SRSF1 facilitates cytosolic DNA-induced production of type i interferons recognized by RIG-I

7Citations
Citations of this article
21Readers
Mendeley users who have this article in their library.

Abstract

Background: Evidence has shown that psoriasis is closely associated with infection; however, the mechanism of this association remains unclear. In mammalian cells, viral or bacterial infection is accompanied by the release of cytosolic DNA, which in turn triggers the production of type-I interferons (IFNs). Type I IFNs and their associated genes are significantly upregulated in psoriatic lesions. RIG-I is also highly upregulated in psoriatic lesions and is responsible for IFN production. However, RIG-I mediated regulatory signaling in psoriasis is poorly understood. Methods: We screened a cDNA library and identified potential RIG-I interacting partners that may play a role in psoriasis. Results: We found that serine/arginine-rich splicing factor 1 (SRSF1) could specifically interact with RIG-I to facilitate RIG-I mediated production of type-I IFN that is triggered by cytosolic DNA. We found SRSF1 associates with RNA polymerase III and RIG-I in a DNA-dependent manner. In addition, treatment with a TNFα inhibitor downregulated SRSF1 expression in peripheral blood mononuclear cells (PBMCs) from psoriasis vulgaris patients. Discussion: Based on the abundance of pathogenic cytosolic DNA that is detected in psoriatic lesions, our finding that RIG-I interacts with SRSF1 to regulate type-I IFN production reveals a critical link regarding how cytosolic DNA specifically activates aberrant IFN expression. These data may provide new therapeutic targets for the treatment of psoriasis.

Cite

CITATION STYLE

APA

Xue, F., Li, X., Zhao, X., Wang, L., Liu, M., Shi, R., & Zheng, J. (2015). SRSF1 facilitates cytosolic DNA-induced production of type i interferons recognized by RIG-I. PLoS ONE, 10(2). https://doi.org/10.1371/journal.pone.0115354

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free