Molecular and Phylogenetic Analysis of Calmodulin-Dependent Protein Phosphatase (Calcineurin) Catalytic Subunit Genes
- 1 June 1992
- journal article
- research article
- Published by Mary Ann Liebert Inc in DNA and Cell Biology
- Vol. 11 (5) , 415-424
- https://doi.org/10.1089/dna.1992.11.415
Abstract
In the mammalian brain, there are multiple catalytic subunits for the Ca2+- and calmodulin-dependent protein phosphatase [also called protein phosphatase 2B (PP-2B) and calcineurin] that are derived from two structural genes. The coding sequences of these two genes are distinguished by the absence (PP2Bα1) or the presence (PP2Bα2) of an amino terminus containing polyproline. Both of these genes can produce intragenic isoforms through alternative splicing. In the present study, a potential phylogenetic relationship of these genes was inferred from analysis of genomic DNA and from studies of mRNA and protein expression. Southern blot analysis showed unique restriction fragments for both genes in seven mammalian species; however, in organisms from two nonmammalian vertebrates (chicken and lizard), hybridization was observed only for PP2Bα1. In agreement with these results, Northern blots of mammalian brain RNA showed transcripts for both genes, with about two to three times more of the PP2Bα1 mRNAs, whereas in chicken and lizard, only PP2Bα1 transcripts were detected. An analysis of protein expression by two-dimensional electrophoresis was also consistent with these findings. For the purified mammalian brain protein, eight to ten variants were observed with isoelectric points of 5.2–5.8; immunoblot analysis using anti-peptide antibodies indicated that the majority of these were PP2Bα1 forms. In chicken brain, multiple isoforms were recognized by antibodies against the PP2Bα1 forms, but no reactivity was seen with those against the PP2Bα2 forms. Taken together, these findings suggest that: (i) in mammals, the predominant catalytic subunit isoforms in brain are PP2Bα1 products and (ii) the gene for the polyproline-containing catalytic subunit of calmodulin-dependent phosphatase (PP2Bα2) may have evolved after the avian/reptilian branching point, perhaps to carry out a role(s) of particular significance in mammals.Keywords
This publication has 33 references indexed in Scilit:
- Chromosomal mapping of the human genes for the calmodulindependent protein phosphatase (calcineurin) catalytic subunitBiochemical and Biophysical Research Communications, 1991
- Calcineurin is a common target of cyclophilin-cyclosporin A and FKBP-FK506 complexesCell, 1991
- Differential distribution of the mRNA encoding two isoforms of the catalytic subunit of calcineurin in the rat brainBiochemical and Biophysical Research Communications, 1991
- The complete primary structure of calcineurin A, a calmodulin binding protein homologous with protein phosphatases 1 and 2ABiochemical and Biophysical Research Communications, 1989
- Identification, characterization, and functional correlation of calmodulin-dependent protein phosphatase in sperm.The Journal of cell biology, 1988
- A Method for Isolation of Intact, Translationally Active Ribonucleic AcidDNA, 1983
- Transcription and accurate polyadenylation in vitro of RNA from the major late adenovirus 2 transcription unitCell, 1982
- Discovery of A Ca2+‐and calmodulin‐dependent protein phosphataseFEBS Letters, 1982
- Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.Proceedings of the National Academy of Sciences, 1979
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970