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MXD/MIZ1 complexes activate transcription of MYC-repressed genes

https://doi.org/10.1101/842799
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/faat.1997.2371openalex-snapshot
Expression of the Immediate–Early Genes, c-fos,c-jun,and c-myc:A Comparison in Rats of Nongenotoxic Hepatocarcinogens with Noncarcinogenic Liver Mitogens
inferredcites →https://doi.org/10.1006/geno.1994.1336openalex-snapshot
Localization of the Human Mxi1 Transcription Factor Gene (MXI1) to Chromosome 10q24-q25
inferredcites →https://doi.org/10.1006/geno.1994.1496openalex-snapshot
Assignment of the Human MAD and MXI1 Genes to Chromosomes 2p12-p13 and 10q24-q25
inferredcites →https://doi.org/10.1007/s11684-018-0650-zopenalex-snapshot
The MYC transcription factor network: balancing metabolism, proliferation and oncogenesis
inferredcites →https://doi.org/10.1016/0092-8674(95)90355-0openalex-snapshot
Mad-max transcriptional repression is mediated by ternary complex formation with mammalian homologs of yeast repressor Sin3
inferredcites →https://doi.org/10.1016/j.bbrc.2011.12.140openalex-snapshot
MNT inhibits the migration of human hepatocellular carcinoma SMMC7721 cells
inferredcites →https://doi.org/10.1016/j.ccell.2018.09.001openalex-snapshot
MYC Interacts with the G9a Histone Methyltransferase to Drive Transcriptional Repression and Tumorigenesis
inferredcites →https://doi.org/10.1016/j.cell.2010.03.030openalex-snapshot
c-Myc Regulates Transcriptional Pause Release
inferredcites →https://doi.org/10.1016/j.cell.2012.03.003openalex-snapshot
MYC on the Path to Cancer
inferredcites →https://doi.org/10.1016/j.cell.2012.08.026openalex-snapshot
Transcriptional Amplification in Tumor Cells with Elevated c-Myc
inferredcites →https://doi.org/10.1016/j.cell.2012.08.033openalex-snapshot
c-Myc Is a Universal Amplifier of Expressed Genes in Lymphocytes and Embryonic Stem Cells
inferredcites →https://doi.org/10.1016/j.celrep.2016.11.025openalex-snapshot
cMyc Regulates the Size of the Premigratory Neural Crest Stem Cell Pool
inferredcites →https://doi.org/10.1016/j.cels.2018.03.003openalex-snapshot
Pan-cancer Alterations of the MYC Oncogene and Its Proximal Network across the Cancer Genome Atlas
inferredcites →https://doi.org/10.1016/j.ejca.2004.08.005openalex-snapshot
Analysis of transcripts from 17p13.3 in medulloblastoma suggests ROX/MNT as a potential tumour suppressor gene
inferredcites →https://doi.org/10.1016/j.immuni.2011.09.021openalex-snapshot
The Transcription Factor Myc Controls Metabolic Reprogramming upon T Lymphocyte Activation
inferredcites →https://doi.org/10.1016/j.molcel.2007.10.027openalex-snapshot
c-IAP1 Cooperates with Myc by Acting as a Ubiquitin Ligase for Mad1
inferredcites →https://doi.org/10.1016/j.molcel.2015.11.007openalex-snapshot
Ubiquitin-Dependent Turnover of MYC Antagonizes MYC/PAF1C Complex Accumulation to Drive Transcriptional Elongation
inferredcites →https://doi.org/10.1016/j.molcel.2019.02.031openalex-snapshot
MYC Recruits SPT5 to RNA Polymerase II to Promote Processive Transcription Elongation
inferredcites →https://doi.org/10.1016/j.tcb.2014.10.006openalex-snapshot
Taming of the beast: shaping Myc-dependent amplification
inferredcites →https://doi.org/10.1016/s0092-8674(00)80215-9openalex-snapshot
Histone Deacetylases Associated with the mSin3 Corepressor Mediate Mad Transcriptional Repression
inferredcites →https://doi.org/10.1016/s0092-8674(02)01284-9openalex-snapshot
X-Ray Structures of Myc-Max and Mad-Max Recognizing DNA
inferredcites →https://doi.org/10.1016/s0959-437x(05)80278-3openalex-snapshot
Myc and Max function as a nucleoprotein complex
inferredcites →https://doi.org/10.1016/s1097-2765(02)00633-0openalex-snapshot
Negative Regulation of the Mammalian UV Response by Myc through Association with Miz-1
inferredcites →https://doi.org/10.1038/31008openalex-snapshot
Role of Mxi1 in ageing organ systems and the regulation of normal and neoplastic growth
inferredcites →https://doi.org/10.1038/310655a0openalex-snapshot
Functional role for c-myc in mitogenic response to platelet-derived growth factor
inferredcites →https://doi.org/10.1038/35070076openalex-snapshot
Repression of p15INK4b expression by Myc through association with Miz-1
inferredcites →https://doi.org/10.1038/nature13473openalex-snapshot
Activation and repression by oncogenic MYC shape tumour-specific gene expression profiles
inferredcites →https://doi.org/10.1038/nature13537openalex-snapshot
Selective transcriptional regulation by Myc in cellular growth control and lymphomagenesis
inferredcites →https://doi.org/10.1038/ncomms11807openalex-snapshot
MYC/MIZ1-dependent gene repression inversely coordinates the circadian clock with cell cycle and proliferation
inferredcites →https://doi.org/10.1038/ncomms3535openalex-snapshot
Miz1 is required to maintain autophagic flux
inferredcites →https://doi.org/10.1038/nm0795-638openalex-snapshot
Effects of the MYC oncogene antagonist, MAD, on proliferation, cell cycling and the malignant phenotype of human brain tumour cells
inferredcites →https://doi.org/10.1038/nrc2819openalex-snapshot
MYC as a regulator of ribosome biogenesis and protein synthesis
inferredcites →https://doi.org/10.1038/nrc3984openalex-snapshot
MYC: connecting selective transcriptional control to global RNA production
inferredcites →https://doi.org/10.1038/sj.onc.1204245openalex-snapshot
Repression of transcription of the p27Kip1 cyclin-dependent kinase inhibitor gene by c-Myc
inferredcites →https://doi.org/10.1038/sj.onc.1206145openalex-snapshot
Myc represses differentiation-induced p21CIP1 expression via Miz-1-dependent interaction with the p21 core promoter
inferredcites →https://doi.org/10.1073/pnas.1705816114openalex-snapshot
PAF1 complex component Leo1 helps recruit Drosophila Myc to promoters
inferredcites →https://doi.org/10.1073/pnas.91.12.5503openalex-snapshot
Suppression of Myc, but not E1a, transformation activity by Max-associated proteins, Mad and Mxi1.
