The Philippines exhibits a rich diversity of people, languages, and culture, including so-called ‘Negrito’ groups that have for long fascinated anthropologists, yet little is known about their genetic diversity. We report here, a survey of Y-chromosome variation in 390 individuals from 16 Filipino ethnolinguistic groups, including six Negrito groups, from across the archipelago. We find extreme diversity in the Y-chromosome lineages of Filipino groups with heterogeneity seen in both Negrito and non-Negrito groups, which does not support a simple dichotomy of Filipino groups as Negrito vs non-Negrito. Filipino non-recombining region of the human Y chromosome lineages reflect a chronology that extends from after the initial colonization of the Asia-Pacific region, to the time frame of the Austronesian expansion. Filipino groups appear to have diverse genetic affinities with different populations in the Asia-Pacific region. In particular, some Negrito groups are associated with indigenous Australians, with a potential time for the association ranging from the initial colonization of the region to more recent (after colonization) times. Overall, our results indicate extensive heterogeneity contributing to a complex genetic history for Filipino groups, with varying roles for migrations from outside the Philippines, genetic drift, and admixture among neighboring groups.
The Philippines figures prominently in two significant demographic events in the Asia-Pacific region. The first was the initial colonization of Sunda and Sahul around 40–50 thousand years ago (KYA)1 to which the human fossil remains from Tabon Cave, Palawan in the Philippines, with estimated ages ranging from 14 to 58 thousand years (KY),2 may be associated.3 The second was the Austronesian expansion, which is proposed to have originated in Taiwan around 5–6 KYA and spread first to the Philippines before continuing to Southeast Asia, Near and Remote Oceania, and Madagascar.4 The impact of the Austronesian expansion is evidenced by the fact that all Philippine languages today are Austronesian.5 In addition, a popularly accepted ‘waves of migration theory’ suggests that the origins and diversity of people in the Philippines was the result of several migrations into the archipelago during the periods of low water levels, when there existed land bridges with the Sunda shelf via Palawan and the Sulu Archipelago, and with Celebes via Mindanao.6, 7
Currently, over 170 Filipino ethnolinguistic (FE) groups are recognized on the basis of language and culture.5 Of these FE groups, anthropologists have traditionally been most interested in those with short stature, frizzy hair, and dark skin color, historically defined as ‘Negrito’ groups.8 There are more than 20 FE Negrito (FEN) groups in the Philippines.5 It has been proposed that Negrito groups represent a separate migration out of Africa.9 Although all FEN groups currently speak Austronesian languages, it has been proposed that they originally spoke non-Austronesian languages, which were subsequently replaced by Austronesian languages.10 This view, along with their physical features and hunter-gatherer mode of subsistence, has resulted in the historical depiction of the FEN groups as the aboriginal, first occupants of the archipelago, and as such, the popular distinction of FEN vs non-Negrito FE (FEnN) groups has been perpetuated.7
To date, no comprehensive genetic diversity study of FE groups has been presented. A mitochondrial DNA (mtDNA) study on Philippine populations showed further support for the ‘out of Taiwan’ hypothesis for the Austronesian expansion, as well as identifying rare mtDNA haplotypes; however, samples were not from specific FE groups, but from urban populations, and from Filipinos living in Taiwan.11 Early studies have inferred genetic differences between some FEN groups (the Aeta of Bataan, Aeta of Zambales and the Mamanwa)12, 13 and possible affinities with populations, such as indigenous Australians and Papuan groups.12 A recent genome-wide study on Asian populations included six FEN groups, but only one other FEnN group, and three urban populations.14
We, therefore, report a survey of genetic variation in the non-recombining region of the human Y chromosome (NRY) of 16 FE groups (six FEN and 10 FEnN groups). Our results indicate that, a simple division of FEN vs FEnN groups is not supported by the NRY evidence. Instead, FE groups, in general, demonstrate extensive heterogeneity and diverse genetic affinities with their geographic neighbors, suggesting a complex history, reflecting varying roles of migration from outside the Philippines, genetic drift, and admixture among FE groups and with other Asia-Pacific groups.
