AF6/s-afadin is a dual residency protein and localizes to a novel subnuclear compartment
The AF6/afadin protein is a component of cell membranes at specialized sites of cell–cell contact. Two main splice variants exist, known as l‐ and s‐afadin, respectively. L‐afadin is widely expressed in cells of epithelial origin, whilst s‐afadin expression is restricted to the brain. Here we demons...
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Veröffentlicht in: | Journal of cellular physiology 2007-01, Vol.210 (1), p.212-223 |
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description | The AF6/afadin protein is a component of cell membranes at specialized sites of cell–cell contact. Two main splice variants exist, known as l‐ and s‐afadin, respectively. L‐afadin is widely expressed in cells of epithelial origin, whilst s‐afadin expression is restricted to the brain. Here we demonstrate that the short form of AF6/s‐afadin is a dual residency protein able to localize to the plasma membrane or nucleus whilst the long form of AF6, l‐afadin is unable to localize to the nucleus. AF6/s‐afadin clusters in a distinctive speckled pattern in the nucleus, but is unable to do so when cell cycle progression is inhibited at the G1/S or G2/M checkpoints. The formation of AF6/s‐afadin nuclear bodies is also sensitive to the transcriptional activity of the cell with inhibition of RNA polymerase activity abolishing AF6/s‐afadin nuclear clustering. AF6/s‐afadin nuclear bodies localize to a novel subnuclear compartment, failing to colocalize with other known nuclear bodies. Formation of the AF6/s‐afadin nuclear foci can be regulated by specific growth factor receptor mediated signaling events and by cytoplasmic tyrosine kinases, but does not correlate with tyrosine phosphorylation of AF6/s‐afadin. AF6/s‐afadin is a candidate for mediating control of cellular growth processes by regulated translocation to the nucleus. J. Cell. Physiol. 210: 212–223, 2007. © 2006 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/jcp.20853 |
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Two main splice variants exist, known as l‐ and s‐afadin, respectively. L‐afadin is widely expressed in cells of epithelial origin, whilst s‐afadin expression is restricted to the brain. Here we demonstrate that the short form of AF6/s‐afadin is a dual residency protein able to localize to the plasma membrane or nucleus whilst the long form of AF6, l‐afadin is unable to localize to the nucleus. AF6/s‐afadin clusters in a distinctive speckled pattern in the nucleus, but is unable to do so when cell cycle progression is inhibited at the G1/S or G2/M checkpoints. The formation of AF6/s‐afadin nuclear bodies is also sensitive to the transcriptional activity of the cell with inhibition of RNA polymerase activity abolishing AF6/s‐afadin nuclear clustering. AF6/s‐afadin nuclear bodies localize to a novel subnuclear compartment, failing to colocalize with other known nuclear bodies. Formation of the AF6/s‐afadin nuclear foci can be regulated by specific growth factor receptor mediated signaling events and by cytoplasmic tyrosine kinases, but does not correlate with tyrosine phosphorylation of AF6/s‐afadin. AF6/s‐afadin is a candidate for mediating control of cellular growth processes by regulated translocation to the nucleus. J. Cell. Physiol. 210: 212–223, 2007. © 2006 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.20853</identifier><identifier>PMID: 17013812</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Alternative Splicing ; Animals ; Cell Cycle - drug effects ; Cell Line ; Cell Membrane - metabolism ; Cell Nucleus - metabolism ; Cell Nucleus Structures - metabolism ; DNA-Directed RNA Polymerases - antagonists & inhibitors ; Dogs ; Green Fluorescent Proteins - genetics ; Humans ; Kinesin - genetics ; Kinesin - metabolism ; LIM Domain Proteins ; Microfilament Proteins - genetics ; Microfilament Proteins - metabolism ; Mitosis Modulators - pharmacology ; Myosins - genetics ; Myosins - metabolism ; Nucleic Acid Synthesis Inhibitors - pharmacology ; Oligopeptides ; Peptides - genetics ; Phosphorylation ; Protein Transport - drug effects ; Protein-Tyrosine Kinases - genetics ; Protein-Tyrosine Kinases - metabolism ; Rats ; Recombinant Proteins - metabolism ; Signal Transduction ; Time Factors ; Transcription, Genetic - drug effects ; Transfection</subject><ispartof>Journal of cellular physiology, 2007-01, Vol.210 (1), p.212-223</ispartof><rights>Copyright © 2006 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3613-712fad8dd31028f16d703c040688168f56cfa0a76ed11e19be818d5264f3f3e63</citedby><cites>FETCH-LOGICAL-c3613-712fad8dd31028f16d703c040688168f56cfa0a76ed11e19be818d5264f3f3e63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjcp.20853$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcp.20853$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17013812$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Buchert, Michael</creatorcontrib><creatorcontrib>Poon, Carole</creatorcontrib><creatorcontrib>King, James A.J.