In silico analyses of mouse inner-ear transcripts

被引:14
作者
Klockars, T
Perheentupa, T
Dahl, HHM
机构
[1] Univ Melbourne, Murdoch Childrens Res Inst, Dept Gene Identificat, Royal Childrens Hosp, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Dept Paediat, Parkville, Vic 3052, Australia
[3] Natl Publ Hlth Inst, Dept Mol Med, Biomedicum, Helsinki, Finland
来源
JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY | 2003年 / 4卷 / 01期
关键词
mouse; inner ear; gene expression;
D O I
10.1007/s10162-002-2058-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The development and function of the inner ear is complex requiring the correct and coordinated expression of many genes. The recent progress in the analyses of the human and other genomes has provided tools for identification of genes involved in hearing. As more and more nucleotide sequence information accumulates, experimental methods of molecular biology are rapidly being supplemented, and partially supplanted, by computational methods. In this study we present comprehensive in silico analyses of a cDNA library representing almost 1600 transcripts isolated from mouse inner ear. By mining the public databases we were able to rapidly and efficiently identify numerous transcripts likely to have a specific role in the auditory or vestibular function of the inner ear. Analyses revealed about 600 known genes and almost 100 inner-ear specific transcripts. Almost 50 of these are candidate genes for hearing impairment based on their chromosomal localization and inner-ear expression pattern. We describe a powerful approach to identify novel genes associated with hearing and vestibular function, further increasing our understanding of the molecular biology of the inner ear.
引用
收藏
页码:24 / 40
页数:17
相关论文
共 67 条
[1]   Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F [J].
Ahmed, ZM ;
Riazuddin, S ;
Bernstein, SL ;
Ahmed, Z ;
Khan, S ;
Griffith, AJ ;
Morell, RJ ;
Friedman, TB ;
Riazuddin, S ;
Wilcox, ER .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (01) :25-34
[2]   Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F [J].
Alagramam, KN ;
Yuan, HJ ;
Kuehn, MH ;
Murcia, CL ;
Wayne, S ;
Srisailpathy, CRS ;
Lowry, RB ;
Knaus, R ;
Van Laer, L ;
Bernier, FP ;
Schwartz, S ;
Lee, C ;
Morton, CC ;
Mullins, RF ;
Ramesh, A ;
Van Camp, G ;
Hagemen, GS ;
Woychik, RP ;
Smith, RJH .
HUMAN MOLECULAR GENETICS, 2001, 10 (16) :1709-1718
[3]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[4]  
Ansari-Lari MA, 1998, GENOME RES, V8, P29
[5]   Large-scale sequencing in human chromosome 12p13: Experimental and computational gene structure determination [J].
AnsariLari, MA ;
Shen, Y ;
Muzny, DM ;
Lee, W ;
Gibbs, RA .
GENOME RESEARCH, 1997, 7 (03) :268-280
[6]  
Bartles JR, 1996, J CELL SCI, V109, P1229
[7]   Processing and analyzing the mouse temporal bone to identify gross, cellular and subcellular pathology [J].
Bohne, BA ;
Harding, GW .
HEARING RESEARCH, 1997, 109 (1-2) :34-45
[8]   Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23 [J].
Bork, JM ;
Peters, LM ;
Riazuddin, S ;
Bernstein, SL ;
Ahmed, ZM ;
Ness, SL ;
Polomeno, R ;
Ramesh, A ;
Schloss, M ;
Srisailpathy, CRS ;
Wayne, S ;
Bellman, S ;
Desmukh, D ;
Ahmed, Z ;
Khan, SN ;
Kaloustian, VMD ;
Li, XC ;
Lalwani, A ;
Riazuddin, S ;
Bitner-Glindzicz, M ;
Nance, WE ;
Liu, XZ ;
Wistow, G ;
Smith, RJH ;
Griffith, AJ ;
Wilcox, ER ;
Friedman, TB ;
Morell, RJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (01) :26-37
[9]   A novel putative transporter maps to the osteosclerosis (oc) mutation and is not expressed in the oc mutant mouse [J].
Brady, KP ;
Dushkin, H ;
Förnzler, D ;
Koike, T ;
Magner, F ;
Her, H ;
Gullans, S ;
Segre, GV ;
Green, RM ;
Beier, DR .
GENOMICS, 1999, 56 (03) :254-261
[10]   I-mf, a novel myogenic repressor, interacts with members of the MyoD family [J].
Chen, CMA ;
Kraut, N ;
Groudine, M ;
Weintraub, H .
CELL, 1996, 86 (05) :731-741