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. 2007 Mar 5;27(9):3353–3366. doi: 10.1128/MCB.01871-06

TABLE 2.

Comparison of Ets1ΔVII and Ets1 knockout mouse phenotypes

Parameter Result for indicated genotype
Relationshipa Reference(s)
Ets1ΔVII Ets1 knockout
ETS1 expression
    Full-length p51-Ets1 protein None Very low neomorphb S 7
    ΔVII p42-Ets1 protein High Very low neomorphb D 7
Thymus
    Cellularity 60% increased 65% reduction D 4, 7
    CD4CD8+ thymocytes Expanded Diminished D 7
    Proliferation Increased Undocumented
    Apoptosis Decreased Increased D 6, 11, 12, 40
Spleen
    Size Decreased Undocumented
    Proliferation Increased Decreased (T cells) D 40
    Apoptosis Increased Increased S 6, 40
    NK cells Present Absent D 4
    CD44hi splenocytes Diminished Expanded D 7
Systemic
    Lethality 33% pre- or perinatal 50% pre- or perinatal S 6, 7, 12
    Rapid IFN-γ secretion Diminished Diminished S 6, 7, 12
    Peripheral lymphopenia Yes Yes, but abnormal D 7, 12
a

S, similar phenotypes for Ets1ΔVII mice and (previously reported) Ets1-targeted mice; D, divergent phenotypes for these two strains.

b

The Ets1-targeted allele has been demonstrated to generate protein from in-frame splicing from exon II to exon V at ∼1 to 5% of wild-type expression levels. Also, this variant undergoes alternative splicing of exon VII to generate a neomorphic p42-Ets1 (p29).