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. 2015 Aug 17;35(18):3244–3253. doi: 10.1128/MCB.00074-15

FIG 2.

FIG 2

Expression of steroidogenic enzyme genes in wild-type and Celf1−/− males. (A) Pathway of sex steroid synthesis. The CYP17A1 protein has two sequential enzymatic activities, but the intermediate products were omitted for clarity. (B) Quantification of the indicated mRNAs by RT-qPCR in the testes of wild-type and Celf1−/− littermates. (C) (Left) Representative Western blot of testis extracts from Celf1−/− or Celf1+/+ mice with antibodies against HSD3B6 and TUBB (loading control). (Right) Quantification of the HSD3B6/TUBB ratios from Western blots performed with 7 wild-type and Celf1−/− testis extracts. (D) Aromatase activities in microsomal fractions of testes measured by a tritiated-water release assay. (E) Quantification of the abundance of Cyp19a1 pre-mRNA using primers directed against the indicated intron (I)-exon (E) junctions. In all panels, gray bars represent wild-type mice, and white bars represent Celf1−/− mice. The P values of Wilcoxon signed rank tests below 0.1 are shown. n, number of pairs of wild-type and Celf1−/− littermates.