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. 2025 Jan 8;12(1):4.
doi: 10.1038/s41439-024-00308-6.

High-coverage whole-genome sequencing of a Jakun individual from the "Orang Asli" Proto-Malay subtribe from Peninsular Malaysia

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High-coverage whole-genome sequencing of a Jakun individual from the "Orang Asli" Proto-Malay subtribe from Peninsular Malaysia

Wai-Sum Yap et al. Hum Genome Var. .

Abstract

Jakun, a Proto-Malay subtribe from Peninsular Malaysia, is believed to have inhabited the Malay Archipelago during the period of agricultural expansion approximately 4 thousand years ago (kya). However, their genetic structure and population history remain inconclusive. In this study, we report the genome structure of a Jakun female, based on whole-genome sequencing, which yielded an average coverage of 35.97-fold. We identified approximately 3.6 million single-nucleotide variations (SNVs) and 517,784 small insertions/deletions (indels). Of these, 39,916 SNVs were novel (referencing dbSNP151), and 10,167 were nonsynonymous (nsSNVs), spanning 5674 genes. Principal Component Analysis (PCA) revealed that the Jakun genome sequence closely clustered with the genomes of the Cambodians (CAM) and the Metropolitan Malays from Singapore (SG_MAS). The ADMIXTURE analysis further revealed potential admixture from the EA and North Borneo populations, as corroborated by the results from the F3, F4, and TreeMix analyses. Mitochondrial DNA analysis revealed that the Jakun genome carried the N21a haplogroup (estimated to have occurred ~19 kya), which is commonly found among Malays from Malaysia and Indonesia. From the whole-genome sequence data, we identified 825 damaging and deleterious nonsynonymous single-nucleotide polymorphisms (nsSNVs) affecting 720 genes. Some of these variants are associated with age-related macular degeneration, atrial fibrillation, and HDL cholesterol level. Additionally, we located a total of 3310 variants on 32 core adsorption, distribution, metabolism, and elimination (ADME) genes. Of these, 193 variants are listed in PharmGKB, and 21 are nsSNVs. In summary, the genetic structure identified in the Jakun individual could enhance the mapping of genetic variants for disease-based population studies and further our understanding of the human migration history in Southeast Asia.

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Conflict of interest statement

Competing interests: The authors declare no competing interests. Ethics approval and consent to participate: This study was approved by the Research and Ethics Committee of Universiti Teknologi MARA [Ref no: 600-RMI (5/1/6)] and the Department of Orang Asli Development (Jabatan Kemajuan Orang Asli Malaysia, JAKOA) [JHEOA.PP.30.052. Jld 5(17)]. The subject consented to participate in this study.

Figures

Fig. 1
Fig. 1. Geographical map of Peninsular Malaysia.
The sampling location for the Jakun individual used in this study is highlighted in solid red.
Fig. 2
Fig. 2. Principal component analysis (PCA) of the Jakun_Seq individual.
a Global populations; (b) East Asian and Southeast Asian populations; and (c) Southeast Asian populations. The red arrow indicates the Jakun_Seq in this study.
Fig. 3
Fig. 3. Admixture results of the Jakun individual.
a Global populations; (b) East Asian and Southeast Asian populations; and (c) Southeast Asian populations. Each population is represented by a vertical line divided into colored segments that represent membership coefficients in the subgroups.
Fig. 4
Fig. 4. Maximum-likelihood tree generated using TreeMix with 100 bootstraps for Jakun at K = 5.
A migration event was observed from the root of the common ancestor of North Borneo populations to the Jakun, implying a plausible shared common ancestor between the two populations.

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