Fig. 7: Generation and basic characterization of the Speg3A-knockin mice. | Nature Communications

Fig. 7: Generation and basic characterization of the Speg3A-knockin mice.

From: A PKB-SPEG signaling nexus links insulin resistance with diabetic cardiomyopathy by regulating calcium homeostasis

Fig. 7

a Diagram of strategy for generation of the Speg3A-knockin mice. The cluster of serine/threonine residues Ser2461/Ser2462/Thr2463 (the surrounding sequence is LAVRRRLsstLERL, Ser2461/Ser2462/Thr2463 shown in lower case, and numbering is according to NP_031489.4) on SPEG was substituted to alanine by point mutagenesis. b Oral glucose tolerance test in the male Speg3A-knockin mice and wild-type littermates (9-month-old). n = 5 (WT) and 6 (Speg3A). p = 0.050 (0 min), 0.799 (15 min), 0.996 (30 min), 0.718 (45 min), 0.244 (60 min), and 0.134 (120 min). c Levels of glucose, non-esterified fatty acids (NEFA), triglycerides (TG) and total cholesterol (TC) were determined in the blood of male Speg3A-knockin mice and wild-type littermates (8-month-old) after an overnight fast. n = 15 (WT) and 11 (Speg3A). p = 0.270 (blood glucose), 0.317 (plasma NEFA), 0.819 (plasma TG), and 0.412 (plasma TC). d SPEG expression and PAS-reactive phosphorylation in the heart of WT and Speg3A-knockin mice in response to insulin. The data are given as the mean ± SEM. Statistical analyses were carried out using two-sided t-test. Source data are provided as a Source Data file.

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