Mutation of the zebrafish choroideremia gene encoding Rab escort protein 1 devastates hair cells.

To identify genes important for hair-cell function, we conducted a mutagenic screen in zebrafish. Larvae from one mutant line, ru848, were unresponsive to acoustic stimuli and unable to balance. The mutation results in a 90% reduction in hair-cell number and partial retinal degeneration by 5 days postfertilization. We localized the recessive ru848 mutation by positional cloning to the zebrafish homolog of the human Choroideremia gene, which encodes Rab escort protein 1. This protein is essential for the normal prenylation of Rabs. Mutations in the human gene induce choroideremia, a disease marked by slow-onset degeneration of rod photoreceptors and retinal pigment epithelial cells. The degenerative phenotype resulting from a null mutation in the zebrafish gene indicates that hair cells and retinal cells require Rab escort protein 1 for survival.

[1]  J. Pereira-Leal,et al.  Evolution of the Rab family of small GTP-binding proteins. , 2001, Journal of molecular biology.

[2]  A. Ghysen,et al.  Pattern formation in the lateral line of zebrafish , 2001, Mechanisms of Development.

[3]  Marino Zerial,et al.  Rab proteins as membrane organizers , 2001, Nature Reviews Molecular Cell Biology.

[4]  Richard O. Hynes,et al.  The Evolution of Cell Adhesion , 2000, The Journal of cell biology.

[5]  W. Balch,et al.  Molecular Basis for Rab Prenylation , 2000, The Journal of cell biology.

[6]  D. Raible,et al.  Organization of the lateral line system in embryonic zebrafish , 2000, The Journal of comparative neurology.

[7]  C. Zuker,et al.  A Drosophila mechanosensory transduction channel. , 2000, Science.

[8]  E. Knapik,et al.  Zebrafish genetic map with 2000 microsatellite markers. , 1999, Genomics.

[9]  S. Ekker,et al.  Vectors and techniques for ectopic gene expression in zebrafish. , 1999, Methods in cell biology.

[10]  Alexander F. Schier,et al.  Positional Cloning Identifies Zebrafish one-eyed pinhead as a Permissive EGF-Related Ligand Required during Gastrulation , 1998, Cell.

[11]  C. Janetopoulos,et al.  A critical period of ear development controlled by distinct populations of ciliated cells in the zebrafish. , 1997, Developmental biology.

[12]  E. Zrenner,et al.  Mouse choroideremia gene mutation causes photoreceptor cell degeneration and is not transmitted through the female germline. , 1997, Human molecular genetics.

[13]  D A Kane,et al.  The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio. , 1996, Development.

[14]  F. Sasaki,et al.  Internalization of styryl dye FM1-43 in the hair cells of lateral line organs in Xenopus larvae. , 1996, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[15]  R. K. Herman Touch sensation in Caenorhabditis elegans , 1996, BioEssays : news and reviews in molecular, cellular and developmental biology.

[16]  H. Wit,et al.  Low-voltage field-emission scanning electron microscopy of non-coated guinea-pig hair cell stereocilia , 1995, Hearing Research.

[17]  C. Kimmel,et al.  Stages of embryonic development of the zebrafish , 1995, Developmental dynamics : an official publication of the American Association of Anatomists.

[18]  C. Zuker,et al.  Genetic dissection of mechanosensory transduction: Mechanoreception-defective mutations of drosophila , 1994, Neuron.

[19]  S. Armstrong,et al.  REP-2, a Rab escort protein encoded by the choroideremia-like gene. , 1994, The Journal of biological chemistry.

[20]  C. Kimmel,et al.  The zebrafish midblastula transition. , 1993, Development.

[21]  Miguel C. Seabra,et al.  cDNA cloning of component A of Rab geranylgeranyl transferase and demonstration of its role as a Rab escort protein , 1993, Cell.

[22]  M. Boguski,et al.  MRS6 — yeast homologue of the choroideraemia gene , 1993, Nature Genetics.

[23]  T. Südhof,et al.  Purification of component A of Rab geranylgeranyl transferase: Possible identity with the choroideremia gene product , 1992, Cell.

[24]  T. Südhof,et al.  Rab geranylgeranyl transferase. A multisubunit enzyme that prenylates GTP-binding proteins terminating in Cys-X-Cys or Cys-Cys. , 1992, The Journal of biological chemistry.

[25]  R. Michelmore,et al.  Identification of markers linked to disease-resistance genes by bulked segregant analysis: a rapid method to detect markers in specific genomic regions by using segregating populations. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[26]  F. Cremers,et al.  Cloning of a gene that is rearranged in patients with choroideraemia , 1990, Nature.

[27]  A. J. Hudspeth,et al.  How the ear's works work , 1989, Nature.

[28]  B. Trask,et al.  Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21. , 1989, American journal of human genetics.

[29]  S Ayazi,et al.  Choroideremia, obesity, and congenital deafness. , 1981, American journal of ophthalmology.

[30]  C. Kimmel,et al.  The development and behavioral characteristics of the startle response in the zebra fish. , 1974, Developmental psychobiology.