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
Hauptverfasser: Buchert, Michael, Poon, Carole, King, James A.J., Baechi, Thomas, D'Abaco, Giovanna, Hollande, Frédéric, Hovens, Christopher M.
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container_end_page 223
container_issue 1
container_start_page 212
container_title Journal of cellular physiology
container_volume 210
creator Buchert, Michael
Poon, Carole
King, James A.J.
Baechi, Thomas
D'Abaco, Giovanna
Hollande, Frédéric
Hovens, Christopher M.
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. 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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. 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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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