Materials and methods
DNA samples were collected from 390 unrelated males from 16 FE groups, representing eight Philippine geographical regions and three language groupings (Figure 1, Supplementary Text). Population sampling was conducted independently by the DNA Analysis Laboratory, Natural Sciences Research Institute, University of the Philippines (UP-NSRI-DAL) and the Max Planck Institute for Evolutionary Anthropology (MPI-EVA), and the sample collections of both institutions were combined to form the data set in this study (Supplementary Text). Human population sampling procedures followed the guidelines outlined by the Philippine National Bioethics Committee on Scientific Research, the National Commission on Indigenous Peoples (NCIP) and the MPI-EVA. Free, prior and informed consent for sample collection was obtained at the level of the community and the individual.
DNA samples were extracted from whole-blood or oral samples (buccal swabs and/or saliva) using commercially available (FTA Gene Guard system (Whatman Inc., Springfield Mill, Maidstone, Kent, UK), QIAamp DNA Blood Mini kit (QIAGEN Inc., Valencia, CA, USA)) and published protocols.15 DNA samples were typed for 48 NRY binary markers (Y-SNPs) (Supplementary Figure 1). A set of Y-SNP multiplexes previously described16, 17 were typed using the ABI Prism SNaPshot multiplex kit (Applied Biosystems, Foster, CA, USA) (Supplementary Text, Supplementary Table 1). Another set of multiplexes were typed using a single-base extension (SBE) assay described elsewhere18 (Supplementary Text, Supplementary Table 1). Y-chromosome microsatellite/short tandem repeat (Y-STR) markers were typed using the PowerPlex Y system (Promega Corporation, Madison, WI, USA) following manufacturer's instructions (Supplementary Text). For Y-SNP haplogroup nomenclature, the capital letter (major clade) – terminal mutation (NRY binary marker) naming system19 was adopted.
For population comparisons, a reference data set was assembled from previously published works,20, 21, 22, 23, 24 composed of 1756 males from 60 groups representing five Asia-Pacific regions (Figure 1). Reference data set population codes and measures to ensure compatibility with the Filipino data set are discussed in Supplementary Text.
The Arlequin software version 3.1125 (http://cmpg.unibe.ch/software/arlequin3) was used to calculate genetic diversity indices: Haplogroup diversity (HgD), Haplotype diversity (HtD), haplotype mean pairwise difference (MPD) and Analysis Of Molecular Variance (AMOVA). AMOVA analyses were performed using different groupings (geography, language classification, FEN vs FenN, and all groups collectively (Figure 1)). Mann–Whitney U tests and correspondence analyses (CA) were performed using the STATISTICA software package.26 Network analyses were performed using Network version 4.510 and Network Publisher version 220.127.116.11 (http://fluxus-engineering.com). The BATWING program27 (http://www.mas.ncl.ac.uk/~nijw/) was used to estimate haplogroup coalescent times (Time since the Most Recent Common Ancestor –(TMRCA)). The IM program28 (http://genfaculty.rutgers.edu/hey/software) was used to estimate divergence times and migration rates. Details for Network analyses, estimation of coalescent times, divergence times, and migration rates are given in Supplementary Text.
NRY diversity and genetic relationships of Filipino ethnolinguistic groups
Eleven Y-SNP haplogroups were observed among 390 unrelated males from 16 FE groups (Figure 1). Five major haplogroups (C-RPS4Y, K-M9, O-M119, O-M110, and O-M122) had frequencies >5% and were present among a greater number of FE groups than minor haplogroups (NO-M214, O-M175, O-M7, O-M95, O-M134, and P-M74) with <5% frequency (Table 1, Figure 1). In general, there is a patchy distribution of all haplogroups (Figure 1), such that even the most frequent haplogroup O-M119, observed among northern, central, and southern FE groups, was present in only 12 out of 16 FE groups. This distribution may be the result of genetic drift, which is detectable with the NRY because of its low effective population size.
