Table 1.

Mutation analysis of NPM exon-12 sequences in hematopoietic cells from patients with NPMc+ AML


Patient and sample no.

Cell lineage

Status

Mutation type*
Patient 1    
    BM   Bone marrow bulk population   M   +CATG (960_963)  
    M1   Myeloid   M  +CATG (960_963)  
    M2   Myeloid   M   +CATG (960_963)  
    M3   Myeloid   M   +CATG (960_963)  
    E1   Erythroid   M   +CATG (960_963)  
    E2   Erythroid   M   +CATG (960_963)  
    E2   Erythroid   M   +CATG (960_963)  
    Me1   Megakaryocyte   M   +CATG (960_963)  
    Me2   Megakaryocyte   M   +CATG (960_963)  
    Me3   Megakaryocyte   M   +CATG (960_963)  
    Me4   Megakaryocyte   M   +CATG (960_963)  
Patient 2    
    M1   Myeloid   M   +TCTG (960_963)  
    M2   Myeloid   M   +TCTG (960_963)  
    M3   Myeloid   WT  NA  
    E1   Erythroid   WT  NA  
    E2   Erythroid   M   +TCTG (960_963)  
    E3   Erythroid   M   +TCTG (960_963)  
    Me1   Megakaryocyte   M   +TCTG (960_963)  
    Me2   Megakaryocyte   M   +TCTG (960_963)  
    F1   Fibroblasts   WT   NA  
    F2   Fibroblasts   WT   NA  
Patient 3    
    BM   Bone marrow bulk population   M   +TCTG (960_963)  
    Me1   Megakaryocyte   M   +TCTG (960_963)  
    Me2   Megakaryocyte   M   +TCTG (960_963)  
    Me3   Megakaryocyte   M   +TCTG (960_963)  
    Me4   Megakaryocyte   M   +TCTG (960_963)  
    V1   Vessel   WT   NA  
    V2
 
Vessel
 
WT
 
NA
 

Patient and sample no.

Cell lineage

Status

Mutation type*
Patient 1    
    BM   Bone marrow bulk population   M   +CATG (960_963)  
    M1   Myeloid   M  +CATG (960_963)  
    M2   Myeloid   M   +CATG (960_963)  
    M3   Myeloid   M   +CATG (960_963)  
    E1   Erythroid   M   +CATG (960_963)  
    E2   Erythroid   M   +CATG (960_963)  
    E2   Erythroid   M   +CATG (960_963)  
    Me1   Megakaryocyte   M   +CATG (960_963)  
    Me2   Megakaryocyte   M   +CATG (960_963)  
    Me3   Megakaryocyte   M   +CATG (960_963)  
    Me4   Megakaryocyte   M   +CATG (960_963)  
Patient 2    
    M1   Myeloid   M   +TCTG (960_963)  
    M2   Myeloid   M   +TCTG (960_963)  
    M3   Myeloid   WT  NA  
    E1   Erythroid   WT  NA  
    E2   Erythroid   M   +TCTG (960_963)  
    E3   Erythroid   M   +TCTG (960_963)  
    Me1   Megakaryocyte   M   +TCTG (960_963)  
    Me2   Megakaryocyte   M   +TCTG (960_963)  
    F1   Fibroblasts   WT   NA  
    F2   Fibroblasts   WT   NA  
Patient 3    
    BM   Bone marrow bulk population   M   +TCTG (960_963)  
    Me1   Megakaryocyte   M   +TCTG (960_963)  
    Me2   Megakaryocyte   M   +TCTG (960_963)  
    Me3   Megakaryocyte   M   +TCTG (960_963)  
    Me4   Megakaryocyte   M   +TCTG (960_963)  
    V1   Vessel   WT   NA  
    V2
 
Vessel
 
WT
 
NA
 

No negative control could be microdissected in patient 1.

M indicates mutated; WT, wild-type; +, insertion; NA, not applicable.

*

Numbering according to GenBank Accession No. NM_002520 version 4.

In these cells, only one allele was amplified.

Close Modal

or Create an Account

Close Modal
Close Modal