Genetically targeted cell disruption in Caenorhabditis elegans

被引:54
作者
Harbinder, S
Tavernarakis, N
Herndon, LA
Kinnell, M
Xu, SQ
Fire, A
Driscoll, M
机构
[1] RUTGERS STATE UNIV,CTR ADV BIOTECHNOL & MED,DEPT MOL BIOL & BIOCHEM,PISCATAWAY,NJ 08855
[2] CARNEGIE INST WASHINGTON,DEPT EMBRYOL,BALTIMORE,MD 21210
关键词
cell death; degenerin; ENaC superfamily; ion channels; cell ablation;
D O I
10.1073/pnas.94.24.13128
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
The elimination of identified cells is a powerful tool for investigating development and system function. Here we report on genetically mediated cell disruption effected by the toxic Caenorhabditis elegans mec-4(d) allele, We found that ectopic expression of mec-4(d) in the nematode causes dysfunction of a wide range of nerve, muscle, and hypodermal cells, mec-4(d)-mediated toxicity is dependent on the activity of a second gene, mec-6, rendering cell disruption conditionally dependent on genetic background. We describe a set of mec-4(d) vectors that facilitate construction of cell-specific disruption reagents and note that genetic cell disruption can be used for functional analyses of specific neurons or neuronal classes, for confirmation of neuronal circuitry, for generation of nematode populations lacking defined classes of functional cells, and for genetic screens. We suggest that mec-4(d) and/or related genes may be effective general tools for cell inactivation that could be used toward similar purposes in higher organisms.
引用
收藏
页码:13128 / 13133
页数:6
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