Circadian transcription factor BMAL1 regulates innate immunity against select RNA viruses
Author(s) -
Majumdar Tanmay,
Dhar Jayeeta,
Patel Sonal,
Kondratov Roman,
Barik Sailen
Publication year - 2017
Publication title -
innate immunity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.921
H-Index - 69
eISSN - 1753-4267
pISSN - 1753-4259
DOI - 10.1177/1753425916681075
Subject(s) - biology , innate immune system , transcription factor , virology , immunity , transcription (linguistics) , immunology , virus , rna , microbiology and biotechnology , gene , genetics , immune system , linguistics , philosophy
BMAL1 (brain and muscle ARNT-like protein 1, also known as MOP3 or ARNT3) belongs to the family of the basic helix–loop–helix (bHLH)-PAS domain-containing transcription factors, and is a key component of the molecular oscillator that generates circadian rhythms. Here, we report that BMAL1-deficient cells are significantly more susceptible to infection by two major respiratory viruses of the Paramyxoviridae family, namely RSV and PIV3. Embryonic fibroblasts from Bmal1 –/– mice produced nearly 10-fold more progeny virus than their wild type controls. These results were supported by animal studies whereby pulmonary infection of RSV produced a more severe disease and morbidity in Bmal1 –/– mice. These results show that BMAL1 can regulate cellular innate immunity against specific RNA viruses.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom