| First Author | Dyson JJ | Year | 2022 |
| Journal | FASEB Bioadv | Volume | 4 |
| Issue | 4 | Pages | 273-282 |
| PubMed ID | 35415460 | Mgi Jnum | J:348684 |
| Mgi Id | MGI:7642080 | Doi | 10.1096/fba.2021-00130 |
| Citation | Dyson JJ, et al. (2022) Growth arrest of PPP2R5C and PPP2R5D double knockout mice indicates a genetic interaction and conserved function for these PP2A B subunits. FASEB Bioadv 4(4):273-282 |
| abstractText | Protein phosphatase 2A (PP2A) is a heterotrimeric phosphatase that controls a wide range of cellular functions. The catalytic activity and intracellular location of PP2A are modulated by its association with regulatory B subunits, including B56 proteins, which are encoded by five separate genes in humans and mice. The specific effects of each B56 protein on PP2A activity and function are largely unknown. As part of an effort to identify specific PP2A-B56 functions, we created knockout strains of B56beta, B56delta, and B56epsilon using CRISPR/Cas9n. We found that none of the individual B56 genes are essential for mouse survival. However, mice that have both B56delta and B56gamma inactivated (B56deltagamma-), arrest fetal development around Day E12. The hearts of B56deltagamma- mice have a single outflow vessel rather than having both an aorta and a pulmonary artery. Thus, there appears to be strong genetic interaction between B56delta and B56gamma, and together they are necessary for heart development. Of note, both these proteins have been shown to localize to the nucleus and have the most related peptide sequences of the B56 family members. Our results suggest there are B56 subfamilies, which work in conjunction to regulate specific PP2A functions. |
