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. 2022 Mar 16;12:815037. doi: 10.3389/fonc.2022.815037

Table 1.

Mouse models of MDS.

Genetic aberrations Techniques Reference
Gene expression
Pten/Ship deletions Pten haploinsufficient, Ship knockout (11)
Evi1 overexpression Retroviral transduction (12)
Npm1 deletion Npm1 haploinsufficient (13, 14)
Dido deletion Knockout (15)
NUP98-HOXD13 fusion Transgenic expression (Vav promoter) (1619)
SALL4B Transgenic expression (CMV promoter) (9)
Bcl2/mutant Nras Transgenic co-expression (tTA, MRP8 promoters) (20)
Arid4a Knockout (21)
Polg Knock-in of mutant (PolgA/A) (10)
MLL fusions Retroviral transduction (22)
Recurrent mutations
Transcription factors
RUNX1 Retroviral expression (D171N, S291fs) (23)
Bcor Loss-of-function mutation (24)
Epigenetic modifiers
Dnmt3a Mx1-Cre mediated ablation (25)
Tet2 Tet2:nlacZ/nGFP knockin, which results in nlacZ transcription (25)
Ezh2 Rosa26:Cre-ERT mediated ablation, followed by HSPC transplant (26)
Axsl1 Homozygous/heterozygous Asxl1:nlacZ/nGFP knockin (27)
Splicing factors
Srsf2 Mx1-Cre mediated heterozygous expression of Srsf2P95H (28)
U2af1 Doxycycline inducible heterozygous expression of U2af1S34F (29)
Sf3b1 Mx1-Cre mediated heterozygous expression of Sf3b1K700E (30)
Zrsr2 Mx1-Cre mediated ablation (28)
Chromosomal aberrations
del(5q) Deletion of Cd74-Nid67 interval (31)
BMME dysfunctions
Dicer1 Osx-Cre mediated ablation (32)
Sbds Osx-Cre mediated deletion (32, 33)
S100A9 Transgenic overexpression (34)