A multiplex microsphere bead assay for comparative RNA expression analysis using flow cytometry

被引:23
作者
Fuja, T [1 ]
Hou, S
Bryant, P
机构
[1] Univ Calif Irvine, Ctr Dev Biol, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Flow Cytometry Facil, Irvine, CA 92697 USA
关键词
RNA expression; microsphere beads; quantitative real-time PCR; flow cytometry;
D O I
10.1016/j.jbiotec.2003.11.012
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
Comparative gene-expression profiling is an important tool in understanding molecular signatures of complex diseases as well as the responses of cells and tissues to external factors. With increasing microarray data, disease-specific molecular patterns are emerging but the acquisition of these data is expensive, difficult to customize and not well standardized. Once genome-wide scans identify differentially expressed genes in a given disease, cheaper, more easily customized methods will be needed for evaluating the expression of these genes in large population samples. Here we describe a novel multiplex microsphere bead assay (MBA) to compare gene expression levels. To test this assay we evaluated the expression levels of four transcripts (BRCA1, MGB1, DLG1 and ACT1) in normal and cancerous mammary tissue. The results were consistent with those generated by quantitative real-time PCR. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:193 / 205
页数:13
相关论文
共 36 条
  • [1] Fine scale mapping places DLG1, the gene encoding hDlg, telomeric to the OPA1 candidate region
    Alexander, C
    Stathakis, DG
    Lin, LH
    Rahman, S
    Bryant, PJ
    Auburger, G
    Chishti, AH
    [J]. MAMMALIAN GENOME, 1997, 8 (10) : 795 - 796
  • [2] Identification of mammaglobin B, a novel member of the uteroglobin gene family
    Becker, RM
    Darrow, C
    Zimonjic, DB
    Popescu, NC
    Watson, MA
    Fleming, TP
    [J]. GENOMICS, 1998, 54 (01) : 70 - 78
  • [3] Breast cancer revisited using DNA array-based gene expression profiling
    Bertucci, F
    Viens, P
    Hingamp, P
    Nasser, V
    Houlgatte, R
    Birnbaum, D
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2003, 103 (05) : 565 - 571
  • [4] Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays
    Bustin, SA
    [J]. JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2000, 25 (02) : 169 - 193
  • [5] Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems
    Bustin, SA
    [J]. JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2002, 29 (01) : 23 - 39
  • [6] Flow cytometry-based minisequencing: A new platform for high-throughput single-nucleotide polymorphism scoring
    Cai, H
    White, PS
    Torney, D
    Deshpande, A
    Wang, ZL
    Marrone, B
    Nolan, JP
    [J]. GENOMICS, 2000, 66 (02) : 135 - 143
  • [7] DeRisi J, 1996, NAT GENET, V14, P457
  • [8] Dimitrov SD, 2001, FOLIA BIOL-PRAGUE, V47, P120
  • [9] Quantitative analysis of BRCA1 and BRCA2 mRNA expression in sporadic breast carcinomas and its relationship with clinicopathological characteristics
    Egawa, C
    Miyoshi, Y
    Taguchi, T
    Tamaki, Y
    Noguchi, S
    [J]. JAPANESE JOURNAL OF CANCER RESEARCH, 2001, 92 (06): : 624 - 630
  • [10] Laser capture microdissection of paraffin-embedded tissues
    Ellsworth, DL
    Shriver, CD
    Ellsworth, RE
    Deyarmin, B
    Somiari, RI
    [J]. BIOTECHNIQUES, 2003, 34 (01) : 42 - +