Colección SciELO Chile

Departamento Gestión de Conocimiento, Monitoreo y Prospección
Consultas o comentarios: productividad@anid.cl
Búsqueda Publicación
Búsqueda por Tema Título, Abstract y Keywords



A first genomic portrait of the deep-water azooxanthellate reef-building coral Madracis myriaster: genome size, repetitive elements, nuclear RNA gene operon, mitochondrial genome, and phylogenetic placement in the family Pocilloporidae
Indexado
Scopus SCOPUS_ID:85173057093
DOI 10.1007/S00338-023-02419-Y
Año 2023
Tipo

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



The coral Madracis myriaster is one of the most important reef builders in deep-water habitats of the Caribbean Sea, offering refuge to numerous species of fish and invertebrates. In this study, we developed genomic resources for M. myriaster. Using a low-coverage short read sequencing strategy, this study estimated the genome size, repetitive genome content, annotated and quantified repetitive elements, assembled the 45S rRNA DNA operon, and characterized in detail the mitochondrial genome of M. myriaster. The haploid genome size estimated using a k-mer strategy was 615–697 Mbp, which is within the range reported for scleractinian corals. Repetitive genome content estimates using different word sizes (= k-mers) indicated that 53–65% of the genome of M. myriaster comprised repetitive elements. A relatively large number of the discovered repetitive elements could not be annotated. Taking into account only annotated repetitive elements, the most common were classified as Satellite DNA which were more abundant than Class I-LINE, Class I—Penelope, and Class II (DNA transposons)—Subclass 2 Maverick mobile elements. Less abundant repeat element families included Class I-LTR Ty3 retrotransposons, Class II-Subclass 2-Helitron mobile elements, Class I-LTR-Bel-Pao, and Class I-DIRS mobile elements. The nuclear ribosomal operon of M. myriaster was assembled into a single contig that contains, in the following order: a 5′ ETS [length = 1200 bp (partially assembled)], ssrDNA (1800 bp), ITS1 (233 bp), 5.8S rDNA (158 bp), ITS2 (204 bp), lsrDNA (3616 bp), and 3′ ETS [827 bp (partial sequence)]. The mitochondrial genome of M. myriaster is 17,044 bp long and encodes 13 protein-coding genes, 2 transfer RNAs, and two ribosomal genes. Based on protein-coding genes, the phylogenetic position of M. myriaster was examined. These new genomic resources are of utmost relevance to improve the understanding of the biology of M. myriaster and for the development of conservation plans in this reef-forming deep-water coral.

Revista



Revista ISSN
Coral Reefs 0722-4028

Métricas Externas



PlumX Altmetric Dimensions

Muestra métricas de impacto externas asociadas a la publicación. Para mayor detalle:

Disciplinas de Investigación



WOS
Marine & Freshwater Biology
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

Muestra la distribución de disciplinas para esta publicación.

Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



Muestra la distribución de colaboración, tanto nacional como extranjera, generada en esta publicación.


Autores - Afiliación



Ord. Autor Género Institución - País
1 Tucker, Joshua - Clemson University - Estados Unidos
2 Barrios, Lina M. - Biodiversity & Development - Solutions for Sustainability - Colombia
University of Plymouth - Reino Unido
3 Preziosi, Richard - University of Plymouth - Reino Unido
4 BAEZA-MIGUELES, JUAN ANTONIO Hombre Clemson University - Estados Unidos
Universidad Católica del Norte - Chile
Smithsonian Marine Station - Estados Unidos

Muestra la afiliación y género (detectado) para los co-autores de la publicación.

Financiamiento



Fuente
California Department of Fish and Game
Bundesministerium für Bildung und Forschung
Collaborative Research Centre 992 Medical Epigenetics

Muestra la fuente de financiamiento declarada en la publicación.

Agradecimientos



Agradecimiento
J.A.B thanks Vincent P. Richards for bioinformatics support. The Galaxy server that was used for some calculations is in part funded by Collaborative Research Centre 992 Medical Epigenetics (DFG grant SFB 992/1 2012) and German Federal Ministry of Education and Research (BMBF grants 031 A538A/A538C RBC, 031L0101B/031L0101C de.NBI-epi, 031L0106 de.STAIR (de.NBI)). The authors thank Diana C. Ballesteros for permission to use her photographs.

Muestra la fuente de financiamiento declarada en la publicación.