Visualizing the needle in the haystack: In situ hybridization with fluorescent dendrimers

Jacquelyn Gerhart, M. Baytion, J. Perlman, C. Neely, B. Hearon, T. Nilsen, R. Getts, J. Kadushin, Mindy George-Weinstein

Research output: Contribution to journalArticlepeer-review

Abstract

In situ hybridization with 3DNA dendrimers is a novel tool for detecting low levels of mRNA in tissue sections and whole embryos. Fluorescently labeled dendrimers were used to identify cells that express mRNA for the skeletal muscle transcription factor MyoD in the early chick embryo. A small population of MyoD mRNA positive cells was found in the epiblast prior to the initiation of gastrulation, two days earlier than previously detected using enzymatic or radiolabeled probes for mRNA. When isolated from the epiblast and placed in culture, the MyoD mRNA positive cells were able to differentiate into skeletal muscle cells. These results demonstrate that DNA dendrimers are sensitive and precise tools for identifying low levels of mRNA in single cells and tissues.

Original languageAmerican English
JournalBiological Procedures Online
Volume6
StatePublished - Jan 1 2004

Keywords

  • DNA
  • In situ hybridization
  • MyoD protein
  • animal cell
  • animal tissue
  • article
  • cell culture
  • cell differentiation
  • cell isolation
  • cell population
  • chick embryo
  • controlled study
  • dendrimer
  • ectoderm
  • embryo
  • embryonal tissue
  • fluorescent dye
  • g
  • gastrulation
  • messenger RNA

Disciplines

  • Developmental Biology

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