Rm. Hoek et al., ALLELE-SPECIFIC PCR ANALYSIS FOR DETECTION OF THE GLD FAS-LIGAND POINT MUTATION, Journal of immunological methods, 210(1), 1997, pp. 109-112
The discovery of a naturally occurring missense point mutation in the
gene encoding Fas-ligand (FasL/CD95L) in generalized lymphoproliferati
ve disease (girl) mice has lead to the characterization of FasL as an
important mediator of apoptosis. Further analysis of Fast function can
be facilitated by crossing the Sld mutation onto other mouse-strains,
for example those carrying mutations affecting other molecules involv
ed in apoptosis, or disease-prone genetic backgrounds. The success of
this is dependent on a quick and reliable screening method. Here we re
port an allele-specific PCR for detection of the gld mutation. This ap
proach permits the screening of back-crossed Fl progeny within one day
, using whole blood samples as a source of genomic DNA. The technique
is fast, robust, easily learnt, and unambiguous. (C) 1997 Elsevier Sci
ence B.V.