Implications of somatic mutations in the AML1 gene in radiation-associated and therapy-related myelodysplastic syndrome/acute myeloid leukemia by Hironori.

Slides:



Advertisements
Similar presentations
Up-Regulation of Activating Transcription Factor-5 Suppresses SAP Expression to Activate T Cells in Hemophagocytic Syndrome Associated with Epstein-Barr.
Advertisements

Constitutive NF-κB activation by the t(11;18)(q21;q21) product in MALT lymphoma is linked to deregulated ubiquitin ligase activity  Honglin Zhou, Ming-Qing.
Figure 3. Activation of Wild-Type and Point-Mutated MMP-9 Promoter Constructs by IL-1β A, Schematic representation of the different 1.3-kb MMP-9-luciferase.
HMGA2 is a SUMOylation target.
by Hanna S. Radomska, Anne B
Heterozygous PU.1 mutations are associated with acute myeloid leukemia
A novel SHP-1/Grb2–dependent mechanism of negative regulation of cytokine-receptor signaling: contribution of SHP-1 C-terminal tyrosines in cytokine signaling.
Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair by Luca Colnaghi, Mathew.
by Toshibumi Shimokawa, and Chisei Ra
The Role of Transcription Factor PU
by Hong Hao, Huiling Qi, and Manohar Ratnam
Volume 11, Issue 6, Pages (June 2003)
Large Hepatitis Delta Antigen Modulates Transforming Growth Factor-β Signaling Cascades: Implication of Hepatitis Delta Virus–Induced Liver Fibrosis 
CD74 induces TAp63 expression leading to B-cell survival
MafB negatively regulates RANKL-mediated osteoclast differentiation
Physical and functional link of the leukemia-associated factors AML1 and PML by Lan Anh Nguyen, Pier Paolo Pandolfi, Yukiko Aikawa, Yusuke Tagata, Misao.
Lyn Physically Associates With the Erythropoietin Receptor and May Play a Role in Activation of the Stat5 Pathway by Hiroshi Chin, Ayako Arai, Hiroshi.
Volume 5, Issue 4, Pages (April 2004)
Tax ubiquitylation and sumoylation control critical cytoplasmic and nuclear steps of NF-κB activation by Rihab Nasr, Estelle Chiari, Marwan El-Sabban,
by Sanjai Sharma, and Alan Lichtenstein
by Katriina J. Peltola, Kirsi Paukku, Teija L. T
Pirh2 promotes p73 ubiquitination in vivo.
by Wu-Guo Deng, Ying Zhu, and Kenneth K. Wu
EP4 promoter activity is induced by sulindac sulfide in T98G cells.
Phosphorylation of NF-κB p65 by PKA Stimulates Transcriptional Activity by Promoting a Novel Bivalent Interaction with the Coactivator CBP/p300  Haihong.
by Juan M. Cárcamo, Oriana Bórquez-Ojeda, and David W. Golde
Histone deacetylase 3 associates with and represses the transcription factor GATA-2 by Yukiyasu Ozawa, Masayuki Towatari, Shinobu Tsuzuki, Fumihiko Hayakawa,
Attenuation of AML1-ETO cellular dysregulation correlates with increased leukemogenic potential by Russell C. DeKelver, Ming Yan, Eun-Young Ahn, Wei-Jong.
High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia by.
by Shrikanth P. Hegde, JingFeng Zhao, Richard A. Ashmun, and Linda H
Lipopolysaccharide activation of the MEK-ERK1/2 pathway in human monocytic cells mediates tissue factor and tumor necrosis factor α expression by inducing.
IFN-γ Upregulates Expression of the Mouse Complement C1rA Gene in Keratinocytes via IFN-Regulatory Factor-1  Sung June Byun, Ik-Soo Jeon, Hyangkyu Lee,
The interferon regulatory factor ICSBP/IRF-8 in combination with PU
Volume 16, Issue 6, Pages (December 2004)
HES1 is a novel interactor of the Fanconi anemia core complex
Rose-Anne Romano, Barbara Birkaya, Satrajit Sinha 
by Kentson Lam, Alexander Muselman, Randal Du, Yuka Harada, Amanda G
