The three Type 2A protein phosphatases, PP2Ac, PP4c and PP6c, are differentially regulated by Alpha4
Alpha4 is a non-canonical regulatory subunit of Type 2A protein phosphatases that interacts directly with the phosphatase catalytic subunits (PP2Ac, PP4c, and PP6c) and is upregulated in a variety of cancers. Alpha4 modulates phosphatase expression levels and activity, but the molecular mechanism of...
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Veröffentlicht in: | Biochemical and biophysical research communications 2016-06, Vol.475 (1), p.64-69 |
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description | Alpha4 is a non-canonical regulatory subunit of Type 2A protein phosphatases that interacts directly with the phosphatase catalytic subunits (PP2Ac, PP4c, and PP6c) and is upregulated in a variety of cancers. Alpha4 modulates phosphatase expression levels and activity, but the molecular mechanism of this regulation is unclear, and the extent to which the various Type 2A catalytic subunits associate with Alpha4 is also unknown. To determine the relative fractions of the Type 2A catalytic subunits associated with Alpha4, we conducted Alpha4 immunodepletion experiments in HEK293T cells and found that a significant fraction of total PP6c is associated with Alpha4, whereas a minimal fraction of total PP2Ac is associated with Alpha4. To facilitate studies of phosphatases in the presence of mutant or null Alpha4 alleles, we developed a facile and rapid method to simultaneously knockdown and rescue Alpha4 in tissue culture cells. This approach has the advantage that levels of endogenous Alpha4 are dramatically reduced by shRNA expression thereby simplifying interpretation of mutant phenotypes. We used this system to show that knockdown of Alpha4 preferentially impacts the expression of PP4c and PP6c compared to expression levels of PP2Ac. |
doi_str_mv | 10.1016/j.bbrc.2016.05.036 |
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Alpha4 modulates phosphatase expression levels and activity, but the molecular mechanism of this regulation is unclear, and the extent to which the various Type 2A catalytic subunits associate with Alpha4 is also unknown. To determine the relative fractions of the Type 2A catalytic subunits associated with Alpha4, we conducted Alpha4 immunodepletion experiments in HEK293T cells and found that a significant fraction of total PP6c is associated with Alpha4, whereas a minimal fraction of total PP2Ac is associated with Alpha4. To facilitate studies of phosphatases in the presence of mutant or null Alpha4 alleles, we developed a facile and rapid method to simultaneously knockdown and rescue Alpha4 in tissue culture cells. This approach has the advantage that levels of endogenous Alpha4 are dramatically reduced by shRNA expression thereby simplifying interpretation of mutant phenotypes. We used this system to show that knockdown of Alpha4 preferentially impacts the expression of PP4c and PP6c compared to expression levels of PP2Ac.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2016.05.036</identifier><identifier>PMID: 27169767</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adaptor Proteins, Signal Transducing ; alleles ; Alpha4 ; Catalytic Domain ; Gene Knockdown Techniques ; HEK293 Cells ; HeLa Cells ; Humans ; Intracellular Signaling Peptides and Proteins - analysis ; Intracellular Signaling Peptides and Proteins - genetics ; Intracellular Signaling Peptides and Proteins - metabolism ; Lentiviral expression ; Molecular Chaperones ; mutants ; neoplasms ; phenotype ; Phosphoprotein Phosphatases - analysis ; Phosphoprotein Phosphatases - metabolism ; Protein Phosphatase 2 - analysis ; Protein Phosphatase 2 - metabolism ; Protein phosphatase 2A (PP2A) ; Protein phosphatases ; protein subunits ; rapid methods ; tissue culture</subject><ispartof>Biochemical and biophysical research communications, 2016-06, Vol.475 (1), p.64-69</ispartof><rights>2016</rights><rights>Copyright © 2016. Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-b8fcaa22c8f12db13f862c297043ac147f9569001925b9141f41796bd581d9253</citedby><cites>FETCH-LOGICAL-c488t-b8fcaa22c8f12db13f862c297043ac147f9569001925b9141f41796bd581d9253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bbrc.2016.05.036$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,777,781,882,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27169767$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LeNoue-Newton, Michele L.</creatorcontrib><creatorcontrib>Wadzinski, Brian E.</creatorcontrib><creatorcontrib>Spiller, Benjamin W.</creatorcontrib><title>The three Type 2A protein phosphatases, PP2Ac, PP4c and PP6c, are differentially regulated by Alpha4</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Alpha4 is a non-canonical regulatory subunit of Type 2A protein phosphatases that interacts directly with the phosphatase catalytic subunits (PP2Ac, PP4c, and PP6c) and is upregulated in a variety of cancers. Alpha4 modulates phosphatase expression levels and activity, but the molecular mechanism of this regulation is unclear, and the extent to which the various Type 2A catalytic subunits associate with Alpha4 is also unknown. To determine the relative fractions of the Type 2A catalytic subunits associated with Alpha4, we conducted Alpha4 immunodepletion experiments in HEK293T cells and found that a significant fraction of total PP6c is associated with Alpha4, whereas a minimal fraction of total PP2Ac is associated with Alpha4. To facilitate studies of phosphatases in the presence of mutant or null Alpha4 alleles, we developed a facile and rapid method to simultaneously knockdown and rescue Alpha4 in tissue culture cells. This approach has the advantage that levels of endogenous Alpha4 are dramatically reduced by shRNA expression thereby simplifying interpretation of mutant phenotypes. We used this system to show that knockdown of Alpha4 preferentially impacts the expression of PP4c and PP6c compared to expression levels of PP2Ac.</description><subject>Adaptor Proteins, Signal Transducing</subject><subject>alleles</subject><subject>Alpha4</subject><subject>Catalytic Domain</subject><subject>Gene Knockdown Techniques</subject><subject>HEK293 Cells</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Intracellular Signaling Peptides and Proteins - analysis</subject><subject>Intracellular Signaling Peptides and Proteins - genetics</subject><subject>Intracellular Signaling Peptides and Proteins - metabolism</subject><subject>Lentiviral expression</subject><subject>Molecular Chaperones</subject><subject>mutants</subject><subject>neoplasms</subject><subject>phenotype</subject><subject>Phosphoprotein Phosphatases - analysis</subject><subject>Phosphoprotein Phosphatases - metabolism</subject><subject>Protein Phosphatase 2 - analysis</subject><subject>Protein Phosphatase 2 - metabolism</subject><subject>Protein phosphatase 2A (PP2A)</subject><subject>Protein phosphatases</subject><subject>protein subunits</subject><subject>rapid methods</subject><subject>tissue culture</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU1r3DAQFaWl2Sb9Az0UHXuIXY1WliUohSX0IxBoDhvoTcjSONbitV3JG9h_H5lNQ3tpmcOMNG8eb-YR8g5YCQzkx13ZNNGVPNclq0q2li_ICphmBQcmXpIVY0wWXMPPM_ImpR1jAELq1-SM1yB1LesV8dsO6dxFRLo9Tkj5hk5xnDEMdOrGNHV2tgnTJb295Ru3JOGoHXwuZH7aiNSHtsWIwxxs3x9pxPtDb2f0tDnSTZ8ZxAV51do-4dunfE7uvn7ZXn0vbn58u77a3BROKDUXjWqdtZw71QL3DaxbJbnjumZibR2IutWV1HkLzatGg4BWQK1l4ysFPv-tz8nnE-90aPboXdYUbW-mGPY2Hs1og_m7M4TO3I8PRgqVAzLBhyeCOP46YJrNPiSHfW8HHA_JgOKVyKer6v9D60WR4lpnKD9BXRxTitg-KwJmFifNzixOmsVJwyqTncxD7__c5Xnkt3UZ8OkEwHzRh4DRJBdwcOhDRDcbP4Z_8T8Cb5utew</recordid><startdate>20160617</startdate><enddate>20160617</enddate><creator>LeNoue-Newton, Michele L.</creator><creator>Wadzinski, Brian E.</creator><creator>Spiller, Benjamin W.