short stop is allelic to kakapo, and encodes rod-like cytoskeletal-associated proteins required for axon extension

被引:89
作者
Lee, S
Harris, KL
Whitington, PM
Kolodziej, PA
机构
[1] Vanderbilt Univ, Med Ctr, Dept Cell Biol, Ctr Mol Neurosci, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Med Ctr, Howard Hughes Med Inst, Nashville, TN 37232 USA
[3] Univ New England, Sch Biol Sci, Armidale, NSW 2351, Australia
关键词
Drosophila; cytoskeleton; GAS2; axon; growth cone; short stop; kakapo;
D O I
10.1523/JNEUROSCI.20-03-01096.2000
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
short stop (shot) is required for sensory and motor axons to reach their targets in the Drosophila embryo. Growth cones in shot mutants initiate at the normal times, and they appear normal with respect to overall morphology and their abilities to orient and fasciculate. However, sensory axons are unable to extend beyond a short distance from the cell body, and motor axons are unable to reach target muscles. The shot gene encodes novel actin binding proteins that are related to plakins and dystrophin and expressed in axons during development. The longer isoforms identified are predicted to contain an N-terminal actin binding domain, a long central triple helical coiled-coil domain, and a C-terminal domain that contains two EF-hand Ca2+ binding motifs and a short stretch of homology to the growth arrest-specific 2 protein. Other isoforms lack all or part of the actin binding domains or are truncated and contain a different C-terminal domain. Only the isoforms containing full-length actin binding domains are detectably expressed in the nervous system. shot is allelic to kakapo, a gene that may function in integrin-mediated adhesion in the wing and embryo. We propose that Shot's interactions with the actin cytoskeleton allow sensory and motor axons to extend.
引用
收藏
页码:1096 / 1108
页数:13
相关论文
共 63 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   Not just scaffolding:: plectin regulates actin dynamics in cultured cells [J].
Andrä, K ;
Nikolic, B ;
Stöcher, M ;
Drenckhahn, D ;
Wiche, G .
GENES & DEVELOPMENT, 1998, 12 (21) :3442-3451
[3]   DISORIENTED PATHFINDING BY PIONEER NEURON GROWTH CONES DEPRIVED OF FILOPODIA BY CYTOCHALASIN TREATMENT [J].
BENTLEY, D ;
TOROIANRAYMOND, A .
NATURE, 1986, 323 (6090) :712-715
[4]   Cloning and characterization of mouse ACF7, a novel member of the dystonin subfamily of actin binding proteins [J].
Bernier, G ;
Mathieu, M ;
DeRepentigny, Y ;
Vidal, SM ;
Kothary, R .
GENOMICS, 1996, 38 (01) :19-29
[5]   SEARCHING FOR PATTERN AND MUTATION IN THE DROSOPHILA GENOME WITH A P-LACZ VECTOR [J].
BIER, E ;
VAESSIN, H ;
SHEPHERD, S ;
LEE, K ;
MCCALL, K ;
BARBEL, S ;
ACKERMAN, L ;
CARRETTO, R ;
UEMURA, T ;
GRELL, E ;
JAN, LY ;
JAN, YN .
GENES & DEVELOPMENT, 1989, 3 (09) :1273-1287
[6]   GAS2, A GROWTH ARREST SPECIFIC PROTEIN, IS A COMPONENT OF THE MICROFILAMENT NETWORK SYSTEM [J].
BRANCOLINI, C ;
BOTTEGA, S ;
SCHNEIDER, C .
JOURNAL OF CELL BIOLOGY, 1992, 117 (06) :1251-1261
[7]   PHOSPHORYLATION OF THE GROWTH ARREST-SPECIFIC PROTEIN GAS2 IS COUPLED TO ACTIN REARRANGEMENTS DURING GO-]G1 TRANSITION IN NIH 3T3 CELLS [J].
BRANCOLINI, C ;
SCHNEIDER, C .
JOURNAL OF CELL BIOLOGY, 1994, 124 (05) :743-756
[8]   CLONING AND CHARACTERIZATION OF THE NEURAL ISOFORMS OF HUMAN DYSTONIN [J].
BROWN, A ;
DALPE, G ;
MATHIEU, M ;
KOTHARY, R .
GENOMICS, 1995, 29 (03) :777-780
[9]   THE MOUSE DYSTONIA MUSCULORUM GENE IS A NEURAL ISOFORM OF BULLOUS PEMPHIGOID ANTIGEN-1 [J].
BROWN, A ;
BERNIER, G ;
MATHIEU, M ;
ROSSANT, J ;
KOTHARY, R .
NATURE GENETICS, 1995, 10 (03) :301-306
[10]   FUNCTIONAL CDNA LIBRARIES FROM DROSOPHILA EMBRYOS [J].
BROWN, NH ;
KAFATOS, FC .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 203 (02) :425-437