The complex relationship between TFEB transcription factor phosphorylation and subcellular localization

R Puertollano, SM Ferguson, J Brugarolas… - The EMBO …, 2018 - embopress.org
The MiT‐TFE family of basic helix‐loop‐helix leucine‐zipper transcription factors includes
four members: TFEB, TFE 3, TFEC, and MITF. Originally described as oncogenes, these …

Type I interferon in the pathogenesis of lupus

MK Crow - The Journal of Immunology, 2014 - journals.aai.org
Investigations of patients with systemic lupus erythematosus have applied insights from
studies of the innate immune response to define IFN-I, with IFN-α as the dominant mediator …

IRF3 and type I interferons fuel a fatal response to myocardial infarction

KR King, AD Aguirre, YX Ye, Y Sun, JD Roh… - Nature medicine, 2017 - nature.com
Abstract Interferon regulatory factor 3 (IRF3) and type I interferons (IFNs) protect against
infections and cancer, but excessive IRF3 activation and type I IFN production cause …

STING activation by translocation from the ER is associated with infection and autoinflammatory disease

N Dobbs, N Burnaevskiy, D Chen, VK Gonugunta… - Cell host & …, 2015 - cell.com
STING is an ER-associated membrane protein that is critical for innate immune sensing of
pathogens. STING-mediated activation of the IFN-I pathway through the TBK1/IRF3 …

Modeling of TREX1-dependent autoimmune disease using human stem cells highlights L1 accumulation as a source of neuroinflammation

CA Thomas, L Tejwani, CA Trujillo, PD Negraes… - Cell stem cell, 2017 - cell.com
Three-prime repair exonuclease 1 (TREX1) is an anti-viral enzyme that cleaves nucleic
acids in the cytosol, preventing accumulation and a subsequent type I interferon-associated …

TFEB and TFE3: linking lysosomes to cellular adaptation to stress

N Raben, R Puertollano - Annual review of cell and …, 2016 - annualreviews.org
In recent years, our vision of lysosomes has drastically changed. Formerly considered to be
mere degradative compartments, they are now recognized as key players in many cellular …

Assessment of interferon-related biomarkers in Aicardi-Goutieres syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1 …

GI Rice, GMA Forte, M Szynkiewicz, DS Chase… - The lancet …, 2013 - thelancet.com
Summary Background Aicardi-Goutières syndrome (AGS) is an inflammatory disorder
caused by mutations in any of six genes (TREX1, RNASEH2A, RNASEH2B, RNASEH2C …

TFEB and TFE3 cooperate in the regulation of the innate immune response in activated macrophages

N Pastore, OA Brady, HI Diab, JA Martina, L Sun… - Autophagy, 2016 - Taylor & Francis
The activation of transcription factors is critical to ensure an effective defense against
pathogens. In this study we identify a critical and complementary role of the transcription …

IFI16 senses DNA forms of the lentiviral replication cycle and controls HIV-1 replication

MR Jakobsen, RO Bak, A Andersen… - Proceedings of the …, 2013 - National Acad Sciences
Replication of lentiviruses generates different DNA forms, including RNA: DNA hybrids,
ssDNA, and dsDNA. Nucleic acids stimulate innate immune responses, and pattern …

Absence of RNase H2 triggers generation of immunogenic micronuclei removed by autophagy

K Bartsch, K Knittler, C Borowski… - Human molecular …, 2017 - academic.oup.com
Hypomorphic mutations in the DNA repair enzyme RNase H2 cause the neuroinflammatory
autoimmune disorder Aicardi-Goutières syndrome (AGS). Endogenous nucleic acids are …