2017
DOI: 10.1080/23802359.2017.1372709
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The mitogenomes of Gelochelidon nilotica and Sterna hirundo (Charadriiformes, Sternidae) and their phylogenetic implications

Abstract: Gelochelidon nilotica and Sterna hirundo are two sympatric breeding species. The mitogenomes of G. nilotica and S. hirundo are 16,748 bp and 16,707 bp in size. Both two mitogenomes reveal the same gene order and genomic organization to that of typical avian mtDNA. The first conserved blocks with a interrupted poly-C are present in the two species control regions, but not existed in S. albifrons . Seventeen an… Show more

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Cited by 6 publications
(4 citation statements)
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“…2c). In the case of the common tern (Sterna hirundo), the current RefSeq sequence (PCR and Sanger sequencing [46]) was missing a duplication in the CR involving the MT-CYB, MT-TT, MT-TL2, MT-ND6, and MT-TE genes, as well as a substantial fraction of a tandem repeat. In the case of the Indo-Pacific tarpon (Megalops cyprinoides), a~650-bp tandem repeat was represented in the RefSeq reference (long-range PCR and direct Sanger sequencing [47]) for two thirds of its length, and the sequence downstream was completely absent, for~500 bp.…”
Section: Novel Duplications Repeats and Heteroplasmymentioning
confidence: 99%
“…2c). In the case of the common tern (Sterna hirundo), the current RefSeq sequence (PCR and Sanger sequencing [46]) was missing a duplication in the CR involving the MT-CYB, MT-TT, MT-TL2, MT-ND6, and MT-TE genes, as well as a substantial fraction of a tandem repeat. In the case of the Indo-Pacific tarpon (Megalops cyprinoides), a~650-bp tandem repeat was represented in the RefSeq reference (long-range PCR and direct Sanger sequencing [47]) for two thirds of its length, and the sequence downstream was completely absent, for~500 bp.…”
Section: Novel Duplications Repeats and Heteroplasmymentioning
confidence: 99%
“…DNA was extracted using DNeasy Blood and Tissue kit (Quiagen, Hilden Germany) following the manufacturer's protocol. To amplify ~800 bp long fragment of the control region, we designed primers SH-mtCR4F (AACACCCATC-CAACTCGGAA) and SH-mtCR4R (AAT-TTCACTGTCGTTGACGTGT) using the mitogenome sequence from GeneBank (Yang et al 2017). PCR conditions were as follows: 3 min denaturation at 95°C, followed by 40 cycles of 30s at 95°C, 45s of annealing at 52°C, and 45s of elongation at 72°C.…”
Section: Methodsmentioning
confidence: 99%
“…As of now, 47 complete mitochondrial genomes of Charadriiformes birds are available in the GenBank database. Among them, 13 mitogenomes of 11 Laridae species were generated from different geographical regions (Slack et al 2007;Ryu and Hwang 2012;Yang et al 2012Yang et al , 2016Yang et al , 2017Yoon et al 2015;Dong et al 2016;Kim and Park 2016;Anmarkrud and Lifjeld 2017;Skujina et al 2019). The analysis of the complete mitogenomes was also evidenced to characterize various genomic traits within protein-coding genes (PCGs), ribosomal RNA (rRNA), transfer RNA (tRNA), and control region (CR) as well as to detect gene order evolution in birds (Bensch and H€ arlid 2000;Crochet and Desmarais 2000;Ruokonen and Kvist 2002;Pacheco et al 2011).…”
Section: Introductionmentioning
confidence: 99%