Dna Barcoding: Efficiency of Rbcl Gene for Sequence Characterisation of Cyperus Esculentus in Nigeria

Author:

Bello Ridwan Opeyemi1ORCID,Ojokoh Anthony Okhonlaye2,Babalola Deborah3,Shonde. Temitope Esther3,Towobola Funmilayo Mary3

Affiliation:

1. Federal University of Technology Akure

2. Federal University of Technology Akure School of Sciences

3. International Institute of Tropical Agriculture

Abstract

AbstractBackground Plants have been classified based on morphological traits. However, there are biases associated with this classification. The limitation can be prevented by using DNA barcoding. Therefore, the efficiency of the Ribulose -bisphosphate carboxylase (rbcL) marker was investigated to identify Tiger Nut (Cyperus esculentus), which belongs to the family of Cyperaceae. In this study,C. esculentussamples were collected from two villages in northern Nigeria. For DNA barcoding, the rbcL region ofC. esculentussamples were amplified, sequenced in both directions, and subsequently analysed. The amplified sequences' biological sequence homology, sequence divergence, and phylogenetic tree construction were studied using Basic Local Alignment Tool (BLAST), Codon Code Aligner and MEGA X respectively. Results A 100% identity of rbcL locus with several other Cyperus species was obtained from BLAST result. The region seems highly conserved among several Cyperus species as variation within this marker locus’s sequence is minimal. However, a G/T variation at a nucleotide position could differentiate the tested samples from 40% of the other data bank species. The phylogenetic tree analysis clustered the 20 samples and the retrieved sequences based on the very few sequence variations without distinctly separatingC. esculentussamples from other Cyperus species. Conclusions These findings showed that rbcL marker could only identify our samples up to genius level. Therefore, other DNA barcoding markers are needed to identify and characteriseC. esculentussince the characterization based on rbcL gene sequences conducted in this work could not identifyC. esculentusup to the species level.

Publisher

Research Square Platform LLC

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