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. 2023 Dec 11;6:1253. doi: 10.1038/s42003-023-05546-y

Fig. 1. Expression of ThrbHAB knockin allele in the pituitary gland.

Fig. 1

a, The HAB tag on TRβ includes an HA epitope and site (target lysine underlined) for biotinylation by BirA ligase (expressed by a Rosa26BirA allele). b TRβ-HAB transcripts in pituitary RNA detected by PCR. c Expression of tagged receptors in pituitary sections detected by immunostaining for TRβ2. Thrb-KO, TRβ-deficient control. DAPI, nuclear stain shows tissue background. d Immunofluorescence analysis of anterior pituitary sections for tagged (HAB;BirA) and non-tagged receptors (control, BirA) showing nuclear signal detected with TRβ2 immunostaining. Arrowheads, representative nuclei. Alpha-tubulin cytoskeletal stain indicates cell outlines. e, f Normal thyroid gland morphology and anterior pituitary dimensions in HAB;BirA mice. Thyroid areas were measured on plastic sections. Groups, 4–6 adult males; mean ± SD (P > 0.2, one-way ANOVA). Anterior pituitary dimensions were measured for half-lobe areas in cryosections. Groups 4–6 males; mean ± SD (P > 0.16, one-way ANOVA). A.U., arbitrary units. g Serum total T4, T3 and TSH in adult males; mean ± SD. Groups, 8–12; No significant differences were detected between genotypes (P > 0.1, one-way ANOVA). h Pituitary gene RNA expression analysis by qPCR. Groups, 5–6 adult males; mean ± SD. No significant differences between genotypes (P > 0.1, one-way ANOVA).