B cell Sirt1 deacetylates histone and non-histone proteins for epigenetic modulation of AID expression and the antibody response
Published 2020 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
B cell Sirt1 deacetylates histone and non-histone proteins for epigenetic modulation of AID expression and the antibody response
Authors
Keywords
-
Journal
Science Advances
Volume 6, Issue 14, Pages eaay2793
Publisher
American Association for the Advancement of Science (AAAS)
Online
2020-04-02
DOI
10.1126/sciadv.aay2793
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- TET enzymes augment activation-induced deaminase (AID) expression via 5-hydroxymethylcytosine modifications at the Aicda superenhancer
- (2019) Chan-Wang J. Lio et al. Science Immunology
- B cell activation and plasma cell differentiation are inhibited by de novo DNA methylation
- (2018) Benjamin G. Barwick et al. Nature Communications
- Metabolic reprogramming of human CD8+memory T cells through loss of SIRT1
- (2017) Mark Y. Jeng et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Myc Regulates Chromatin Decompaction and Nuclear Architecture during B Cell Activation
- (2017) Kyong-Rim Kieffer-Kwon et al. MOLECULAR CELL
- Sirtuins 1 and 2 Are Universal Histone Deacetylases
- (2016) Willie W. Hsu et al. ACS Chemical Biology
- Histone Deacetylase SIRT1 Negatively Regulates the Differentiation of Interleukin-9-Producing CD4 + T Cells
- (2016) Yu Wang et al. IMMUNITY
- Sirtuins in Epigenetic Regulation
- (2015) Hui Jing et al. CHEMICAL REVIEWS
- SIRT1 deacetylates RORγt and enhances Th17 cell generation
- (2015) Hyung W. Lim et al. JOURNAL OF EXPERIMENTAL MEDICINE
- The microRNA miR-22 inhibits the histone deacetylase HDAC4 to promote TH17 cell–dependent emphysema
- (2015) Wen Lu et al. NATURE IMMUNOLOGY
- The deacetylase Sirt1 is an essential regulator of Aire-mediated induction of central immunological tolerance
- (2015) Anna Chuprin et al. NATURE IMMUNOLOGY
- Dendritic cell SIRT1–HIF1α axis programs the differentiation of CD4+T cells through IL-12 and TGF-β1
- (2015) Guangwei Liu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Normalization of CD4 + T cell metabolism reverses lupus
- (2015) Yiming Yin et al. Science Translational Medicine
- Epigenetics of Peripheral B-Cell Differentiation and the Antibody Response
- (2015) Hong Zan et al. Frontiers in Immunology
- Histone Deacetylase Inhibitors Upregulate B Cell microRNAs That Silence AID and Blimp-1 Expression for Epigenetic Modulation of Antibody and Autoantibody Responses
- (2014) Clayton A. White et al. JOURNAL OF IMMUNOLOGY
- NF-κB Signaling Is Required for XBP1 (Unspliced and Spliced)-Mediated Effects on Antiestrogen Responsiveness and Cell Fate Decisions in Breast Cancer
- (2014) Rong Hu et al. MOLECULAR AND CELLULAR BIOLOGY
- SIRT1 promoter polymorphisms as clinical modifiers on systemic lupus erythematosus
- (2014) Camila Rosat Consiglio et al. MOLECULAR BIOLOGY REPORTS
- Resveratrol Possesses Protective Effects in a Pristane-Induced Lupus Mouse Model
- (2014) Zhuo-Long Wang et al. PLoS One
- NAD+ and sirtuins in aging and disease
- (2014) Shin-ichiro Imai et al. TRENDS IN CELL BIOLOGY
- SIRT1 and other sirtuins in metabolism
- (2014) Hung-Chun Chang et al. TRENDS IN ENDOCRINOLOGY AND METABOLISM
- Histone Deacetylase Sirtuin 1 Deacetylates IRF1 Protein and Programs Dendritic Cells to Control Th17 Protein Differentiation during Autoimmune Inflammation
- (2013) Heeyoung Yang et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Resveratrol Induces a Mitochondrial Complex I-dependent Increase in NADH Oxidation Responsible for Sirtuin Activation in Liver Cells
- (2013) Valérie Desquiret-Dumas et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Epigenetics of the antibody response
- (2013) Guideng Li et al. TRENDS IN IMMUNOLOGY
- Sirtuins mediate mammalian metabolic responses to nutrient availability
- (2012) Angeliki Chalkiadaki et al. Nature Reviews Endocrinology
- The dynamic regulation of NAD metabolism in mitochondria
- (2012) Liana Roberts Stein et al. TRENDS IN ENDOCRINOLOGY AND METABOLISM
- BCR-signalling synergizes with TLR-signalling for induction of AID and immunoglobulin class-switching through the non-canonical NF-κB pathway
- (2012) Egest J. Pone et al. Nature Communications
- MicroRNA Regulation of SIRT1
- (2012) Munekazu Yamakuchi Frontiers in Physiology
- Immunoglobulin Responses at the Mucosal Interface
- (2011) Andrea Cerutti et al. Annual Review of Immunology
- Sirtuin 1 in immune regulation and autoimmunity
- (2011) Sinyi Kong et al. IMMUNOLOGY AND CELL BIOLOGY
- SIRT1 Deacetylates the DNA Methyltransferase 1 (DNMT1) Protein and Alters Its Activities
- (2011) L. Peng et al. MOLECULAR AND CELLULAR BIOLOGY
- Interferon gamma (IFN-γ) disrupts energy expenditure and metabolic homeostasis by suppressing SIRT1 transcription
- (2011) Ping Li et al. NUCLEIC ACIDS RESEARCH
- The type III histone deacetylase Sirt1 is essential for maintenance of T cell tolerance in mice
- (2009) Jinping Zhang et al. JOURNAL OF CLINICAL INVESTIGATION
- HoxC4 binds to the promoter of the cytidine deaminase AID gene to induce AID expression, class-switch DNA recombination and somatic hypermutation
- (2009) Seok-Rae Park et al. NATURE IMMUNOLOGY
- B cell–specific and stimulation-responsive enhancers derepress Aicda by overcoming the effects of silencers
- (2009) Thinh Huy Tran et al. NATURE IMMUNOLOGY
- sirt1-null mice develop an autoimmune-like condition
- (2008) Jedon Sequeira et al. EXPERIMENTAL CELL RESEARCH
- MicroRNA-155 Suppresses Activation-Induced Cytidine Deaminase-Mediated Myc-Igh Translocation
- (2008) Yair Dorsett et al. IMMUNITY
- Sirt1 protects against high-fat diet-induced metabolic damage
- (2008) P. T. Pfluger et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started