Key result
Proteinase K treatment and RNA STAT-60 extraction successfully isolate mRNA for RT-PCR from formalin-fixed tissue.
Why the study?
Fresh tissue from sudden infant death syndrome cases is scarce, necessitating methods to isolate mRNA from formalin fixed, paraffin wax embedded archival tissue for RT-PCR analysis.
This method enables the extraction of mRNA suitable for RT-PCR from archival formalin-fixed, paraffin-embedded tissues, facilitating retrospective gene expression studies.
Answers are grounded in this paper and cite their sources.
Allows retrospective cytokine analysis from archival animal tissues; leaves open human validation.
Fresh tissue from cases of sudden infant death syndrome is becoming increasingly scarce and therefore researchers interesting in studying the aetiology of this syndrome have had to resort to archival tissue, usually in the form of paraffin wax sections. A simple method for isolating mRNA from formalin fixed, paraffin wax embedded material of sufficient purity for reverse transcription (RT)-PCR is described. Proteinase K treatment of formalin fixed, wax embedded tissue followed by RNA STAT-60 extraction was successful in isolating mRNA suitable for RT-PCR. Interleukin (IL)-1alpha, IL-6 and tumour necrosis factor (TNF) transcripts were amplified successfully from heart, but not thyroid, kidney or liver tissue, of a patient who died following rejection of a transplanted heart, and IL-1alpha, but not IL-6 or TNF, transcripts from lung tissue of a six month old baby who died of viral pneumonia. Transcripts of a housekeeping gene were detected in all tissues. This method should be useful for examining gene expression in archival material.
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Bevan et al. (1996) studied Formalin-fixed tissue analysis (n=2). Proteinase K treatment followed by RNA STAT-60 extraction was evaluated on Successful amplification of cytokine mRNA (IL-1alpha, IL-6, TNF) and housekeeping gene transcripts. Proteinase K treatment of formalin-fixed, wax-embedded tissue followed by RNA STAT-60 extraction successfully isolated mRNA suitable for RT-PCR amplification of cytokine transcripts.
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