4.6 Article

Simplified protocol modification of TRIzol method for extraction of high-quality RNA yield from RNase-rich rat pancreas

Journal

PROCESS BIOCHEMISTRY
Volume 130, Issue -, Pages 464-471

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.procbio.2023.04.029

Keywords

RNA extraction; RNase-rich pancreas; TRIzol; Quantitative-PCR

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This study modified the standard TRIzol RNA extraction method to establish a reproducible, applicable, and efficient protocol for extracting intact RNA from RNase-rich rat pancreas. The modified protocol yielded significantly higher RNA concentration and improved RNA purity compared to the standard protocol. RT-qPCR analysis also showed that the RNA extracted using the modified protocol had better quality, reflected by decreased Ct values.
The extraction of a sufficient quantity of intact RNA from RNase-rich rat pancreas for estimation of gene transcript levels has been a long-standing challenge. This study provided simple modifications in the steps involved in the standard TRIzol RNA extraction method to set up a reproducible, applicable, and efficient protocol to be routinely used in the laboratory. A Nanodrop spectrophotometer was used to evaluate the RNA concentration, and purity (A260/A280, and A260/A230 absorbent ratios). Gel electrophoresis was used to assess RNA integrity. Further analysis included sequential RT-qPCR of a housekeeping gene to evaluate the optimized protocol. The current study demonstrated that the modified protocol rendered significantly more RNA concentration (mean: 635.8 +/- 210.5 ng/mu L) compared to the standard protocol (mean: 77.2 +/- 25.9 ng/mu L). Moreover, the modified protocol produced an improvement in the RNA purity (mean :A260/A280 ratio = 1.89 +/- 0.13; A260/A230 ratio = 1.7 +/- 0.16) compared to the standard protocol (mean: A260/A280 ratio = 1.7 +/- 0.26; A260/A230 ratio = 2.5 +/- 1.9). Additionally, RT-qPCR analysis revealed that the RNA extracted using the modified protocol resulted in significantly decreased (P < 0.001) Ct values (decreased by 6 Ct units) compared to the standard protocol, reflecting the good quality of the RNA. Conclusion: This study succeeded in providing golden tips to extract a high yield of good-quality RNA from RNase-rich rat pancreas for the sequential gene expression assays.

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