</creatorcontrib><creatorcontrib>Baechi, Thomas</creatorcontrib><creatorcontrib>D'Abaco, Giovanna</creatorcontrib><creatorcontrib>Hollande, Frédéric</creatorcontrib><creatorcontrib>Hovens, Christopher M.</creatorcontrib><title>AF6/s-afadin is a dual residency protein and localizes to a novel subnuclear compartment</title><title>Journal of cellular physiology</title><addtitle>J. Cell. Physiol</addtitle><description>The AF6/afadin protein is a component of cell membranes at specialized sites of cell–cell contact. Two main splice variants exist, known as l‐ and s‐afadin, respectively. L‐afadin is widely expressed in cells of epithelial origin, whilst s‐afadin expression is restricted to the brain. Here we demonstrate that the short form of AF6/s‐afadin is a dual residency protein able to localize to the plasma membrane or nucleus whilst the long form of AF6, l‐afadin is unable to localize to the nucleus. AF6/s‐afadin clusters in a distinctive speckled pattern in the nucleus, but is unable to do so when cell cycle progression is inhibited at the G1/S or G2/M checkpoints. The formation of AF6/s‐afadin nuclear bodies is also sensitive to the transcriptional activity of the cell with inhibition of RNA polymerase activity abolishing AF6/s‐afadin nuclear clustering. AF6/s‐afadin nuclear bodies localize to a novel subnuclear compartment, failing to colocalize with other known nuclear bodies. Formation of the AF6/s‐afadin nuclear foci can be regulated by specific growth factor receptor mediated signaling events and by cytoplasmic tyrosine kinases, but does not correlate with tyrosine phosphorylation of AF6/s‐afadin. AF6/s‐afadin is a candidate for mediating control of cellular growth processes by regulated translocation to the nucleus. J. Cell. Physiol. 210: 212–223, 2007. © 2006 Wiley‐Liss, Inc.</description><subject>Alternative Splicing</subject><subject>Animals</subject><subject>Cell Cycle - drug effects</subject><subject>Cell Line</subject><subject>Cell Membrane - metabolism</subject><subject>Cell Nucleus - metabolism</subject><subject>Cell Nucleus Structures - metabolism</subject><subject>DNA-Directed RNA Polymerases - antagonists & inhibitors</subject><subject>Dogs</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Humans</subject><subject>Kinesin - genetics</subject><subject>Kinesin - metabolism</subject><subject>LIM Domain Proteins</subject><subject>Microfilament Proteins - genetics</subject><subject>Microfilament Proteins - metabolism</subject><subject>Mitosis Modulators - pharmacology</subject><subject>Myosins - genetics</subject><subject>Myosins - metabolism</subject><subject>Nucleic Acid Synthesis Inhibitors - pharmacology</subject><subject>Oligopeptides</subject><subject>Peptides - genetics</subject><subject>Phosphorylation</subject><subject>Protein Transport - drug effects</subject><subject>Protein-Tyrosine Kinases - genetics</subject><subject>Protein-Tyrosine Kinases - metabolism</subject><subject>Rats</subject><subject>Recombinant Proteins - metabolism</subject><subject>Signal Transduction</subject><subject>Time Factors</subject><subject>Transcription, Genetic - drug effects</subject><subject>Transfection</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1P3DAQhq0K1F0-Dv0DlU9IHMJ64sRxjqtVgQJaEAKBerG89kTK4iRbO6Hd_noMu4UTpznM8z4zegn5BuwEGEsnS7M6SZnM-RcyBlYWSSbydIeM4w6SMs9gRPZCWDLGypLzr2QEBQMuIR2Tx-mpmIREV9rWLa0D1dQO2lGPobbYmjVd-a7HuNOtpa4z2tX_MNC-i2TbPaOjYVi0g3GoPTVds9K-b7DtD8hupV3Aw-3cJ_enP-5m58nV9dnP2fQqMVwATwpI42lpLQeWygqELRg3LGNCShCyyoWpNNOFQAuAUC5QgrR5KrKKVxwF3ydHG2_88_eAoVdNHQw6p1vshqCE5CJjaRHB4w1ofBeCx0qtfN1ov1bA1GuNKtao3mqM7PetdFg0aD_IbW8RmGyAP7XD9ecmdTG7-a9MNok69Pj3PaH9kxIFL3L1MD9T87uL28e8vFS_-AtE94qg</recordid><startdate>200701</startdate><enddate>200701</enddate><creator>Buchert, Michael</creator><creator>Poon, Carole</creator><creator>King, James A.J.</creator><creator>Baechi, Thomas</creator><creator>D'Abaco, Giovanna</creator><creator>Hollande, Frédéric</creator><creator>Hovens, Christopher M.