Synaptic tetraspan vesicle membrane proteins are conserved but not needed for synaptogenesis and neuronal function in Caenorhabditis elegans

被引:27
作者
Abraham, Christian
Hutter, Harald
Palfreyman, Mark T.
Spatkowski, Gabriele
Weimer, Robby M.
Windoffer, Reinhard
Jorgensen, Erik M.
Leube, Rudolf E.
机构
[1] Johannes Gutenberg Univ Mainz, Dept Anat & Cell Biol, D-55128 Mainz, Germany
[2] Max Planck Inst Med Res, D-69120 Heidelberg, Germany
[3] Univ Utah, Dept Biol, Salt Lake City, UT 84112 USA
[4] Univ Utah, Howard Hughes Med Inst, Salt Lake City, UT 84112 USA
[5] Ecole Normale Super, F-75005 Paris, France
关键词
integral membrane proteins; phylogenesis; vesicle trafficking; synaptophysin; synaptogyrin;
D O I
10.1073/pnas.0509400103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tetraspan vesicle membrane proteins (TVPs) comprise a major portion of synaptic vesicle proteins, yet their contribution to the synaptic vesicle cycle is poorly understood. TVPs are grouped in three mammalian gene families: physins, gyrins, and secretory carrier-associated membrane proteins (SCAMPs). In Caenorhabditis elegans, only a single member of each of these families exists. These three nematode TVPs colocalize to the same vesicular compartment when expressed in mammalian cells, suggesting that they could serve overlapping functions. To examine their function, C. eiegans null mutants were isolated for each gene, and a triple mutant was generated. Surprisingly, these animals develop normally and exhibit normal neuronal architecture and synaptic contacts. in addition, functions of the motor and sensory systems are normal as determined by pharmacological, chemotaxis, and thermotaxis assays. Finally, direct electrophysiological analysis of the neuromuscular junction revealed no phenotype in the TVP mutants. We therefore conclude that TVPs are not needed for the basic neuronal machinery and instead may contribute to subtle higher order functions.
引用
收藏
页码:8227 / 8232
页数:6
相关论文
共 34 条
[1]  
Becher A, 1999, J NEUROSCI, V19, P1922
[2]   The synaptophysin-synaptobrevin complex is developmentally upregulated in cultivated neurons but is absent in neuroendocrine cells [J].
Becher, A ;
Drenckhahn, A ;
Pahner, I ;
Ahnert-Hilger, G .
EUROPEAN JOURNAL OF CELL BIOLOGY, 1999, 78 (09) :650-656
[3]   Cellugyrin induces biogenesis of synaptic-like microvesicles in PC12 cells [J].
Belfort, GM ;
Bakirtzi, K ;
Kandror, KV .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (08) :7262-7272
[4]   TRANSSPLICING AND POLYCISTRONIC TRANSCRIPTION IN CAENORHABDITIS-ELEGANS [J].
BLUMENTHAL, T .
TRENDS IN GENETICS, 1995, 11 (04) :132-136
[5]  
CALAKOS N, 1994, J BIOL CHEM, V269, P24534
[6]   A dynamin GTPase mutation causes a rapid and reversible temperature-inducible locomotion defect in C-elegans [J].
Clark, SG ;
Shurland, DL ;
Meyerowitz, EM ;
Bargmann, CI ;
vanderBliek, AM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (19) :10438-10443
[7]   Ca2+-dependent formation of a dynamin-synaptophysin complex -: Potential role in synaptic vesicle endocytosis [J].
Daly, C ;
Ziff, EB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (11) :9010-9015
[8]   Synaptophysin regulates clathrin-independent endocytosis of synaptic vesicles [J].
Daly, C ;
Sugimori, M ;
Moreira, JE ;
Ziff, EB ;
Llinás, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) :6120-6125
[9]   SYNAPTOBREVIN BINDING TO SYNAPTOPHYSIN - A POTENTIAL MECHANISM FOR CONTROLLING THE EXOCYTOTIC FUSION MACHINE [J].
EDELMANN, L ;
HANSON, PI ;
CHAPMAN, ER ;
JAHN, R .
EMBO JOURNAL, 1995, 14 (02) :224-231
[10]   Improved detection of small deletions in complex pools of DNA [J].
Edgley, M ;
D'Souza, A ;
Moulder, G ;
McKay, S ;
Shen, B ;
Gilchrist, E ;
Moerman, D ;
Barstead, R .
NUCLEIC ACIDS RESEARCH, 2002, 30 (12) :e52