Genomic organisation, chromosomal localisation tissue distribution and developmental regulation of the PR61/B′ regulatory subunits of protein phosphatase 2A in mice
Abstract
Protein phosphatase 2A (PP2A) is a major serine/threonine-specific phosphatase playing central roles in development, cell growth and transformation. Regulation is largely accomplished by the regulatory B subunits, which determine substrate specificity, subcellular localisation and catalytic activity. The B' family, also known as the PR61 family, is the most diverse, consisting of five genes (alpha,beta,gamma,delta and epsilon) that give rise to a number of splice variants. We deduced the sequences of the different PR61 proteins in mice and found evidence for the expression of PR61alpha, beta1, gamma1, gamma2, gamma3, delta1 and epsilon. We report the genomic organisation and localisation of the murine PR61 genes (Ppp2r5a-Ppp2r5e). This information will be useful for the future realisation of PR61 knockouts. Using Northern blotting, we examined the expression of the five PR61 isoforms in different tissues. A brain-specific function can be expected for the PR611beta protein based on the high expression levels observed in murine brain. In situ hybridisation analysis of the adult brain revealed a distinct and partially overlapping pattern of mRNA expression of the various PR61 isoforms. The PR61 mRNA expression during embryonic development was examined by Northern blotting. The PR61 transcripts were differentially expressed, suggesting a specific function for each of the PR61 proteins during embryonic development and/or adult life.
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B55γ is nearly exclusively expressed in brain and B′′α is highly expressed in heart, consistent with previous reports.
“This is probably best illustrated for B55γ (nearly exclusively expressed in brain) and B″α (highly expressed in heart), in accordance with previously published work of others [20][21][22].”
From Physiologic functions of PP2A: Lessons from genetically modified mice (2019) · cites this paper as [21]
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References 47 · Cited by 57
- Authors
- Martens, E., Stevens, I., Janssens, V., Vermeesch, J., Götz, J., Goris, J., & Van Hoof, C.
- Affiliations
- KU Leuven (BE)
- University of Zurich (CH)
- Corresponding author
- Goris, Jozef
- Venue
- Journal of Molecular Biology
- Publisher
- Elsevier BV
- Published
- 2004-02
- Volume
- 336
- Issue
- 4
- Pages
- 971-986
- ISSN
- 0022-2836 (ISSN-L)
- OpenAlex
- W2052875624
- Cited by
- 57
- References
- 47
- Citations by year
- 2025: 2 · 2023: 5 · 2022: 2 · 2021: 2 · 2020: 5 · 2019: 1 · 2018: 1 · 2017: 2 · 2016: 2 · 2015: 4 · 2014: 2 · 2013: 2 · 2012: 3
- FWCI
- 1.42
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Molecular Biology (publishedVersion)
- PubMed (publishedVersion)
- Lirias (submittedVersion)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Tyrosine Phosphatases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Signaling Pathways in Disease
- Keywords
- protein phosphatase 2A, genome organization, tissue distribution, embryonic development, splice variants, brain-specific expression, gene knockout, mice
- MeSH terms
- Amino Acid Sequence, Animals, Brain, Chromosomes, Humans, Isoenzymes, Molecular Sequence Data, Phosphoprotein Phosphatases, Tissue Distribution, Sequence Alignment, In Situ Hybridization, In Situ Hybridization, Fluorescence, Gene Expression Regulation, Developmental, Protein Subunits, Mice, Protein Phosphatase 2
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