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><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></search><sort><creationdate>200701</creationdate><title>AF6/s-afadin is a dual residency protein and localizes to a novel subnuclear compartment</title><author>Buchert, Michael ; Poon, Carole ; King, James A.J. ; Baechi, Thomas ; D'Abaco, Giovanna ; Hollande, Frédéric ; Hovens, Christopher M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3613-712fad8dd31028f16d703c040688168f56cfa0a76ed11e19be818d5264f3f3e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Alternative Splicing</topic><topic>Animals</topic><topic>Cell Cycle - drug effects</topic><topic>Cell Line</topic><topic>Cell Membrane - metabolism</topic><topic>Cell Nucleus - metabolism</topic><topic>Cell Nucleus Structures - metabolism</topic><topic>DNA-Directed RNA Polymerases - antagonists & inhibitors</topic><topic>Dogs</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Humans</topic><topic>Kinesin - genetics</topic><topic>Kinesin - metabolism</topic><topic>LIM Domain Proteins</topic><topic>Microfilament Proteins - genetics</topic><topic>Microfilament Proteins - metabolism</topic><topic>Mitosis Modulators - pharmacology</topic><topic>Myosins - genetics</topic><topic>Myosins - metabolism</topic><topic>Nucleic Acid Synthesis Inhibitors - pharmacology</topic><topic>Oligopeptides</topic><topic>Peptides - genetics</topic><topic>Phosphorylation</topic><topic>Protein Transport - drug effects</topic><topic>Protein-Tyrosine Kinases - genetics</topic><topic>Protein-Tyrosine Kinases - metabolism</topic><topic>Rats</topic><topic>Recombinant Proteins - metabolism</topic><topic>Signal Transduction</topic><topic>Time Factors</topic><topic>Transcription, Genetic - drug effects</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Buchert, Michael</creatorcontrib><creatorcontrib>Poon, Carole</creatorcontrib><creatorcontrib>King, James A.J.</creatorcontrib><creatorcontrib>Baechi, Thomas</creatorcontrib><creatorcontrib>D'Abaco, Giovanna</creatorcontrib><creatorcontrib>Hollande, Frédéric</creatorcontrib><creatorcontrib>Hovens, Christopher M.</creatorcontrib><collection>Istex</collection><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><jtitle>Journal of cellular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Buchert, Michael</au><au>Poon, Carole</au><au>King, James A.J.</au><au>Baechi, Thomas</au><au>D'Abaco, Giovanna</au><au>Hollande, Frédéric</au><au>Hovens, Christopher M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>AF6/s-afadin is a dual residency protein and localizes to a novel subnuclear compartment</atitle><jtitle>Journal of cellular physiology</jtitle><addtitle>J. Cell. Physiol</addtitle><date>2007-01</date><risdate>2007</risdate><volume>210</volume><issue>1</issue><spage>212</spage><epage>223</epage><pages>212-223</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><abstract>The AF6/afadin protein is a component of cell membranes at specialized sites of cell–cell contact. Two main splice variants exist, known as l‐ and s‐afadin, respectively. L‐afadin is widely expressed in cells of epithelial origin, whilst s‐afadin expression is restricted to the brain. Here we demonstrate that the short form of AF6/s‐afadin is a dual residency protein able to localize to the plasma membrane or nucleus whilst the long form of AF6, l‐afadin is unable to localize to the nucleus. AF6/s‐afadin clusters in a distinctive speckled pattern in the nucleus, but is unable to do so when cell cycle progression is inhibited at the G1/S or G2/M checkpoints. The formation of AF6/s‐afadin nuclear bodies is also sensitive to the transcriptional activity of the cell with inhibition of RNA polymerase activity abolishing AF6/s‐afadin nuclear clustering. AF6/s‐afadin nuclear bodies localize to a novel subnuclear compartment, failing to colocalize with other known nuclear bodies. Formation of the AF6/s‐afadin nuclear foci can be regulated by specific growth factor receptor mediated signaling events and by cytoplasmic tyrosine kinases, but does not correlate with tyrosine phosphorylation of AF6/s‐afadin. AF6/s‐afadin is a candidate for mediating control of cellular growth processes by regulated translocation to the nucleus. J. Cell. Physiol. 210: 212–223, 2007. © 2006 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17013812</pmid><doi>10.1002/jcp.20853</doi><tpages>12</tpages></addata></record> |
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subjects | Alternative Splicing Animals Cell Cycle - drug effects Cell Line Cell Membrane - metabolism Cell Nucleus - metabolism Cell Nucleus Structures - metabolism DNA-Directed RNA Polymerases - antagonists & inhibitors Dogs Green Fluorescent Proteins - genetics Humans Kinesin - genetics Kinesin - metabolism LIM Domain Proteins Microfilament Proteins - genetics Microfilament Proteins - metabolism Mitosis Modulators - pharmacology Myosins - genetics Myosins - metabolism Nucleic Acid Synthesis Inhibitors - pharmacology Oligopeptides Peptides - genetics Phosphorylation Protein Transport - drug effects Protein-Tyrosine Kinases - genetics Protein-Tyrosine Kinases - metabolism Rats Recombinant Proteins - metabolism Signal Transduction Time Factors Transcription, Genetic - drug effects Transfection |
title | AF6/s-afadin is a dual residency protein and localizes to a novel subnuclear compartment |
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