Identification of genetic and chemical modulators of zebrafish mechanosensory hair cell death

被引:160
作者
Owens, Kelly N. [1 ,2 ,3 ]
Santos, Felipe [2 ,3 ]
Roberts, Brock [1 ]
Linbo, Tor [1 ]
Coffin, Allison B. [2 ,3 ]
Knisely, Anna J. [2 ,3 ]
Simon, Julian A. [4 ]
Rubel, Edwin W. [2 ,3 ,5 ]
Raible, David W. [1 ,2 ]
机构
[1] Univ Washington, Dept Biol Struct, Seattle, WA 98195 USA
[2] Univ Washington, Virginia Merrill Bloedel Hearing Res Ctr, Seattle, WA 98195 USA
[3] Univ Washington, Dept Otorhinolaryngol Head & Neck Surg, Seattle, WA 98195 USA
[4] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[5] Univ Washington, Dept Physiol & Biophys, Seattle, WA 98195 USA
关键词
D O I
10.1371/journal.pgen.1000020
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Inner ear sensory hair cell death is observed in the majority of hearing and balance disorders, affecting the health of more than 600 million people worldwide. While normal aging is the single greatest contributor, exposure to environmental toxins and therapeutic drugs such as aminoglycoside antibiotics and antineoplastic agents are significant contributors. Genetic variation contributes markedly to differences in normal disease progression during aging and in susceptibility to ototoxic agents. Using the lateral line system of larval zebrafish, we developed an in vivo drug toxicity interaction screen to uncover genetic modulators of antibiotic-induced hair cell death and to identify compounds that confer protection. We have identified 5 mutations that modulate aminoglycoside susceptibility. Further characterization and identification of one protective mutant, sentinel (snl), revealed a novel conserved vertebrate gene. A similar screen identified a new class of drug-like small molecules, benzothiophene carboxamides, that prevent aminoglycoside-induced hair cell death in zebrafish and in mammals. Testing for interaction with the sentinel mutation suggests that the gene and compounds may operate in different pathways. The combination of chemical screening with traditional genetic approaches is a new strategy for identifying drugs and drug targets to attenuate hearing and balance disorders.
引用
收藏
页数:14
相关论文
共 60 条
[1]  
[Anonymous], 1989, Cladistics, DOI DOI 10.1111/J.1096-0031.1989.TB00562.X
[2]   Decoding cilia function: Defining specialized genes required for compartmentalized cilia biogenesis [J].
Avidor-Reiss, T ;
Maer, AM ;
Koundakjian, E ;
Polyanovsky, A ;
Keil, T ;
Subramaniam, S ;
Zuker, CS .
CELL, 2004, 117 (04) :527-539
[3]  
BALAK KJ, 1990, J NEUROSCI, V10, P2502
[4]   DIMETHYLAMINOSTYRYLMETHYLPYRIDINIUMIODINE (DASPMI) AS A FLUORESCENT-PROBE FOR MITOCHONDRIA INSITU [J].
BEREITERHAHN, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 423 (01) :1-14
[5]   Functional genomics of the cilium, a sensory organelle [J].
Blacque, OE ;
Perens, EA ;
Boroevich, KA ;
Inglis, PN ;
Li, CM ;
Warner, A ;
Khattra, J ;
Holt, RA ;
Ou, GS ;
Mah, AK ;
McKay, SJ ;
Huang, P ;
Swoboda, P ;
Jones, SJM ;
Marra, MA ;
Baillie, DL ;
Moerman, DG ;
Shaham, S ;
Leroux, MR .
CURRENT BIOLOGY, 2005, 15 (10) :935-941
[6]   Hair cell death in the avian basilar papilla:: Characterization of the in vitro model and caspase activation [J].
Cheng, AG ;
Cunningham, LL ;
Rubel, EW .
JARO, 2003, 4 (01) :91-105
[7]   Multiple sequence alignment with the Clustal series of programs [J].
Chenna, R ;
Sugawara, H ;
Koike, T ;
Lopez, R ;
Gibson, TJ ;
Higgins, DG ;
Thompson, JD .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3497-3500
[8]   Casein kinase II is a selective target of HIV-1 transcriptional inhibitors [J].
Critchfield, JW ;
Coligan, JE ;
Folks, TM ;
Butera, ST .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (12) :6110-6115
[9]   Overexpression of Bcl-2 prevents neomycin-induced hair cell death and caspase-9 activation in the adult mouse utricle In vitro [J].
Cunningham, LL ;
Matsui, JI ;
Warchol, ME ;
Rubel, EW .
JOURNAL OF NEUROBIOLOGY, 2004, 60 (01) :89-100
[10]  
Cunningham LL, 2002, J NEUROSCI, V22, P8532