Identification of unique transcripts from a mouse full-length, subtracted inner ear cDNA library

被引:15
|
作者
Beisel, KW
Shiraki, T
Morris, KA
Pompeia, C
Kachar, B
Arakawa, T
Bono, H
Kawai, J
Hayashizaki, Y
Carninci, P
机构
[1] Creighton Univ, Dept Biomed Sci, Omaha, NE 68178 USA
[2] RIKEN, Genom Sci Ctr, Lab Genome Explorat, Res Grp, Tsukuba, Ibaraki, Japan
[3] NIDCD, Sect Struct Cell Biol, Natl Inst Hlth, Bethesda, MD 20892 USA
关键词
D O I
10.1016/j.ygeno.2004.01.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A small-scale full-length library construction approach was developed to facilitate production of a mouse full-length cDNA encyclopedia representing similar to 250 enriched, normalized, and/or Subtracted cDNA libraries. One library produced using this approach was a subtracted adult mouse inner car cDNA library (sIEa). The average size of the inserts was similar to 2.5 kb, with the majority ranging from 0.5 to 7.0 kb. From this library 22,574 sequence reads were obtained from 15,958 independent clones. Sequencing and chromosomal localization established 5240 clusters, with 1302 clusters being unique and 359 representing new ESTs. Our sIEa library contributed 56.1% of the 7773 nonredundant Unigene clusters associated with the four mouse inner ear libraries in the NCBI dbEST. Based on homologous chromosomal regions between human and mouse, we identified 1018 UniGene clusters associated with the deafness locus critical regions. Of these, 59 clusters were found only in our sIEa library and represented similar to 50% of the identified critical regions. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1012 / 1023
页数:12
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