inferredcites →https://doi.org/10.1073/pnas.92.18.8488openalex-snapshot
Contrasting roles for Myc and Mad proteins in cellular growth and differentiation.
inferredcites →https://doi.org/10.1083/jcb.200908103openalex-snapshot
The Arf tumor suppressor protein inhibits Miz1 to suppress cell adhesion and induce apoptosis
inferredcites →https://doi.org/10.1093/emboj/17.3.774openalex-snapshot
Targeted disruption of the MYC antagonist MAD1 inhibits cell cycle exit during granulocyte differentiation
inferredcites →https://doi.org/10.1093/emboj/cdg442openalex-snapshot
Deletion of Mnt leads to disrupted cell cycle control and tumorigenesis
inferredcites →https://doi.org/10.1101/cshperspect.a014357openalex-snapshot
An Overview of MYC and Its Interactome
inferredcites →https://doi.org/10.1101/gad.11.1.44openalex-snapshot
Mnt, a novel Max-interacting protein is coexpressed with Myc in proliferating cells and mediates repression at Myc binding sites.
inferredcites →https://doi.org/10.1101/gad.287417.116openalex-snapshot
Nucleoporin-mediated regulation of cell identity genes
inferredcites →https://doi.org/10.1101/gad.585710openalex-snapshot
The interaction between Myc and Miz1 is required to antagonize TGFβ-dependent autocrine signaling during lymphoma formation and maintenance
inferredcites →https://doi.org/10.1101/gr.226035.117openalex-snapshot
Integrative analysis of RNA polymerase II and transcriptional dynamics upon MYC activation
inferredcites →https://doi.org/10.1126/science.aao2793openalex-snapshot
SLAM-seq defines direct gene-regulatory functions of the BRD4-MYC axis
inferredcites →https://doi.org/10.1128/mcb.01789-06openalex-snapshot
Induction of Mxi1-SRα by FOXO3a Contributes to Repression of Myc-Dependent Gene Expression
inferredcites →https://doi.org/10.1128/mcb.14.8.5510openalex-snapshot
Hierarchical Phosphorylation at N-Terminal Transformation-Sensitive Sites in c-Myc Protein Is Regulated by Mitogens and in Mitosis
inferredcites →https://doi.org/10.1128/mcb.23.21.7648-7657.2003openalex-snapshot
Miz1 Is Required for Early Embryonic Development during Gastrulation
inferredcites →https://doi.org/10.1128/mcb.24.4.1560-1569.2004openalex-snapshot
Mnt Loss Triggers Myc Transcription Targets, Proliferation, Apoptosis, and Transformation
inferredcites →https://doi.org/10.1158/0008-5472.can-05-2683openalex-snapshot
Mnt-Deficient Mammary Glands Exhibit Impaired Involution and Tumors with Characteristics of Myc Overexpression
inferredcites →https://doi.org/10.1177/1947601910378025openalex-snapshot
Myc Regulation of mRNA Cap Methylation
inferredcites →https://doi.org/10.1182/blood-2012-04-423517openalex-snapshot
High-resolution genomic profiling of chronic lymphocytic leukemia reveals new recurrent genomic alterations
inferredcites →https://doi.org/10.1186/1476-4598-9-92openalex-snapshot
Myc interacts with Max and Miz1 to repress C/EBPδ promoter activity and gene expression
inferredcites →https://doi.org/10.1242/jcs.02815openalex-snapshot
Of Myc and Mnt
inferredcites →https://doi.org/10.15252/embr.201540717openalex-snapshot
Myc coordinates transcription and translation to enhance transformation and suppress invasiveness
inferredcites →https://doi.org/10.3390/genes8020083openalex-snapshot
MNT and Emerging Concepts of MNT‐MYC Antagonism
inferredcites →https://doi.org/10.3390/genes8050142openalex-snapshot
MYC—Master Regulator of the Cancer Epigenome and Transcriptome
inferredcites →https://doi.org/10.3390/genes8060151openalex-snapshot
MYC Deregulation in Primary Human Cancers
inferredcites →https://doi.org/10.4161/cbt.4.11.2299openalex-snapshot
Mxi1 is induced by hypoxia in a HIF-1–dependent manner and protects cells from c-Myc-induced apoptosis
inferredcites →https://doi.org/10.7554/elife.15161openalex-snapshot
Different promoter affinities account for specificity in MYC-dependent gene regulation
inferredcites →https://doi.org/10.7554/elife.15161.036openalex-snapshot
Author response: Different promoter affinities account for specificity in MYC-dependent gene regulation
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