A comparison of commercially-available automated and manual extraction kits for the isolation of total RNA from small tissue samples

被引:49
|
作者
Jeffries, Marlo K. Sellin [1 ,2 ]
Kiss, Andor J. [2 ,3 ]
Smith, Austin W. [2 ]
Oris, James T. [2 ]
机构
[1] Texas Christian Univ, Dept Biol, Ft Worth, TX 76129 USA
[2] Miami Univ, Dept Biol, Oxford, OH 45056 USA
[3] Miami Univ, Ctr Bioinformat & Funct Genom, Oxford, OH 45056 USA
来源
BMC BIOTECHNOLOGY | 2014年 / 14卷
关键词
RNA extraction; Gene expression; qPCR; RNA-Seq; Next generation sequencing; Microarray; Small tissues; Fathead minnow; MESSENGER-RNA; BLOOD RNA; QUALITY; DNA; INTEGRITY; IMPACT; PCR;
D O I
10.1186/s12896-014-0094-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: This study compared the performance of five commercially available kits in extracting total RNA from small eukaryotic tissue samples (<15 mg). Total RNA was isolated from fathead minnow (Pimephales promelas) tissues (spleen, blood, kidney, embryo, and larvae) using the Qiagen RNeasy (R) Plus Mini, Qiagen RNeasy (R) Plus Universal, Promega Maxwell (R) 16 LEV simplyRNA, Ambion MagMAX (TM)-96 and Promega SimplyRNA HT kits. Kit performance was evaluated via measures of RNA quantity (e.g., total RNA amount) and quality (e.g., ratio of absorbance at 260 and 280 nm, RNA integrity number (RIN), presence of gDNA). Results: With the exception of embryos, each kit generally extracted >= 5 mu g of total RNA from each sample. With regard to RNA quality, the RINs of RNA samples isolated via the Plus Mini and Maxwell (R) 16 kits were consistently higher than those of samples extracted via the remaining three kits and for all tissues, these kits produced intact RNA with average RIN values >= 7. The Plus Universal and SimplyRNA HT kits produced moderately degraded (RIN values <7, but >= 5), while the RNA recovered via the MagMAX (TM) kit tended to exhibit a high degree of degradation (RIN values <5). Conclusions: Each kit was generally capable of extracting the amount of RNA required for most downstream gene expression applications suggesting that RNA yield is unlikely to be a limiting factor for any of the kits evaluated. However, differences in the quality of RNA extracted via each of the kits indicate that these kits may differ in their ability to yield RNA acceptable for some applications. Overall, the findings of this study demonstrate that there are practical differences between commercially available RNA extraction kits that should be taken into account when selecting extraction methods to be used for isolating RNA designated for gene expression analysis.
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