| First Author | Kobayashi-Tanabe M | Year | 2023 |
| Journal | Brain Res | Volume | 1800 |
| Pages | 148188 | PubMed ID | 36463953 |
| Mgi Jnum | J:334057 | Mgi Id | MGI:7412629 |
| Doi | 10.1016/j.brainres.2022.148188 | Citation | Kobayashi-Tanabe M, et al. (2022) Characterization of a WD-repeat family protein WDR3 in the brain of WDR3 hetero knockout mice. Brain Res 1800:148188 |
| abstractText | The nuclear protein WDR3 is a member of the WD-repeat family and is a component of the 18S pre-rRNA processing complex. However, the expression and function of WDR3 in the brain remains unknown. To characterize WDR3 in the adult mouse brain, we developed Wdr3 heterozygous knockout (WDR3-HKO) mice. Notably, no homozygous Wdr3 knockout mice were born, suggesting that complete absence of WDR3 causes lethal abnormalities during embryogenesis. Brain Wdr3 mRNA expression was significantly reduced to 60% in the WDR3-HKO mice compared to wild type (WT) mice, while the expression of 18S rRNA did not decline. Using immunohistochemistry and X-gal staining, we demonstrated that WDR3 is widely expressed in the mouse brain, especially in the hippocampus, habenular nucleus, and cerebellum. We observed no differences in body weight during adulthood or developmental weight gain between the WDR3-HKO and WT mice. Interestingly, WDR3-HKO mice exhibited a slight but significant increase in spontaneous locomotor activity compared to WT littermates. In conclusion, the WDR3-HKO mice showed no significant phenotypic changes. Further studies are required to explore the behavioral characteristics of WDR3-HKO mice. |
