共 49 条
Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear
被引:28
作者:

Peters, Linda M.
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Sect Human Genet, Mol Genet Lab, NIGMS, Rockville, MD 20850 USA

Belyantseva, Inna A.
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Sect Human Genet, Mol Genet Lab, NIGMS, Rockville, MD 20850 USA

Lagziel, Ayala
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Sect Human Genet, Mol Genet Lab, NIGMS, Rockville, MD 20850 USA

Battey, James F.
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Sect Human Genet, Mol Genet Lab, NIGMS, Rockville, MD 20850 USA

Friedman, Thomas B.
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Sect Human Genet, Mol Genet Lab, NIGMS, Rockville, MD 20850 USA

Morell, Robert J.
论文数: 0 引用数: 0
h-index: 0
机构:
Natl Inst Deafness & Other Commun Disorders, Sect Human Genet, Mol Genet Lab, NIGMS, Rockville, MD 20850 USA Natl Inst Deafness & Other Commun Disorders, Sect Human Genet, Mol Genet Lab, NIGMS, Rockville, MD 20850 USA
机构:
[1] Natl Inst Deafness & Other Commun Disorders, Sect Human Genet, Mol Genet Lab, NIGMS, Rockville, MD 20850 USA
[2] Natl Inst Neurol Disorders & Stroke, G Prot Coupled Receptors Sect, NIH, Bethesda, MD 20892 USA
来源:
关键词:
ear;
inner;
MPSS;
transcription;
genetic;
Vmo1;
Slc26a5;
D O I:
10.1016/j.ygeno.2006.09.006
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:
Specialization in cell function and morphology is influenced by the differential expression of mRNAs, many of which are expressed at low abundance and restricted to certain cell types. Detecting such transcripts in cDNA libraries may require sequencing millions of clones. Massively parallel signature sequencing (MPSS) is well suited to identifying transcripts that are expressed in discrete cell types and in low abundance. We have made MPSS libraries from microdissections of three inner ear tissues. By comparing these MPSS libraries to those of 87 other tissues included in the Mouse Reference Transcriptome online resource, we have identified genes that are highly enriched in, or specific to, the inner ear. We show by RT-PCR and in situ hybridization that signatures unique to the inner ear libraries identify transcripts with highly specific cell-type localizations. These transcripts serve to illustrate the utility of a resource that is available to the research community. Utilization of these resources will increase the number of known transcription units and expand our knowledge of the tissue-specific regulation of the transcriptome. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:197 / 206
页数:10
相关论文
共 49 条
[31]
INFORMATION CODING IN THE OLFACTORY SYSTEM - EVIDENCE FOR A STEREOTYPED AND HIGHLY ORGANIZED EPITOPE MAP IN THE OLFACTORY-BULB
[J].
RESSLER, KJ
;
SULLIVAN, SL
;
BUCK, LB
.
CELL,
1994, 79 (07)
:1245-1255

RESSLER, KJ
论文数: 0 引用数: 0
h-index: 0
机构: Department of Neurobiology Harvard Medical School Boston

SULLIVAN, SL
论文数: 0 引用数: 0
h-index: 0
机构: Department of Neurobiology Harvard Medical School Boston

BUCK, LB
论文数: 0 引用数: 0
h-index: 0
机构: Department of Neurobiology Harvard Medical School Boston
[32]
A catalog of stability-associated sequence elements in 3′ UTRs of yeast mRNAs -: art. no. R86
[J].
Shalgi, R
;
Lapidot, M
;
Shamir, R
;
Pilpel, Y
.
GENOME BIOLOGY,
2005, 6 (10)

论文数: 引用数:
h-index:
机构:

Lapidot, M
论文数: 0 引用数: 0
h-index: 0
机构: Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel

Shamir, R
论文数: 0 引用数: 0
h-index: 0
机构: Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel

Pilpel, Y
论文数: 0 引用数: 0
h-index: 0
机构:
Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[33]
Initial characterization of an uromodulin-like 1 gene on human chromosome 21q22.3
[J].
Shibuya, K
;
Nagamine, K
;
Okui, M
;
Ohsawa, Y
;
Asakawa, S
;
Minoshima, S
;
Hase, T
;
Kudoh, J
;
Shimizu, N
.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,
2004, 319 (04)
:1181-1189

Shibuya, K
论文数: 0 引用数: 0
h-index: 0
机构: Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan

Nagamine, K
论文数: 0 引用数: 0
h-index: 0
机构: Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan

Okui, M
论文数: 0 引用数: 0
h-index: 0
机构: Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan

Ohsawa, Y
论文数: 0 引用数: 0
h-index: 0
机构: Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan

Asakawa, S
论文数: 0 引用数: 0
h-index: 0
机构: Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan

Minoshima, S
论文数: 0 引用数: 0
h-index: 0
机构: Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan

Hase, T
论文数: 0 引用数: 0
h-index: 0
机构: Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan

Kudoh, J
论文数: 0 引用数: 0
h-index: 0
机构: Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan

Shimizu, N
论文数: 0 引用数: 0
h-index: 0
机构: Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan
[34]
Targeted disruption of Otog results in deafness and severe imbalance
[J].
Simmler, MC
;
Cohen-Salmon, M
;
El-Amraoui, A
;
Guillaud, L
;
Benichou, JC
;
Petit, C
;
Panthier, JJ
.
NATURE GENETICS,
2000, 24 (02)
:139-143

Simmler, MC
论文数: 0 引用数: 0
h-index: 0
机构:
Ecole Natl Vet, INRA Genet Mol & Cellulaire, UMR 955, Maisons Alfort, France Ecole Natl Vet, INRA Genet Mol & Cellulaire, UMR 955, Maisons Alfort, France

Cohen-Salmon, M
论文数: 0 引用数: 0
h-index: 0
机构: Ecole Natl Vet, INRA Genet Mol & Cellulaire, UMR 955, Maisons Alfort, France

El-Amraoui, A
论文数: 0 引用数: 0
h-index: 0
机构: Ecole Natl Vet, INRA Genet Mol & Cellulaire, UMR 955, Maisons Alfort, France

Guillaud, L
论文数: 0 引用数: 0
h-index: 0
机构: Ecole Natl Vet, INRA Genet Mol & Cellulaire, UMR 955, Maisons Alfort, France

Benichou, JC
论文数: 0 引用数: 0
h-index: 0
机构: Ecole Natl Vet, INRA Genet Mol & Cellulaire, UMR 955, Maisons Alfort, France

Petit, C
论文数: 0 引用数: 0
h-index: 0
机构: Ecole Natl Vet, INRA Genet Mol & Cellulaire, UMR 955, Maisons Alfort, France

Panthier, JJ
论文数: 0 引用数: 0
h-index: 0
机构: Ecole Natl Vet, INRA Genet Mol & Cellulaire, UMR 955, Maisons Alfort, France
[35]
Animal microRNAs confer robustness to gene expression and have a significant impact on 3′UTR evolution
[J].
Stark, A
;
Brennecke, J
;
Bushati, N
;
Russell, RB
;
Cohen, SM
.
CELL,
2005, 123 (06)
:1133-1146

Stark, A
论文数: 0 引用数: 0
h-index: 0
机构:
European Mol Biol Lab, D-69117 Heidelberg, Germany European Mol Biol Lab, D-69117 Heidelberg, Germany

Brennecke, J
论文数: 0 引用数: 0
h-index: 0
机构:
European Mol Biol Lab, D-69117 Heidelberg, Germany European Mol Biol Lab, D-69117 Heidelberg, Germany

Bushati, N
论文数: 0 引用数: 0
h-index: 0
机构:
European Mol Biol Lab, D-69117 Heidelberg, Germany European Mol Biol Lab, D-69117 Heidelberg, Germany

Russell, RB
论文数: 0 引用数: 0
h-index: 0
机构:
European Mol Biol Lab, D-69117 Heidelberg, Germany European Mol Biol Lab, D-69117 Heidelberg, Germany

Cohen, SM
论文数: 0 引用数: 0
h-index: 0
机构:
European Mol Biol Lab, D-69117 Heidelberg, Germany European Mol Biol Lab, D-69117 Heidelberg, Germany
[36]
Type IX collagen knock-out mouse shows progressive hearing loss
[J].
Suzuki, N
;
Asamura, K
;
Kikuchi, Y
;
Takumi, Y
;
Abe, S
;
Imamura, Y
;
Hayashi, T
;
Aszodi, A
;
Fässler, R
;
Usami, S
.
NEUROSCIENCE RESEARCH,
2005, 51 (03)
:293-298

Suzuki, N
论文数: 0 引用数: 0
h-index: 0
机构: Shinshu Univ, Sch Med, Dept Otorhinolaryngol, Matsumoto, Nagano 3908621, Japan

Asamura, K
论文数: 0 引用数: 0
h-index: 0
机构: Shinshu Univ, Sch Med, Dept Otorhinolaryngol, Matsumoto, Nagano 3908621, Japan

Kikuchi, Y
论文数: 0 引用数: 0
h-index: 0
机构: Shinshu Univ, Sch Med, Dept Otorhinolaryngol, Matsumoto, Nagano 3908621, Japan

Takumi, Y
论文数: 0 引用数: 0
h-index: 0
机构: Shinshu Univ, Sch Med, Dept Otorhinolaryngol, Matsumoto, Nagano 3908621, Japan