ASK1 Is Essential for JNK/SAPK Activation by TRAF2
C-MYC induces the transcription of LIG3 and PARP1 in FLT3/ITD- and BCR-ABL1–positive cells. c-MYC induces the transcription of LIG3 and PARP1 in FLT3/ITD-
Identification and Characterization of an IκB Kinase
Transcriptional Control of the Mouse Col7a1 Gene in Keratinocytes: Basal and Transforming Growth Factor-β Regulated Expression  Michael Naso, Jouni Uitto,
Volume 130, Issue 4, Pages (August 2007)
Volume 130, Issue 4, Pages (April 2006)
Ras Induces Mediator Complex Exchange on C/EBPβ
SUMO Promotes HDAC-Mediated Transcriptional Repression
Slicing-Independent RISC Activation Requires the Argonaute PAZ Domain
Volume 93, Issue 5, Pages (May 1998)
Colin Kwok, Bernd B. Zeisig, Shuo Dong, Chi Wai Eric So  Cancer Cell 
Transcriptional Regulation of ATP2C1 Gene by Sp1 and YY1 and Reduced Function of its Promoter in Hailey–Hailey Disease Keratinocytes  Hiroshi Kawada,
p53DINP1, a p53-Inducible Gene, Regulates p53-Dependent Apoptosis
Keratinocyte growth factor promotes goblet cell differentiation through regulation of goblet cell silencer inhibitor  Dai Iwakiri, Daniel K. Podolsky 
Andrei Kuzmichev, Thomas Jenuwein, Paul Tempst, Danny Reinberg 
Analyses of the Effects That Disease-Causing Missense Mutations Have on the Structure and Function of the Winged-Helix Protein FOXC1  Ramsey A. Saleem,
SUMO-1 Modification Represses Sp3 Transcriptional Activation and Modulates Its Subnuclear Localization  Sarah Ross, Jennifer L Best, Leonard I Zon, Grace.
Volume 25, Issue 5, Pages (March 2007)
Dan Yu, Rongdiao Liu, Geng Yang, Qiang Zhou  Cell Reports 
Hua Gao, Yue Sun, Yalan Wu, Bing Luan, Yaya Wang, Bin Qu, Gang Pei 
Defining the Regulatory Elements in the Proximal Promoter of ΔNp63 in Keratinocytes: Potential Roles for Sp1/Sp3, NF-Y, and p63  Rose-Anne Romano, Barbara.
Figure 4 DNM1 mutations affect protein levels and self-dimerization (A) HeLa cells were transfected with green fluorescent protein (GFP)-tagged mutant.
Dissociation of HP1α from H3K9me3 is critical to potentiation of steady-state ATM activity. Dissociation of HP1α from H3K9me3 is critical to potentiation.
Transcriptional Regulation by p53 through Intrinsic DNA/Chromatin Binding and Site- Directed Cofactor Recruitment  Joaquin M Espinosa, Beverly M Emerson 
Key functional sites of SPINDLIN1 could be phosphorylated by Aurora-A.
Constitutive NF-κB activation by the t(11;18)(q21;q21) product in MALT lymphoma is linked to deregulated ubiquitin ligase activity  Honglin Zhou, Ming-Qing.
Mapping the Pirh2 and p73 interaction sites.
A Splicing-Independent Function of SF2/ASF in MicroRNA Processing
Pirh2 represses p73-dependent transactivation.
The interaction of PALB2 with BRCA1 is required for the assembly of PALB2, BRCA2, and RAD51 nuclear foci. The interaction of PALB2 with BRCA1 is required.
The adaptor protein Lad associates with the G protein β subunit and mediates chemokine-dependent T-cell migration by Dongsu Park, Inyoung Park, Deogwon.
Volume 6, Issue 3, Pages (March 1997)
Acetylation Regulates Transcription Factor Activity at Multiple Levels
Presentation transcript:

Implications of somatic mutations in the AML1 gene in radiation-associated and therapy-related myelodysplastic syndrome/acute myeloid leukemia by Hironori Harada, Yuka Harada, Hideo Tanaka, Akiro Kimura, and Toshiya Inaba Blood Volume 101(2):673-680 January 15, 2003 ©2003 by American Society of Hematology

Summary of the AML1 point mutations identified in this study Summary of the AML1 point mutations identified in this study.Horizontal bars diagrammatically show AML1 (453 aa) including the Runt domain (50-177; shaded boxes). Summary of the AML1 point mutations identified in this study.Horizontal bars diagrammatically show AML1 (453 aa) including the Runt domain (50-177; shaded boxes). The numbers in the left-hand column indicate the case numbers (1-13) described in Tables 2, 3, and 4. The regions where the point mutations are mapped in the runt domain are described in the right-hand column. Mutant numbers are used in the next figures. Hironori Harada et al. Blood 2003;101:673-680 ©2003 by American Society of Hematology

Abilities of AML1 mutants to bind DNA and to heterodimerize with CBFβ Abilities of AML1 mutants to bind DNA and to heterodimerize with CBFβ.(A) DNA binding potential of AML1 mutants analyzed by EMSA using nuclear extract from Cos-7 cells transfected with wild-type AML1 or mutated AML1 expression plasmid vectors. Abilities of AML1 mutants to bind DNA and to heterodimerize with CBFβ.(A) DNA binding potential of AML1 mutants analyzed by EMSA using nuclear extract from Cos-7 cells transfected with wild-type AML1 or mutated AML1 expression plasmid vectors. The oligonucleotides used as competitors were as follows: “W” containing one wild-type AML1 binding site (CGAGTATTGTGGTTAATACG); “M” containing one mutated AML1 binding site (CGAGTATTGTTAGTAATACG). (B) Heterodimerization ability of AML1 mutants with CBFβ. Cos-7 cells were cotransfected with an expression vector containing CBFβ cDNA and those containing either wild-type AML1 or mutated AML1 cDNA. Cell lysates were immunoprecipitated (IP) with anti–FLAG M2 antibody, and then proteins were detected by immunoblot analysis (WB) using anti-CBFβ antibody (top). The expression levels of CBFβ and AML1 in total cell lysates were detected by immunoblot analysis with anti-CBFβ antibody (upper middle) and anti–FLAG M2 antibody (lower middle), respectively. The AML1 expression levels also were analyzed by anti-AML1 antibody (bottom). The numbers of AML1 mutants (1-10) are shown in Figure 1. Hironori Harada et al. Blood 2003;101:673-680 ©2003 by American Society of Hematology

Transcriptional potential of AML1 mutants Transcriptional potential of AML1 mutants.(A) Transcriptional activities of the AML1 mutants in HeLa cells. Transcriptional potential of AML1 mutants.(A) Transcriptional activities of the AML1 mutants in HeLa cells. Cells were transfected with 5 μg of pM-CSF-R-luc, 3 μg of FLAG-tagged AML1 or AML1 mutant expression vector, 1 μg of the CBFβ expression vector, and 0.25 μg of pRL-tk as an internal control to normalize luciferase activities for transfection efficiency. The levels of expression of CBFβ and AML1 were detected by Western blot analysis with anti-CBFβ antibody (middle) and anti–FLAG M2 antibody (bottom), respectively. (B) Transcriptional activities of the AML1 mutants in U937 cells. Cells were transfected with 2 μg of pM-CSF-R-luc reporter plasmid, an indicated amount of AML1 expression constructs, and 0.2 μg of pRL-tk as an internal control that normalizes luciferase activities for transfection efficiency. The expression vector containing wild-type AML1 (0.2 μg) was cotransfected with increasing doses (0, 0.1, 0.2, and 0.4 μg) of expression vectors containing various AML1 mutants. Each value represents the mean of 3 independent experiments. The error bars indicate the mean ± SD. The numbers of AML1 mutants (1-10) are shown in Figure 1. Hironori Harada et al. Blood 2003;101:673-680 ©2003 by American Society of Hematology

Schematic diagram of the incidence of radiation-induced cancer after atomic bombing.Adapted with permission from Kato and Shimizu.29. Schematic diagram of the incidence of radiation-induced cancer after atomic bombing.Adapted with permission from Kato and Shimizu.29 Hironori Harada et al. Blood 2003;101:673-680 ©2003 by American Society of Hematology