Research Article

Characterisation of APS-1 Experimental Models Is Crucial for Development of Novel Therapies

Table 1

APS-1 mouse models.

BackgroundPeltonen groupMathis groupMatsumoto groupScott group
C57BL/6C57BL/6NOD/LtJBALB/cJSJL/JC57BL/6NOD/Shi JicC57BL/6

DesignNeo cassette insertion in exon 6Cre-lox-mediated deletion of exon 2Backcrossed with Aire−/− C57BL/6Backcrossed with Aire−/− C57BL/6Backcrossed with Aire−/− C57BL/6Neo cassette insertion replacing exons 5-12Backcrossed with Aire−/− C57BL/6Cre-lox-mediated deletion of exon 8

Predicted mRNAExon 1-5Exon 1Exons 1-4Exons 1-7

Predicted protein domainsHSR, NLS, premature SANDPremature HSRHSR, NLSHSR, NLS, SAND, premature PHD-1

Major human equivalent mutationC889TR257XNAd1094-1106 del13

References[16][17, 19][21, 23][22]