High RNA quality extracted from the tolerant crop Cyamopsis tetragonoloba (L.) despite possession of low RNA integrity number
Autor: | Saleh Alansi, Mohamed Tarroum, Abdel-Rhman Z. Gaafar, Norah Arrak Alenezi, Mohammad Nadeem, Aref Alshameri, Abdalrhaman M. Salih, Salim Khan, Fahad Al-Qurainy, Hassan O. Shaikhaldein |
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Rok vydání: | 2021 |
Předmět: |
0106 biological sciences
cyamopsis tetragonoloba 0303 health sciences Cyamopsis Guar RNA RNA integrity number Limiting Biology biology.organism_classification salinity tolerance 01 natural sciences Salinity Crop 03 medical and health sciences Agronomy rnaseq RNA extraction rna quality functional genomics TP248.13-248.65 rna extraction 030304 developmental biology 010606 plant biology & botany Biotechnology |
Zdroj: | Biotechnology & Biotechnological Equipment, Vol 35, Iss 1, Pp 608-618 (2021) |
ISSN: | 1314-3530 1310-2818 |
Popis: | Salinity is one of the most limiting constraints of crop production. Nevertheless, highly-tolerant crop plants (e.g. ‘Guar’ Cyamopsis tetragonoloba) can thrive well under salinity conditions. RNA-Seq plays a central role in identifying genes involved in the response mechanisms to salt stress in plant species. High-quality RNA, free of genomic DNA is a critical determinant for success in subsequent downstream experiments to shed light on tolerance mechanisms. In this research, an inspection of two different total RNA isolation protocols was employed for preparing highly pure and intact RNAs with good yield from Guar tissue under both high salinity and control conditions. The extracted RNA appeared in all quality metrics to be of adequate quantity and quality for most downstream applications, including high-throughput transcriptome sequencing and expression analysis. However, the outcomes showed that the most widely used RNA quality measurement, the RNA Integrity Number (RIN), is a poor indicator with a weak correlation to the integrity of RNA from this plant. In contrast to human and animal cells, plants have various ribosomal RNA species. Consequently, whenever the RNA was separated on an agarose gel, several RNA bands did appear, which gives the false impression of being unable to analyze the results of the bioanalyzer integrity. Low RIN number RNA samples were further processed by RNA-sequencing RNA-seq experiments from guar. RNA-seq analysis via Illumina’s paired-end method was carried out to trace back and evaluate the extracted total RNA, resulting in high-quality data for subsequent stress tolerance research. |
Databáze: | OpenAIRE |
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