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20160617</creationdate><title>The three Type 2A protein phosphatases, PP2Ac, PP4c and PP6c, are differentially regulated by Alpha4</title><author>LeNoue-Newton, Michele L. ; Wadzinski, Brian E. ; Spiller, Benjamin W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-b8fcaa22c8f12db13f862c297043ac147f9569001925b9141f41796bd581d9253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adaptor Proteins, Signal Transducing</topic><topic>alleles</topic><topic>Alpha4</topic><topic>Catalytic Domain</topic><topic>Gene Knockdown Techniques</topic><topic>HEK293 Cells</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Intracellular Signaling Peptides and Proteins - analysis</topic><topic>Intracellular Signaling Peptides and Proteins - genetics</topic><topic>Intracellular Signaling Peptides and Proteins - metabolism</topic><topic>Lentiviral expression</topic><topic>Molecular Chaperones</topic><topic>mutants</topic><topic>neoplasms</topic><topic>phenotype</topic><topic>Phosphoprotein Phosphatases - analysis</topic><topic>Phosphoprotein Phosphatases - metabolism</topic><topic>Protein Phosphatase 2 - analysis</topic><topic>Protein Phosphatase 2 - metabolism</topic><topic>Protein phosphatase 2A (PP2A)</topic><topic>Protein phosphatases</topic><topic>protein subunits</topic><topic>rapid methods</topic><topic>tissue culture</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LeNoue-Newton, Michele L.</creatorcontrib><creatorcontrib>Wadzinski, Brian E.</creatorcontrib><creatorcontrib>Spiller, Benjamin W.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LeNoue-Newton, Michele L.</au><au>Wadzinski, Brian E.</au><au>Spiller, Benjamin W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The three Type 2A protein phosphatases, PP2Ac, PP4c and PP6c, are differentially regulated by Alpha4</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2016-06-17</date><risdate>2016</risdate><volume>475</volume><issue>1</issue><spage>64</spage><epage>69</epage><pages>64-69</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Alpha4 is a non-canonical regulatory subunit of Type 2A protein phosphatases that interacts directly with the phosphatase catalytic subunits (PP2Ac, PP4c, and PP6c) and is upregulated in a variety of cancers. Alpha4 modulates phosphatase expression levels and activity, but the molecular mechanism of this regulation is unclear, and the extent to which the various Type 2A catalytic subunits associate with Alpha4 is also unknown. To determine the relative fractions of the Type 2A catalytic subunits associated with Alpha4, we conducted Alpha4 immunodepletion experiments in HEK293T cells and found that a significant fraction of total PP6c is associated with Alpha4, whereas a minimal fraction of total PP2Ac is associated with Alpha4. To facilitate studies of phosphatases in the presence of mutant or null Alpha4 alleles, we developed a facile and rapid method to simultaneously knockdown and rescue Alpha4 in tissue culture cells. This approach has the advantage that levels of endogenous Alpha4 are dramatically reduced by shRNA expression thereby simplifying interpretation of mutant phenotypes. 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subjects | Adaptor Proteins, Signal Transducing alleles Alpha4 Catalytic Domain Gene Knockdown Techniques HEK293 Cells HeLa Cells Humans Intracellular Signaling Peptides and Proteins - analysis Intracellular Signaling Peptides and Proteins - genetics Intracellular Signaling Peptides and Proteins - metabolism Lentiviral expression Molecular Chaperones mutants neoplasms phenotype Phosphoprotein Phosphatases - analysis Phosphoprotein Phosphatases - metabolism Protein Phosphatase 2 - analysis Protein Phosphatase 2 - metabolism Protein phosphatase 2A (PP2A) Protein phosphatases protein subunits rapid methods tissue culture |
title | The three Type 2A protein phosphatases, PP2Ac, PP4c and PP6c, are differentially regulated by Alpha4 |
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