Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/14880
Title: EFFICIENT RNA EXTRACTION PROTOCOL FOR THE WOOD MANGROVE SPECIES LAGUNCULARIA RACEMOSA SUITED FOR NEXT-GENERATION RNA SEQUENCING
Authors: WILWERTH, MAURICIO WOLF
ROSSETTO, PRISCILLA DE BARROS
REINERT, FERNANDA
PEIXOTO, RAQUEL SOARES
FERREIRA, MÁRCIO ALVES-
Keywords: L. racemosa
RNA isolation
RT-PCR
Mangrove
Guanidine (iso) thiocyanate
Issue Date: 2-May-2016
Publisher: Karachi: Pakistan Journal of Botany , Botanical garden , University of Karachi
Citation: Wilwerth, M. W., Rossetto, P. D. B., Reinert, F., Peixoto, R. S., & Ferreir, M. A. (2016). Efficient RNA extraction protocol for the wood mangrove species Laguncularia racemosa suited for next-generation RNA sequencing. Pakistan Journal of Botany, 48(2), 661-672.
Abstract: Mangrove flora and habitat have immeasurable importance in marine and coastal ecology as well as in the economy. Despite their importance, they are constantly threatened by oil spill accidents and environmental contamination; therefore, it is crucial to understand the changes in gene expression to better predict toxicity in these plants. Among the species of Atlantic coast mangrove (Americas and Africa), Laguncularia racemosa, or white mangrove, is a conspicuous species. The wide distribution of L. racemosa in areas where marine oil exploration is rapidly increasing make it a candidate mangrove species model to uncover the impact of oil spills at the molecular level with the use of massive transcriptome sequencing. However, for this purpose, the RNA extraction protocol should ensure low levels of contaminants and structure integrity. In this study, eight RNA extraction methods were tested and analysed using downstream applications. The InviTrap Spin Plant RNA Mini Kit performed best with regard to purity and integrity. Moreover, the obtained RNA was submitted to cDNA synthesis and RT-PCR, successfully generating amplification products of the expected size. These results show the applicability of the RNA obtained here for downstream methodologies, such as the construction of cDNA libraries for the Illumina Hi-seq platform.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/14880
Appears in Collections:2006,Part-1

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