Zalpha-domains: At the intersection between RNA editing and innate immunity


Autoria(s): Athanasiadis, Alekos
Data(s)

23/05/2016

06/11/2016

07/11/2012

Resumo

The involvement of A to I RNA editing in antiviral responses was first indicated by the observation of genomic hyper-mutation for several RNA viruses in the course of persistent infections. However, in only a few cases an antiviral role was ever demonstrated and surprisingly, it turns out that ADARs - the RNA editing enzymes - may have a prominent pro-viral role through the modulation/down-regulation of the interferon response. A key role in this regulatory function of RNA editing is played by ADAR1, an interferon inducible RNA editing enzyme. A distinguishing feature of ADAR1, when compared with other ADARs, is the presence of a Z-DNA binding domain, Zalpha. Since the initial discovery of the specific and high affinity binding of Zalpha to CpG repeats in a left-handed helical conformation, other proteins, all related to the interferon response pathway, were shown to have similar domains throughout the vertebrate lineage. What is the biological function of this domain family remains unclear but a significant body of work provides pieces of a puzzle that points to an important role of Zalpha domains in the recognition of foreign nucleic acids in the cytoplasm by the innate immune system. Here we will provide an overview of our knowledge on ADAR1 function in interferon response with emphasis on Zalpha domains.

Marie Curie IRG program: (PIRG03-GA-2008-23100); FCT grant: (PTDC/BIA-PRO/112962/2009).

Identificador

Alekos Athanasiadis, Zalpha-domains: At the intersection between RNA editing and innate immunity, Seminars in Cell & Developmental Biology, Volume 23, Issue 3, May 2012, Pages 275-280, ISSN 1084-9521, http://dx.doi.org/10.1016/j.semcdb.2011.11.001.

http://hdl.handle.net/10400.7/612

10.1016/j.semcdb.2011.11.001

Idioma(s)

eng

Publicador

Elsivier Science BV

Relação

http://www.sciencedirect.com/science/article/pii/S1084952111002242

Direitos

embargoedAccess

http://creativecommons.org/licenses/by/4.0/

Palavras-Chave #Adenosine Deaminase #Animals #DNA, Viral #DNA, Z-Form #Humans #Nucleic Acid Conformation #Protein Structure, Tertiary #RNA-Binding Proteins #Immunity, Innate #RNA Editing
Tipo

article