Abstract

One serviceable feature of in situ hybridization is its potential for assessing relative levels of mRNA in specific regions of tissues and organs. To determine its efficacy as a quantitative technique, we applied a nested factorial design to a multifactorial experiment. Estimates of the magnitude of variance components then allowed an assessment of variation over samples of sections from the same tissue source, variation in label over 2 anatomical sites within the same section of tissue, as well as experiment-to-experiment variation. We found approximately 51% of the total variance arose from experiment-to-experiment variation, while approximately 21% of the total variance was due to variation in autoradiography grain density over neurons in the same brain region. Rat-to-rat variation accounted for approximately 11%. About 10% of the variance was due to variation between sections of tissue that were derived from the same tissue source and were hybridized in the same hybridization experiment. Variation between 2 homologous, bilaterally located brain regions located on the same tissue section (the right and left supraoptic nucleus), accounted for approximately 5% of the total variance. The remaining unaccounted error variance was approximately 2% of the total variance. Since an expected change in cellular content of a particular mRNA was observed as a function of experimental treatment, results suggest in situ hybridization is a useful quantitative method.(ABSTRACT TRUNCATED AT 250 WORDS)

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