DNA Barcoding, Phylogenetic Analysis and Secondary Structure Predictions of Nepenthes ampullaria, Nepenthes gracilis and Nepenthes rafflesiana

Author:

Saidon Nur Azreen1,Wagiran Alina1ORCID,Samad Abdul Fatah A.1,Mohd Salleh Faezah1ORCID,Mohamed Farhan2ORCID,Jani Jaeyres3,Linatoc Alona C45

Affiliation:

1. Department of Biosciences, Faculty of Science, Universiti Teknologi Malaysia, Johor Bahru 81310, Johor, Malaysia

2. Media and Games Innovation Centre, Universiti Teknologi Malaysia, Johor Bahru 81310, Johor, Malaysia

3. Borneo Medical and Health Research Center, Faculty of Medicine and Health Sciences, Universiti Malaysia Sabah, Kota Kinabalu 88400, Sabah, Malaysia

4. Faculty of Applied Sciences & Technology, Universiti Tun Hussein Onn Malaysia (UTHM), Hab Pendidikan Tinggi Pagoh, KM1, Jalan Panchor, Muar 84600, Johor, Malaysia

5. College of Forestry and Natural Resources, University of the Philippines Los Banos College, Los Baños 4031, Laguna, Philippines

Abstract

Nepentheceae, the most prominent carnivorous family in the Caryophyllales order, comprises the Nepenthes genus, which has modified leaf trap characteristics. Although most Nepenthes species have unique morphologies, their vegetative stages are identical, making identification based on morphology difficult. DNA barcoding is seen as a potential tool for plant identification, with small DNA segments amplified for species identification. In this study, three barcode loci; ribulose-bisphosphate carboxylase (rbcL), intergenic spacer 1 (ITS1) and intergenic spacer 2 (ITS2) and the usefulness of the ITS1 and ITS2 secondary structure for the molecular identification of Nepenthes species were investigated. An analysis of barcodes was conducted using BLASTn, pairwise genetic distance and diversity, followed by secondary structure prediction. The findings reveal that PCR and sequencing were both 100% successful. The present study showed the successful amplification of all targeted DNA barcodes at different sizes. Among the three barcodes, rbcL was the least efficient as a DNA barcode compared to ITS1 and ITS2. The ITS1 nucleotide analysis revealed that the ITS1 barcode had more variations compared to ITS2. The mean genetic distance (K2P) between them was higher for interspecies compared to intraspecies. The results showed that the DNA barcoding gap existed among Nepenthes species, and differences in the secondary structure distinguish the Nepenthes. The secondary structure generated in this study was found to successfully discriminate between the Nepenthes species, leading to enhanced resolutions.

Funder

Ministry of Higher Education

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Reference46 articles.

1. McPherson, S., and Robinson, A.S. (2012). Field Guide to the Pitcher Plants of Peninsular Malaysia and Indochina, Redfern Natural History.

2. Clarke, C. (1997). Nepenthes of Borneo, Natural History Publications (Borneo).

3. Clarke, C. (2001). Nepenthes of Sumatra and Peninsular Malaysia, Natural History Publications (Borneo).

4. Cheek, M., and Jebb, M. (2001). Flora Malesiana, National Herbarium of the Netherlands.

5. A skeletal revision of nepenthes (Nepenthaceae);Jebb;Blumea J. Plant Taxon. Plant Geogr.,1997

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