritis or atherosclerosis. To identify novel innate immune regulators that could affect infectious or inflammatory disease, we have taken a comparative genomics RNAi screening approach in which we inhibit orthologous genes in the nematode Caenorhabditis elegans and murine macrophages, expecting that genes with evolutionarily conserved function also will regulate innate immunity in humans. Here we report the results of an RNAi screen of approximately half of the C. elegans genome, which led to the identification of many candidate genes that regulate innate immunity in C. elegans and mouse macrophages. One of these novel conserved regulators of innate immunity is the mRNA splicing regulator Eftud2, which we show controls the alternate splicing of the MyD88 innate immunity signaling adaptor to modulate the extent of the innate immune response.Entities:
Keywords: C. elegans; LPS; MyD88; complex genetics; complex immunity; infection; innate immunity; macrophage; resistance; tolerance
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Year: 2013 PMID: 24361939 PMCID: PMC4063909 DOI: 10.1534/genetics.113.160499
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562