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Amine-modified random primers to label probes for DNA microarrays

  1. Author:
    Xiang, C. C.
    Kozhich, O. A.
    Chen, M.
    Inman, J. M.
    Phan, Q. N.
    Chen, Y. D.
    Brownstein, M. J.
  2. Author Address

    NIMH, Genet Lab, NIH, Bethesda, MD 20892 USA NIMH, Genet Lab, NIH, Bethesda, MD 20892 USA NHGRI, Canc Genet Branch, NIH, Bethesda, MD 20892 USA SAIC Frederick, Frederick, MD 21702 USA Brownstein MJ NIMH, Genet Lab, NIH, Bethesda, MD 20892 USA
    1. Year: 2002
  1. Journal: Nature Biotechnology
    1. 20
    2. 7
    3. Pages: 738-742
  2. Type of Article: Article
  1. Abstract:

    DNA microarrays have been used to study the expression of thousands of genes at the same time in a variety of cells and tissues(1-3). The methods most commonly used to label probes for microarray studies require a minimum of 20 mug of total RNA or 2 mug of poly(A) RNA(4,5). This has made it difficult to study small and rare tissue samples. RNA amplification techniques and improved labeling methods have recently been described(6-9). These new procedures and reagents allow the use of less input RNA, but they are relatively time-consuming and expensive. Here we introduce a technique for preparing fluorescent probes that can be used to label as little as 1 mug of total RNA. The method is based on priming cDNA synthesis with random hexamer oligonucleotides, on the 5' ends of which are bases with free amino groups. These amine-modified primers are incorporated into the cDNA along with aminoallyl nucleotides, and fluorescent dyes are then chemically added to the free amines. The method is simple to execute, and amine- reactive dyes are considerably less expensive than dye-labeled bases or dendrimers.

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