Generation of Amt knockout mouse by gene trapping. (A) The location of the gene-trap vector in Amt intron 2 in the ES cell line OST181110 was determined by inverse PCR. Mice carrying this mutation were generated using standard methods of blastocyst microinjection with OST181110 ES cells to generate chimeras, and germ-line transmission. LTR, long terminal repeats; SA, splicing acceptor site; Neo, neomycin phosphotransferase gene; pA, polyadenylation sequence. (B) For genotyping, mouse genomic DNA was subjected to allele-specific amplification with F, R1 and R2 primers (Supplementary Material, Table S1). A genomic fragment of 320 bp was amplified from the wild-type allele, whereas a 233 bp fragment was amplified from the Amt-mutant allele. (C) RT-PCR analysis of Amt mRNA expressed in the brain and liver of Amt-mutant mice. Primers in exon 1–2 generated a 121 bp band irrespective of mouse genotypes. RT-PCR in which either one (f2-r2) or both (f3-r3) primers were located in exons 3′ to the insertion site produced 220 and 355 bp cDNA fragments, respectively, in Amt+/+ and Amt+/− mice, but not in Amt−/−. The Amt mRNA in mice carrying the trap vector was, therefore, aberrantly spliced at the end of exon 2, resulting in truncation of Amt mRNA in Amt−/− mice.