Mechanisms of Ephrin Receptor Protein Kinase-Independent Signaling in Amphid Axon Guidance in Caenorhabditis elegans

被引:16
作者
Grossman, Emily N. [1 ]
Giurumescu, Claudiu A. [1 ]
Chisholm, Andrew D. [1 ]
机构
[1] Univ Calif San Diego, Sect Cell & Dev Biol, Div Biol Sci, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
Ephrin; amphid; left-right asymmetry; Abl tyrosine kinase; phosphatidylinositol; 3-kinase; OOCYTE MEIOTIC MATURATION; AGE-1; PI3; KINASE; TYROSINE KINASE; CHEMOSENSORY NEURONS; LEFT/RIGHT ASYMMETRY; DEPENDENT INDUCTION; REGULATORY CASCADE; SENSORY NEURONS; FAMILY KINASES; CELL LINEAGE;
D O I
10.1534/genetics.113.154393
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Eph receptors and their ephrin ligands are key conserved regulators of axon guidance and can function in a variety of signaling modes. Here we analyze the genetic and cellular requirements for Eph signaling in a Caenorhabditis elegans axon guidance choice point, the ventral guidance of axons in the amphid commissure. The C. elegans Eph receptor EFN-1 has both kinase-dependent and kinase-independent roles in amphid ventral guidance. Of the four C. elegans ephrins, we find that only EFN-1 has a major role in amphid axon ventral guidance, and signals in both a receptor kinase-dependent and kinase-independent manner. Analysis of EFN-1 and EFN-1 expression and tissue-specific requirements is consistent with a model in which VAB-1 acts in amphid neurons, interacting with EFN-1 expressed on surrounding cells. Unexpectedly, left-hand neurons are more strongly affected than right-hand neurons by loss of Eph signaling, indicating a previously undetected left-right asymmetry in the requirement for Eph signaling. By screening candidate genes involved in Eph signaling, we find that the Eph kinase-independent pathway involves the ABL-1 nonreceptor tyrosine kinase and possibly the phosphatidylinositol 3-kinase pathway. Overexpression of ABL-1 is sufficient to rescue EFN-1 ventral guidance defects cell autonomously. Our results reveal new aspects of Eph signaling in a single axon guidance decision in vivo.
引用
收藏
页码:899 / +
页数:19
相关论文
共 81 条
[1]   UNC-6/Netrin induces neuronal asymmetry and defines the site of axon formation [J].
Adler, CE ;
Fetter, RD ;
Bargmann, CI .
NATURE NEUROSCIENCE, 2006, 9 (04) :511-518
[2]  
Altun-Gultekin Z, 2001, DEVELOPMENT, V128, P1951
[3]   CHEMOSENSORY NEURONS WITH OVERLAPPING FUNCTIONS DIRECT CHEMOTAXIS TO MULTIPLE CHEMICALS IN C-ELEGANS [J].
BARGMANN, CI ;
HORVITZ, HR .
NEURON, 1991, 7 (05) :729-742
[4]   Notch-Dependent Induction of Left/Right Asymmetry in C. elegans Interneurons and Motoneurons [J].
Bertrand, Vincent ;
Bisso, Paul ;
Poole, Richard J. ;
Hobert, Oliver .
CURRENT BIOLOGY, 2011, 21 (14) :1225-1231
[5]   Ret Is a Multifunctional Coreceptor that Integrates Diffusible- and Contact-Axon Guidance Signals [J].
Bonanomi, Dario ;
Chivatakarn, Onanong ;
Bai, Ge ;
Abdesselem, Houari ;
Lettieri, Karen ;
Marquardt, Till ;
Pierchala, Brian A. ;
Pfaff, Samuel L. .
CELL, 2012, 148 (03) :568-582
[6]   A novel Eph receptor-interacting IgSF protein provides C. elegans motoneurons with midline guidepost function [J].
Boulin, Thomas ;
Pocock, Roger ;
Hobert, Oliver .
CURRENT BIOLOGY, 2006, 16 (19) :1871-1883
[7]   A Role for C. elegans Eph RTK Signaling in PTEN Regulation [J].
Brisbin, Sarah ;
Liu, Jun ;
Boudreau, Jeff ;
Peng, Jimmy ;
Evangelista, Marie ;
Chin-Sang, Ian .
DEVELOPMENTAL CELL, 2009, 17 (04) :459-469
[8]   EphrinB ligands recruit GRIP family PDZ adaptor proteins into raft membrane microdomains [J].
Brückner, K ;
Labrador, JP ;
Scheiffele, P ;
Herb, A ;
Seeburg, PH ;
Klein, R .
NEURON, 1999, 22 (03) :511-524
[9]   Heparan sulfate proteoglycan-dependent induction of axon branching and axon misrouting by the Kallmann syndrome gene kal-1 [J].
Bülow, HE ;
Berry, KL ;
Topper, LH ;
Peles, E ;
Hobert, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (09) :6346-6351
[10]   Silencing of EphA3 through a cis interaction with ephrinA5 [J].
Carvalho, RF ;
Beutler, M ;
Marler, KJM ;
Knöll, B ;
Becker-Barroso, E ;
Heintzmann, R ;
Ng, T ;
Drescher, U .
NATURE NEUROSCIENCE, 2006, 9 (03) :322-330