AI Article Synopsis

  • - Recent research indicates that 70% ethanol is more effective than formalin for preserving mRNA in brain tissues, yielding better RNA quality and quantity for gene expression studies.
  • - Ethanol-fixed tissues maintained 70% of RNA yield compared to fresh frozen samples, while formalin-fixed tissues provided almost no recoverable RNA, affecting the success of RT-PCR tests.
  • - Overall, immersion in 70% ethanol not only preserves RNA integrity but also ensures comparable histology and better immunostaining results compared to formalin, making it a superior choice for future tissue studies.

Article Abstract

Although RNA can be retrieved from formalin-fixed, paraffin-embedded (FFPE) tissues, the yield is low, and the RNA is fragmented. Recent advances in gene expression profiling underscore the importance of identifying a fixative that preserves histology and mRNA. We demonstrated that, for immersion fixation of brains, 70% ethanol is superior to formalin for mRNA preservation. RNA yield from ethanol-fixed tissues was 70% of the yield from fresh frozen specimens, but only a negligible quantity was recovered from formalin-fixed tissues. RNA from ethanol-fixed brains showed integrity comparable to RNA from fresh frozen tissues, and RT-PCR using RNA from ethanol-fixed tissues was consistently successful. RNA from FFPE tissues composed of low-molecular weight fragments, and their use in RT-PCR failed repeatedly. The yield and quality of RNA from ethanol-fixed brains were unaffected after immersion at 4 degrees C for 2 weeks. In a blinded comparison to FFPE tissues, ethanol-fixed specimens were judged to show comparable histology and superior immunostaining. After laser capture microdissection (LCM), we failed to recover mRNA from FFPE tissues but retrieved mRNA from ethanol-fixed tissues for RT-PCR and cDNA microarray analysis. We conclude that 70% ethanol preserves RNA integrity and is suitable for expression profiling of brain tissues by LCM and cDNA microarray.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096012PMC
http://dx.doi.org/10.1111/j.1750-3639.2004.tb00050.xDOI Listing

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