Ana Nantón
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Ana Nantón has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Josefina Méndez
Xenomar Group, Department of Cellular and Molecular Biology, University of A Coruña, A Coruña, Spain
4 shared publications - Jenyfer Fernández-Pérez
Departamento de Bioloxía, Facultade de Ciencias and CICA (Centro de Investigacións Científicas Avanzadas), Universidade da Coruña, A Coruña, Spain
3 shared publications - Miguel Baptista Gaspar
Instituto Português do Mar e da Atmosfera (IPMA, I.P.), Avenida 5 de Outubro s/n, 8700-305 Olhão, Portugal
2 shared publications - Alberto Arias-Pérez
Área de Genética, Facultad de Ciencias del Mar y Ambientales, INMAR, Universidad de Cádiz. 11510 Puerto Real, Cádiz, Spain, Spain
1 shared publication - Elsa Froufe
CIIMAR/CIMAR, LA—Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Matosinhos, Portugal
1 shared publication - Ruth Freire
Departamento de Bioloxía‐Facultade de Ciencias and Centro de Investigacións Científicas Avanzadas (CICA)Universidade da Coruña A Coruña Spain
1 shared publication
Latest Publications
- Open Access
- 26 October 2018
- Published by Springer Nature in BMC Genetics
- Vol. 19 (1) , 97
Sequence characterization of the 5S ribosomal DNA and the internal transcribed spacer (ITS) region in four European Donax species (Bivalvia: Donacidae)
The whole repeat unit of 5S rDNA and the internal transcribed spacer (ITS) of four European Donax species were analysed. After amplifying, cloning and sequencing several 5S and ITS units, their basic features and their variation were described. The phylogenetic usefulness of 5S and ITS sequences in the inference of evolutionary relationships among these wedge clams was also investigated. The length of the 5S repeat presented little variation among species, except D. trunculus that differed from the rest of the Donax species in 170–210 bp. The deduced coding region covered 120 bp, and showed recognizable internal control regions (ICRs) involved in the transcription. The length of non-transcribed spacer region (NTS) ranged from 157 bp to 165 bp in Donax trunculus and from 335 bp to 367 bp in the other three species. The conservation degree of transcriptional regulatory regions was analysed revealing a conserved TATA-like box in the upstream region. Regarding ITS sequences, the four Donax species showed slight size differences among clones due to the variation occurring in the ITS1 and ITS2, except Donax variegatus did not display size differences in the ITS2. The total length of the ITS sequence ranged between 814 and 1014 bp. Resulting phylogenetic trees display that the two ribosomal DNA regions provide well-resolved phylogenies where the four European Donax species form a single clade receiving high support in nodes. The topology obtained with 5S sequences was in agreement with Donax evolutionary relationships inferred from several sequences of different nature in previous studies. This is not only a basic research work, where new data and new knowledge is provided about Donax species, but also have allowed the authentication of these wedge clams and offers future applications to provide other genetic resources.
- 26 October 2018
- Published by Springer Nature in BMC Genetics
- Vol. 19 (1) , 97
Open AccessSequence characterization of the 5S ribosomal DNA and the internal transcribed spacer (ITS) region in four European Donax species (Bivalvia: Donacidae)
The whole repeat unit of 5S rDNA and the internal transcribed spacer (ITS) of four European Donax species were analysed. After amplifying, cloning and sequencing several 5S and ITS units, their basic features and their variation were described. The phylogenetic usefulness of 5S and ITS sequences in the inference of evolutionary relationships among these wedge clams was also investigated. The length of the 5S repeat presented little variation among species, except D. trunculus that differed from the rest of the Donax species in 170–210 bp. The deduced coding region covered 120 bp, and showed recognizable internal control regions (ICRs) involved in the transcription. The length of non-transcribed spacer region (NTS) ranged from 157 bp to 165 bp in Donax trunculus and from 335 bp to 367 bp in the other three species. The conservation degree of transcriptional regulatory regions was analysed revealing a conserved TATA-like box in the upstream region. Regarding ITS sequences, the four Donax species showed slight size differences among clones due to the variation occurring in the ITS1 and ITS2, except Donax variegatus did not display size differences in the ITS2. The total length of the ITS sequence ranged between 814 and 1014 bp. Resulting phylogenetic trees display that the two ribosomal DNA regions provide well-resolved phylogenies where the four European Donax species form a single clade receiving high support in nodes. The topology obtained with 5S sequences was in agreement with Donax evolutionary relationships inferred from several sequences of different nature in previous studies. This is not only a basic research work, where new data and new knowledge is provided about Donax species, but also have allowed the authentication of these wedge clams and offers future applications to provide other genetic resources.
- 17 May 2018
- Published by Springer Nature in European Food Research and Technology
- Vol. 244 (10) , 1815-1820
An alternative method for rapid and specific authentication of four European Donax species, including D. trunculus a commercially-important bivalve
- 17 May 2018
- Published by Springer Nature in European Food Research and Technology
- Vol. 244 (10) , 1815-1820
An alternative method for rapid and specific authentication of four European Donax species, including D. trunculus a commercially-important bivalve
- 23 January 2015
- Published by Springer Nature in European Food Research and Technology
- Vol. 240 (6) , 1129-1133
Identification of four Donax species by PCR–RFLP analysis of cytochrome c oxidase subunit I (COI)
- 23 January 2015
- Published by Springer Nature in European Food Research and Technology
- Vol. 240 (6) , 1129-1133
Identification of four Donax species by PCR–RFLP analysis of cytochrome c oxidase subunit I (COI)