» Articles » PMID: 29215087

Mitochondrial DNA Variations in Austronesian-speaking Populations Living in the New Georgia Islands, the Western Province of the Solomon Islands

Overview
Journal J Hum Genet
Specialty Genetics
Date 2017 Dec 8
PMID 29215087
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Modern Austronesian (AN)-speaking Melanesians are considered to be derived from the admixture of indigenous non-Austronesian (NAN)-speaking people and AN-speaking people from Southeast Asia. In this study, we analyzed mitochondrial DNA (mtDNA) variations in the D-loop region for two AN-speaking Melanesian populations (Munda and Kusaghe) and an AN-speaking Micronesian population (Rawaki) in the New Georgia Islands, the Western Province of the Solomon Islands to examine their genetic similarities to AN-speaking Polynesians in Tonga and NAN-speaking Melanesians, Gidra, in Papua New Guinea. The 'Polynesian motif', which is well-characterized mtDNA marker for Polynesians, was frequently observed in Munda and Kusaghe. Of particular interest, haplogroup E1a2 + 16261, which has been rarely observed in the Solomon Islands, accounted for 12.8% in Kusaghe. It has been reported that the haplogroup E1a2 arose in Island Southeast Asia (ISEA) 9400 ± 2850 years ago. Phylogenetic and principle component analyses for 24 Oceanian populations revealed that Munda and Kusaghe populations were genetically close to Tongan population, but not to Gidra. Rawaki population showed no apparent genetic similarities to populations of Tonga and Gidra. Our results suggest that considerable gene flow from AN-speaking populations originated from Southeast Asia to indigenous Melanesians occurred in the New Georgia Islands.

Citing Articles

Admixture and natural selection shaped genomes of an Austronesian-speaking population in the Solomon Islands.

Isshiki M, Naka I, Watanabe Y, Nishida N, Kimura R, Furusawa T Sci Rep. 2020; 10(1):6872.

PMID: 32327716 PMC: 7181741. DOI: 10.1038/s41598-020-62866-3.

References
1.
Weissensteiner H, Pacher D, Kloss-Brandstatter A, Forer L, Specht G, Bandelt H . HaploGrep 2: mitochondrial haplogroup classification in the era of high-throughput sequencing. Nucleic Acids Res. 2016; 44(W1):W58-63. PMC: 4987869. DOI: 10.1093/nar/gkw233. View

2.
Kayser M, Brauer S, Cordaux R, Casto A, Lao O, Zhivotovsky L . Melanesian and Asian origins of Polynesians: mtDNA and Y chromosome gradients across the Pacific. Mol Biol Evol. 2006; 23(11):2234-44. DOI: 10.1093/molbev/msl093. View

3.
Kayser M, Choi Y, van Oven M, Mona S, Brauer S, Trent R . The impact of the Austronesian expansion: evidence from mtDNA and Y chromosome diversity in the Admiralty Islands of Melanesia. Mol Biol Evol. 2008; 25(7):1362-74. DOI: 10.1093/molbev/msn078. View

4.
Saitou N, Nei M . The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol. 1987; 4(4):406-25. DOI: 10.1093/oxfordjournals.molbev.a040454. View

5.
Tamura K, Stecher G, Peterson D, Filipski A, Kumar S . MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Mol Biol Evol. 2013; 30(12):2725-9. PMC: 3840312. DOI: 10.1093/molbev/mst197. View