Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2005-6-7
pubmed:abstractText
Fish otoliths are highly calcified concretions deposited in the inner ear and serve as a part of the hearing and balance systems. They consist mainly of calcium carbonate and a small amount of organic matrix. The latter component is considered to play important roles in otolith formation. Previously, we identified two major otolith matrix proteins, OMP-1 (otolith matrix protein-1) and Otolin-1, from salmonid species. To assess the function of these proteins in otolith formation, we performed antisense morpholino oligonucleotide (MO)-mediated knockdown of omp-1 and otolin-1 in zebrafish embryos. We first identified zebrafish cDNA homologs of omp-1 (zomp-1) and otolin-1 (zotolin-1). Whole-mount in situ hybridization then revealed that the expression of both zomp-1 and zotolin-1 mRNAs is restricted to the otic vesicles. zomp-1 mRNA was expressed from the 14-somite stage in the otic placode, but the zOMP-1 protein was detected only from 26-somite stage onwards. In contrast, zotolin-1 mRNA expression became clear around 72 hpf. MOs designed to inhibit zomp-1 and zotolin-1 mRNA translation, respectively, were injected into 1-2 cell stage embryos. zomp-1 MO caused a reduction in otolith size and an absence of zOtolin-1 deposition, while zotolin-1 MO caused a fusion of the two otoliths, and an increased instability of otoliths after fixation. We conclude that zOMP-1 is required for normal otolith growth and deposition of zOtolin-1 in the otolith, while zOtolin-1, a collagenous protein, is involved in the correct arrangement of the otoliths onto the sensory epithelium of the inner ear and probably in stabilization of the otolith matrix.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0925-4773
pubmed:author
pubmed:issnType
Print
pubmed:volume
122
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
791-803
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15905077-Amino Acid Sequence, pubmed-meshheading:15905077-Animals, pubmed-meshheading:15905077-Calcium Carbonate, pubmed-meshheading:15905077-Cloning, Molecular, pubmed-meshheading:15905077-DNA, Complementary, pubmed-meshheading:15905077-Ear, Inner, pubmed-meshheading:15905077-Extracellular Matrix Proteins, pubmed-meshheading:15905077-Gene Expression Regulation, Developmental, pubmed-meshheading:15905077-In Situ Hybridization, pubmed-meshheading:15905077-Microscopy, Video, pubmed-meshheading:15905077-Molecular Sequence Data, pubmed-meshheading:15905077-Nerve Tissue Proteins, pubmed-meshheading:15905077-Olfactory Marker Protein, pubmed-meshheading:15905077-Oligonucleotides, Antisense, pubmed-meshheading:15905077-Otolithic Membrane, pubmed-meshheading:15905077-Phalloidine, pubmed-meshheading:15905077-Phenotype, pubmed-meshheading:15905077-Protein Structure, Tertiary, pubmed-meshheading:15905077-RNA, Messenger, pubmed-meshheading:15905077-Time Factors, pubmed-meshheading:15905077-Zebrafish, pubmed-meshheading:15905077-Zebrafish Proteins
pubmed:year
2005
pubmed:articleTitle
Otolith matrix proteins OMP-1 and Otolin-1 are necessary for normal otolith growth and their correct anchoring onto the sensory maculae.
pubmed:affiliation
Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo, 113-8657 Tokyo, Japan. emur@pasteur.fr
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't