Identification of a Novel Protein Phosphatase 2A Regulatory Subunit Highly Expressed in Muscle

Differential association of regulatory B subunits with a core heterodimer, composed of a catalytic (C) and a structural (A) subunit, is an important mechanism that regulates protein phosphatase 2A (PP2A). We have isolated and characterized three novel cDNAs related to the B′ subunit of bovine cardiac PP2A. Two human (B′α1 and B′α2) and a mouse (B′α3) cDNA encode for alternatively spliced variants of the B′ subunit. The deduced primary sequences of these clones contain 12 of 15 peptides derived from the purified bovine B′ subunit. Differences between the deduced sequences of the B′α splice variants and the cardiac peptide sequences suggest the existence of multiple isoforms of the B′ subunit. Comparison of the protein and nucleotide sequences of the cloned cDNAs show that all three forms of B′α diverge at a common splice site near the 3′-end of the coding regions. Northern blot and reverse transcription-polymerase chain reaction analyses revealed that the B′α transcripts (4.3-4.4 kb) are widely expressed and very abundant in heart and skeletal muscle. The expressed human and mouse B′α proteins readily associated with the PP2A core enzyme in both in vitro and in vivo complex formation assays. Immunofluorescence microscopy revealed that epitope-tagged B′α was localized in both the cytosol and nuclei of transiently transfected cells. The efficiency of binding of all three expressed proteins to a glutathione S-transferase-A subunit fusion protein was greatly enhanced by the addition of the C subunit. Expression of the B′α subunits in insect Sf9 cells resulted in formation of AC•B′α heterotrimers with the endogenous insect A and C subunits. These results show that the B′ subunit, which is the predominant regulatory subunit in cardiac PP2A, is a novel protein whose sequence is unrelated to other PP2A regulatory subunits. The nuclear localization of expressed B′α suggests that some variants of the B′ subunit are involved in the nuclear functions of PP2A. Differential association of regulatory B subunits with a core heterodimer, composed of a catalytic (C) and a structural (A) subunit, is an important mechanism that regulates protein phosphatase 2A (PP2A). We have isolated and characterized three novel cDNAs related to the B′ subunit of bovine cardiac PP2A. Two human (B′α1 and B′α2) and a mouse (B′α3) cDNA encode for alternatively spliced variants of the B′ subunit. The deduced primary sequences of these clones contain 12 of 15 peptides derived from the purified bovine B′ subunit. Differences between the deduced sequences of the B′α splice variants and the cardiac peptide sequences suggest the existence of multiple isoforms of the B′ subunit. Comparison of the protein and nucleotide sequences of the cloned cDNAs show that all three forms of B′α diverge at a common splice site near the 3′-end of the coding regions. Northern blot and reverse transcription-polymerase chain reaction analyses revealed that the B′α transcripts (4.3-4.4 kb) are widely expressed and very abundant in heart and skeletal muscle. The expressed human and mouse B′α proteins readily associated with the PP2A core enzyme in both in vitro and in vivo complex formation assays. Immunofluorescence microscopy revealed that epitope-tagged B′α was localized in both the cytosol and nuclei of transiently transfected cells. The efficiency of binding of all three expressed proteins to a glutathione S-transferase-A subunit fusion protein was greatly enhanced by the addition of the C subunit. Expression of the B′α subunits in insect Sf9 cells resulted in formation of AC•B′α heterotrimers with the endogenous insect A and C subunits. These results show that the B′ subunit, which is the predominant regulatory subunit in cardiac PP2A, is a novel protein whose sequence is unrelated to other PP2A regulatory subunits. The nuclear localization of expressed B′α suggests that some variants of the B′ subunit are involved in the nuclear functions of PP2A.