The short coiled-coil domain-containing protein UNC-69 cooperates with UNC-76 to regulate axonal outgrowth and normal presynaptic organization in <it>Caenorhabditis elegans</it>

<p>Abstract</p> <p>Background</p> <p>The nematode <it>Caenorhabditis elegans </it>has been used extensively to identify the genetic requirements for proper nervous system development and function. Key to this process is the direction of vesicles to the growi...

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Main Authors: Tsung Nancy, Meili David, Spector Mona, Wightman Bruce, Jin Yishi, Tharin Suzanne, Su Cheng-Wen, Rhiner Christa, Bourikas Dimitris, Stoeckli Esther, Garriga Gian, Horvitz H Robert, Hengartner Michael O
Format: Article
Language:English
Published: BMC 2006-05-01
Series:Journal of Biology
Online Access:http://jbiol.com/content/5/4/9
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author Tsung Nancy
Meili David
Spector Mona
Wightman Bruce
Jin Yishi
Tharin Suzanne
Su Cheng-Wen
Rhiner Christa
Bourikas Dimitris
Stoeckli Esther
Garriga Gian
Horvitz H Robert
Hengartner Michael O
author_facet Tsung Nancy
Meili David
Spector Mona
Wightman Bruce
Jin Yishi
Tharin Suzanne
Su Cheng-Wen
Rhiner Christa
Bourikas Dimitris
Stoeckli Esther
Garriga Gian
Horvitz H Robert
Hengartner Michael O
author_sort Tsung Nancy
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>The nematode <it>Caenorhabditis elegans </it>has been used extensively to identify the genetic requirements for proper nervous system development and function. Key to this process is the direction of vesicles to the growing axons and dendrites, which is required for growth-cone extension and synapse formation in the developing neurons. The contribution and mechanism of membrane traffic in neuronal development are not fully understood, however.</p> <p>Results</p> <p>We show that the <it>C. elegans </it>gene <it>unc-69 </it>is required for axon outgrowth, guidance, fasciculation and normal presynaptic organization. We identify UNC-69 as an evolutionarily conserved 108-amino-acid protein with a short coiled-coil domain. UNC-69 interacts physically with UNC-76, mutations in which produce similar defects to loss of <it>unc-69 </it>function. In addition, a weak reduction-of-function allele, <it>unc-69(ju69)</it>, preferentially causes mislocalization of the synaptic vesicle marker synaptobrevin. UNC-69 and UNC-76 colocalize as puncta in neuronal processes and cooperate to regulate axon extension and synapse formation. The chicken UNC-69 homolog is highly expressed in the developing central nervous system, and its inactivation by RNA interference leads to axon guidance defects.</p> <p>Conclusion</p> <p>We have identified a novel protein complex, composed of UNC-69 and UNC-76, which promotes axonal growth and normal presynaptic organization in <it>C. elegans</it>. As both proteins are conserved through evolution, we suggest that the mammalian homologs of UNC-69 and UNC-76 (SCOCO and FEZ, respectively) may function similarly.</p>
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spelling doaj.art-b9813b1cbde245529832bce58e02f4c82022-12-22T02:01:09ZengBMCJournal of Biology1478-58541475-49242006-05-0154910.1186/jbiol39The short coiled-coil domain-containing protein UNC-69 cooperates with UNC-76 to regulate axonal outgrowth and normal presynaptic organization in <it>Caenorhabditis elegans</it>Tsung NancyMeili DavidSpector MonaWightman BruceJin YishiTharin SuzanneSu Cheng-WenRhiner ChristaBourikas DimitrisStoeckli EstherGarriga GianHorvitz H RobertHengartner Michael O<p>Abstract</p> <p>Background</p> <p>The nematode <it>Caenorhabditis elegans </it>has been used extensively to identify the genetic requirements for proper nervous system development and function. Key to this process is the direction of vesicles to the growing axons and dendrites, which is required for growth-cone extension and synapse formation in the developing neurons. The contribution and mechanism of membrane traffic in neuronal development are not fully understood, however.</p> <p>Results</p> <p>We show that the <it>C. elegans </it>gene <it>unc-69 </it>is required for axon outgrowth, guidance, fasciculation and normal presynaptic organization. We identify UNC-69 as an evolutionarily conserved 108-amino-acid protein with a short coiled-coil domain. UNC-69 interacts physically with UNC-76, mutations in which produce similar defects to loss of <it>unc-69 </it>function. In addition, a weak reduction-of-function allele, <it>unc-69(ju69)</it>, preferentially causes mislocalization of the synaptic vesicle marker synaptobrevin. UNC-69 and UNC-76 colocalize as puncta in neuronal processes and cooperate to regulate axon extension and synapse formation. The chicken UNC-69 homolog is highly expressed in the developing central nervous system, and its inactivation by RNA interference leads to axon guidance defects.</p> <p>Conclusion</p> <p>We have identified a novel protein complex, composed of UNC-69 and UNC-76, which promotes axonal growth and normal presynaptic organization in <it>C. elegans</it>. As both proteins are conserved through evolution, we suggest that the mammalian homologs of UNC-69 and UNC-76 (SCOCO and FEZ, respectively) may function similarly.</p>http://jbiol.com/content/5/4/9
spellingShingle Tsung Nancy
Meili David
Spector Mona
Wightman Bruce
Jin Yishi
Tharin Suzanne
Su Cheng-Wen
Rhiner Christa
Bourikas Dimitris
Stoeckli Esther
Garriga Gian
Horvitz H Robert
Hengartner Michael O
The short coiled-coil domain-containing protein UNC-69 cooperates with UNC-76 to regulate axonal outgrowth and normal presynaptic organization in <it>Caenorhabditis elegans</it>
Journal of Biology
title The short coiled-coil domain-containing protein UNC-69 cooperates with UNC-76 to regulate axonal outgrowth and normal presynaptic organization in <it>Caenorhabditis elegans</it>
title_full The short coiled-coil domain-containing protein UNC-69 cooperates with UNC-76 to regulate axonal outgrowth and normal presynaptic organization in <it>Caenorhabditis elegans</it>
title_fullStr The short coiled-coil domain-containing protein UNC-69 cooperates with UNC-76 to regulate axonal outgrowth and normal presynaptic organization in <it>Caenorhabditis elegans</it>
title_full_unstemmed The short coiled-coil domain-containing protein UNC-69 cooperates with UNC-76 to regulate axonal outgrowth and normal presynaptic organization in <it>Caenorhabditis elegans</it>
title_short The short coiled-coil domain-containing protein UNC-69 cooperates with UNC-76 to regulate axonal outgrowth and normal presynaptic organization in <it>Caenorhabditis elegans</it>
title_sort short coiled coil domain containing protein unc 69 cooperates with unc 76 to regulate axonal outgrowth and normal presynaptic organization in it caenorhabditis elegans it
url http://jbiol.com/content/5/4/9
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