Abe, S
论文数: 0 引用数: 0
h-index: 0
机构: Shinshu Univ, Sch Med, Dept Otorhinolaryngol, Matsumoto, Nagano 3908621, Japan

Imamura, Y
论文数: 0 引用数: 0
h-index: 0
机构: Shinshu Univ, Sch Med, Dept Otorhinolaryngol, Matsumoto, Nagano 3908621, Japan

Hayashi, T
论文数: 0 引用数: 0
h-index: 0
机构: Shinshu Univ, Sch Med, Dept Otorhinolaryngol, Matsumoto, Nagano 3908621, Japan

Aszodi, A
论文数: 0 引用数: 0
h-index: 0
机构: Shinshu Univ, Sch Med, Dept Otorhinolaryngol, Matsumoto, Nagano 3908621, Japan

Fässler, R
论文数: 0 引用数: 0
h-index: 0
机构: Shinshu Univ, Sch Med, Dept Otorhinolaryngol, Matsumoto, Nagano 3908621, Japan

Usami, S
论文数: 0 引用数: 0
h-index: 0
机构: Shinshu Univ, Sch Med, Dept Otorhinolaryngol, Matsumoto, Nagano 3908621, Japan
[37]
A new allelic series for the underwhite gene on mouse chromosome 15
[J].
Sweet, HO
;
Brilliant, MH
;
Cook, SA
;
Johnson, KR
;
Davisson, MT
.
JOURNAL OF HEREDITY,
1998, 89 (06)
:546-551

Sweet, HO
论文数: 0 引用数: 0
h-index: 0
机构: Jackson Lab, Bar Harbor, ME 04609 USA

Brilliant, MH
论文数: 0 引用数: 0
h-index: 0
机构: Jackson Lab, Bar Harbor, ME 04609 USA

Cook, SA
论文数: 0 引用数: 0
h-index: 0
机构: Jackson Lab, Bar Harbor, ME 04609 USA

Johnson, KR
论文数: 0 引用数: 0
h-index: 0
机构: Jackson Lab, Bar Harbor, ME 04609 USA

Davisson, MT
论文数: 0 引用数: 0
h-index: 0
机构: Jackson Lab, Bar Harbor, ME 04609 USA
[38]
Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease
[J].
Tufarelli, C
;
Stanley, JAS
;
Garrick, D
;
Sharpe, JA
;
Ayyub, H
;
Wood, WG
;
Higgs, DR
.
NATURE GENETICS,
2003, 34 (02)
:157-165

Tufarelli, C
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England

Stanley, JAS
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England

Garrick, D
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England

Sharpe, JA
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England

Ayyub, H
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England

Wood, WG
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England

Higgs, DR
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England Univ Oxford, MRC, Mol Haematol Unit, Weatherall Inst Mol Med,John Radcliffe Hosp, Oxford OX3 9DS, England
[39]
SERIAL ANALYSIS OF GENE-EXPRESSION
[J].
VELCULESCU, VE
;
ZHANG, L
;
VOGELSTEIN, B
;
KINZLER, KW
.
SCIENCE,
1995, 270 (5235)
:484-487

VELCULESCU, VE
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV, CTR ONCOL, HOWARD HUGHES MED INST, BALTIMORE, MD 21231 USA

ZHANG, L
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV, CTR ONCOL, HOWARD HUGHES MED INST, BALTIMORE, MD 21231 USA

VOGELSTEIN, B
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV, CTR ONCOL, HOWARD HUGHES MED INST, BALTIMORE, MD 21231 USA

KINZLER, KW
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV, CTR ONCOL, HOWARD HUGHES MED INST, BALTIMORE, MD 21231 USA
[40]
Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment
[J].
Verhoeven, K
;
Van Laer, L
;
Kirschhofer, K
;
Legan, PK
;
Hughes, DC
;
Schatteman, I
;
Verstreken, M
;
Van Hauwe, P
;
Coucke, P
;
Chen, A
;
Smith, RJH
;
Somers, T
;
Offeciers, FE
;
Van de Heyning, P
;
Richardson, GP
;
Wachtler, F
;
Kimberling, WT
;
Willems, PJ
;
Govaerts, PJ
;
Van Camp, G
.
NATURE GENETICS,
1998, 19 (01)
:60-62

Verhoeven, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Van Laer, L
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Kirschhofer, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Legan, PK
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Hughes, DC
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Schatteman, I
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Verstreken, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Van Hauwe, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Coucke, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Chen, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Smith, RJH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Somers, T
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Offeciers, FE
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Van de Heyning, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Richardson, GP
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Wachtler, F
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Kimberling, WT
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Willems, PJ
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Govaerts, PJ
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium

Van Camp, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Instelling Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium