Molecular characterization and genetic diversity of Jatropha curcas L. in Costa Rica

Sistema de Estudios de Posgrado, Universidad de Costa Rica, San Pedro, Costa Rica
Escuela de Biología, Universidad de Costa Rica, San Pedro, San José, Costa Rica
Centro de Investigación en Biología Celular y Molecular, Universidad de Costa Rica, San Pedro, San José, Costa Rica
Estación Experimental Fabio Baudrit Moreno, Universidad de Costa Rica, Alajuela, Costa Rica
Programas Agricolas, Ministerio de Agricultura y Ganadería, San José, Costa Rica
Programas Nacionales, Ministerio de Agricultura y Ganaderia, San Jose, Costa Rica
Escuela de Biología, Instituto Tecnológico de Costa Rica, Cartago, Cartago, Costa Rica
Centro de Investigación en Biología Celular y Molecular, Escuela de Tecnología de Alimentos, Centro Nacional en Ciencia y Tecnología de Alimentos, Universidad de Costa Rica, San Pedro, San José, Costa Rica
DOI
10.7287/peerj.preprints.2469v2
Subject Areas
Biodiversity, Molecular Biology, Plant Science
Keywords
Genetic diversity, Jatropha curcas, SCARs markers, EST-SSR, nrDNA-ITS region
Copyright
© 2017 Vásquez-Mayorga et al.
Licence
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ Preprints) and either DOI or URL of the article must be cited.
Cite this article
Vásquez-Mayorga M, Fuchs EJ, Hernández EJ, Herrera F, Hernández J, Moreira IM, Arnáez E, Barboza NM. 2017. Molecular characterization and genetic diversity of Jatropha curcas L. in Costa Rica. PeerJ Preprints 5:e2469v2

Abstract

We estimated the genetic diversity of 50 Jatropha curcas Costa Rican samples using 18 EST-SSR, one G-SSR and nrDNA-ITS markers. We also evaluated the phylogenetic relationships among samples using nuclear ribosomal ITS markers. Non-toxicity was also evaluated using G-SSRs and SCARs markers. A Neighbor-Joining (NJ) tree and a Maximum Likelihood (ML) tree were constructed using SSR markers and ITS sequences, respectively. Heterozygosity was moderate (He = 0.346), but considerable when compared to worldwide values for J. curcas. The PIC (PIC = 0.276) and inbreeding coefficient (f = -0.102) were both low. Clustering was not related to the geographical origin of accessions but Costa Rican J. curcas consistently clustered as a separate group. International accessions clustered independently of collection sites suggesting a lack of genetic structure, probably due to a wide distribution of this crop and ample gene flow. Molecular markers identified only one non-toxic accession (JCCR-24) from Mexico. This work is part of a countrywide effort to characterize the genetic diversity of Jatropha curcas germplasm bank in Costa Rica.

Author Comment

Minor changes has been done as describe here:

1/18 Change to Ileana instead of Ilenana

4/18 Table 1. Change Capulín instead of Capulin and Diquís instead of Diquis

5/18 Include dashes in sentence "and JCITS- 2-R (5´- CCTGGGGTCGCGATGTGAGCGT -3´ )"

5/18 Content instead of content. Please change to capital C

7/18 Insert (JCT27, JcSSR-26 and JCT31). Insert after the word "markers" in text

Answers to specific questions in last page:

Q1 Affiliations checked, they are accurate

Q2 The citation is now correct

Q3 Text provided correspond to titles. We agree the current version.

Supplemental Information

Costa Rica map

Supplementary information (S 1). Map of Costa Rica with sampling sites were Jatropha curcas accessions were collected.

DOI: 10.7287/peerj.preprints.2469v2/supp-1

Raw data from SSR markers

Raw data 1. Results obtained with molecular markers using Powermarker 3.25 software (Liu & Muse, 2005).

DOI: 10.7287/peerj.preprints.2469v2/supp-2

Raw data with resuts from Power marker

Raw data 2. Results obtained with molecular markers using Powermarker 3.25 software (Liu & Muse, 2005).

DOI: 10.7287/peerj.preprints.2469v2/supp-3

Raw data from Power marker

Raw data 3. Results obtained with molecular markers using Powermarker 3.25 software (Liu & Muse, 2005).

DOI: 10.7287/peerj.preprints.2469v2/supp-4

Raw data form power marker

Raw data 4. Results obtained with molecular markers using Powermarker 3.25 software (Liu & Muse, 2005).

DOI: 10.7287/peerj.preprints.2469v2/supp-5

Alignment for ITS sequences

Raw data 5. Alignment for ITS sequences obtained from ITS primers.

DOI: 10.7287/peerj.preprints.2469v2/supp-6