For genetic diversity indices (Table 2), HgD ranged from 0 (in the Aeta of Zambales and the Tadyawan, who were fixed for haplogroups K-M9 and O-M110, respectively) to 0.83. Y-STR diversity indices such as HtD also ranged widely, from 0.59 (in the Tadyawan) to 0.97 (Ivatan, CAR, and Surigaonon), and MPD ranged from 1.40 (again in the Tadyawan) to 4.63 (Agta). Extremely low HgD values were observed for some FEN (Aeta of Zambales and Bataan) and FEnN groups, (Bugkalot, Tadyawan, and Tawbuid) further suggesting genetic drift owing to small population sizes. The genetic diversity indices of FEN groups did not significantly differ from FEnN groups, based on Mann–Whitney U tests (HgD: Z=0.52, P=0.61; HtD: Z=−0.32, P=0.75; MPD: Z=1.10, P=0.27), implying no distinction between FEN and FEnN groups based on NRY diversity.
AMOVA analyses showed extensive heterogeneity among FE groups, among FEN groups, and among FEnN groups, with only about 70% of the variation observed within populations in each comparison (Table 3). Only a geographic grouping resulted in a slightly larger difference among groups than among populations within groups. Furthermore, the grouping of FEN vs FEnN also provided a poor description of genetic structure, consistent with the absence of a significant difference between FEN and FEnN diversity indices.
CA based on Y-SNP haplogroup frequencies were used to visualize the genetic relationships of 14 Filipino groups (with samples sizes >10) in association with the distribution of Y-SNP haplogroups. The CA plot (Figure 2) showed three clusters of FE groups: one consisting of the Aeta of Zambales, Aeta of Bataan, and Hanunuo, associated with haplogroup K-M9; one consisting of the Ati, Kalangoya, Tawbuid, and Tadyawan, associated with haplogroups O-M7, O-M110, and O-M134; and the third consisting of the remaining FE groups and haplogroups. There was no tendency for FEN groups to cluster together as they were distributed in all three clusters. There was also no tendency for the three clusters of FE groups to reflect geographic relationships, with the exception of the three southern groups (Surigaonon, Manobo, and Mamanwa), all from northern Mindanao, that cluster together.
Network (Figure 3) and haplotype sharing analyses (Supplementary Figure 2) showed that haplotypes in major haplogroups O-M119, O-M110, and O-M122 were shared among 14 FE groups, regardless of geographic proximity. In contrast, the shared haplotypes in haplogroups C-RPS4Y and KM9 were distributed among nine FE groups, and for the most part tended to involve groups that are geographically close. These patterns seem to reflect different histories for these haplogroups and suggest that C-RPS4Y and K-M9 are likely to be older, while O-M119, O-M110, and O-M122 would have spread more recently. TMRCA estimates and their credible intervals (CI) were consistent with C-RPS4Y (13 245; CI: 7824–20 644) and K-M9 (13 608; CI: 9225–19 709) being older than O-M119 (7299; CI: 5046–10 204), O-M110 (4167; CI: 2837–5898), and O-M122 (6223; CI: 4151-8886).
Genetic affinities of Filipino ethnolinguistic groups
The FE group data set was compared with a reference data set composed of 1756 males from 60 groups across the Asia-Pacific region.20, 21, 22, 23, 24 Figure 1 shows the distribution of shared Y-SNP haplogroups among FE groups and the reference data set. AMOVA results (Table 3) show that the heterogeneity of FE groups were comparable to or exceeded the heterogeneity of the other regions in the reference data set. A CA plot (Figure 4) shows that FE groups have different affinities. The major O haplogroups appear to influence the association of the majority of FE groups with East Asian and Southeast Asian groups and, to a lesser extent, with Melanesian and Polynesian groups. Haplogroups C-RPS4Y and K-M9, drive the association of several FEN groups (Aetas, Ati, and Agta) and the Hanunuo with Southeast Asian and Australian groups. For the major O haplogroups, O-M119, O-M110, and O-M122, Y-STR diversity indices (HtD and MPD) (Supplementary Table 3) were similar for the FE, East, and Southeast Asian groups. Network (Figure 3) and haplotype sharing (Supplementary Table 4) analyses for these three haplogroups showed haplotype sharing between FE groups and all Asia-Pacific groups, with the exception of haplogroup O-M119, for which FE groups shared haplotypes only with East Asia and Southeast Asia. For haplogroup C-RPS4Y, network analysis (Figure 3) showed that FEnN (Ivatan, Manobo, and Surigaonon) and FEN (Ati and Mamanwa) haplotypes were associated with Southeast Asian haplotypes on one branch; while on another, FEN haplotypes (one Ati and all Agta C-RPS4Y haplotypes) were associated with indigenous Australians from Arnhem Land, one Fijian, and several Southeast Asians. This implies two different origins of haplogroup C-RPS4Y in FE groups, one associated with Southeast Asians, and another providing a possible signal of a genetic link between FEN groups (in particular, the Agta, who have the highest frequency of C-RPS4Y among FE groups) and indigenous Australians. It should be noted that the indigenous Australian groups in the reference data set possess, at high frequency, a unique DYS390.1 deletion on the background of haplogroup C-RPS4Y,20 as such these samples were excluded from the C-RPS4Y analysis. The DYS390.1 deletion has been associated with DYS390 allele lengths ranging from 18 to 22 repeats and so far is specific to Australians.20, 24, 29 Several FE groups (Ivatan, Agta, Ati, Surigaonon, Mamanwa, and Manobo) have C-RPS4Y/DYS390 allele lengths within this range (Supplementary Table 2). Although sequence analysis would be required to definitely rule out the DYS390.1 deletion in these individuals, network analysis does not show any association between these FE group haplotypes and the Australian DYS390.1 haplotypes (Supplementary Figure 3). With only three C-RPS4Y haplotypes shared (two among FE groups and one between FE and Southeast Asians) (Figure 3 and Supplementary Table 4), these NRY links between FE, Southeast Asian, and Australian groups are likely to be old. Haplogroup K-M9 was shared between FE groups and different Asia-Pacific regions; but within K-M9, different affinities of FE groups were observed, as seen on different branches of the K-M9 network (Figure 3, b1-b7). FEN (Iraya and Mamanwa) and FEnN (Maranao and Manobo) haplotypes clustered with Southeast Asian and Melanesian haplotypes on b1 and b2. FEnN (Surigaonon and Manobo) haplotypes clustered with Southeast Asian, Melanesian, and Fijian haplotypes on b3. All Ati (FEN) haplotypes were clustered with one Hanunuo (FEnN) haplotype on b4. FEN (two Aeta groups and the Agta) haplotypes were associated with Hanunuo (FEnN) and Southeast Asian haplotypes on b5. FEN (two Aeta groups) haplotypes were associated with one Polynesian, one Fijian, one Melanesian, and six Australian haplotypes on b6. Only FEN (two Aeta groups and the Agta) haplotypes were clustered on b7. Overall, results of FE group-reference data set comparisons for the major O haplogroups, C-RPS4Y, and K-M9 showed the diverse genetic affinities of FE groups. These comparisons also showed support for the observed genetic differences (based on genetic diversity, AMOVA, and CA) among all FE groups.
Negrito – indigenous Australian association: ancient divergence or recent contact?
As there seem to be signals of genetic links between several FEN groups (Aeta-Bataan, Aeta-Zambales, and Agta) and indigenous Australians (Arnhem Land and Great Sandy Desert) (Figure 3: C-RPS4Y and K-M9; Figure 4), divergence times and migration rates between these groups were estimated through pairwise, simulation-based analyses using the IM program.28 Divergence time estimates ranged from 14 549 to 19 799 Y (CI: 4939–75 059), although gene flow was detected from the Arnhem Land Australians to the Aeta of Bataan and the Agta, and from the Great Sandy Desert Australians to the Agta (Table 4 and Supplementary Figure 4). Point estimates indicate divergence times of about 15–20 KYA, after the initial colonization of the Asia-Pacific region around 40–50 KYA,1 though CI values overlap with the initial colonization time period. Time estimates, therefore, do not distinguish between ancient vs more recent divergence between the ancestors of FEN and indigenous Australian groups.
Our analyses revealed several attributes of FE group NRY lineages, namely: extensive heterogeneity, signatures of old and recent periods, and diverse affinities. Heterogeneity is seen in FEN groups, who show an old substrate (haplogroups C-RPS4Y and K-M9) suggesting ancient shared ancestry. Similarities in physical features and mode of subsistence of FEN groups have been the main, if not the only (anthropological), support for the inference of common ancestry.30 Haplogroups K-M9 and C-RPS4Y in this study provide genetic support for the common ancestry of FEN groups. FEN groups also share haplogroups with FEnN groups (ie, Mamanwa with Manobos and Surigaonons; Aeta with Hanunuo), but rather than ancient shared ancestry, gene flow between FEN and FEnN groups has been inferred by early anthropological studies.30 Heterogeneity among FEnN groups is best exemplified by the Hanunuo, Tadyawan, Tawbuid, and Iraya. Historically grouped and called ‘Mangyan’ (with the Iraya also considered a FEN group because of physical features), these groups showed distinct NRY lineages despite their geographical proximity on the island of Mindoro; this may reflect differing cultural practices and language barriers between these groups.30 Owing to readily distinguishable physical features that may be the result of adaptation to their environment,31 confounded by historical and social circumstances, a general grouping of FE groups into FEN and FEnN has been perpetuated.7 However, we find that from a NRY perspective, the extensive heterogeneity of FE groups, influenced by drift and admixture, does not support a simple distinction between FEN and FEnN groups.
Summarized recently, haplogroups C-RPS4Y and K-M9, represent founding lineages in the Asia-Pacific region, while O-M119, O-M110, and O-M122 are associated with the Austronesian expansion.32 The phylogeographic analyses of C-RPS4Y and K-M9 in FE groups suggest that these are old NRY lineages. TMRCA estimates for C-RPS4Y (13 245; CI: 7824–20 644) and K-M9 (13 608; CI: 9225–19 709) also reflect a late Paleolithic timeline and overlap with the ages (14–58 KY) of upper Pleistocene human remains from Tabon Cave, Palawan, Philippines.2 TMRCA estimates for O-M119 (7299; CI: 5046–10 204), O-M110 (4167; CI: 2837–5898), and O-M122 (6223; CI: 4151–8886) in FE groups do overlap with the Austronesian expansion time (5–6 KY).4 In association with the Austronesian expansion, these haplogroups are presumed to have reached the Philippines via Taiwan. However, restricted to the reference data set in this study, only O-M110 has a clear Taiwan-specific origin.23 An alternative scenario was suggested for O-M122, involving expansion from East Asia to Southeast Asia and on to Melanesia.33 O-M122 was found only among central and southern FE groups with significant frequency differences among northern, central, and southern groups (χ2 test; P=0.000029). O-M122 is one of several NRY haplogroups whose diversity has been affected by drift,34 which could explain the absence of O-M122 in northern FE groups. However, a southern entry point into the Philippines could also explain our results. The FE group data for the major O-haplogroups simply suggests that they expanded into the Philippines, either from Taiwan or elsewhere in East Asia, in association with the Austronesian expansion. Overall, this study presents genetic evidence for the settlement of NRY lineages in the Philippines within a time frame after the initial colonization (after 40–50 KYA) of the Asia-Pacific region, extending into the time frame of the Austronesian expansion.
Recently, analysis of about 50 000 SNPs in a wide variety of Asian populations, including several FEN groups, found no clear-cut genetic distinction between FEN and FEnN groups, and concluded that, FEN and FEnN groups were part of the same wave of migration.14 This conclusion seems at odds with both the NRY data, which indicate an earlier presence of haplogroups C-RPS4Y and K-M9 in the Philippines that is associated with FEN groups, and with mtDNA data indicating novel and ancient mtDNA lineages in a FEN group (E Gunnarsdottir and M Stoneking, unpublished data). A possible reconciliation of the genome-wide SNP data with the uniparental marker data is, if the ancestors of FEN groups were isolated from the ancestors of FEnN groups (either as a separate migration or as part of the same migration), but then in recent times FEN groups have experienced substantial, primarily male-mediated admixture with FEnN groups.35 Such substantial admixture, documented in the NRY data as discussed above, could account for the genome-wide SNP data.14
Another interesting finding was the link between C-RPS4Y and K-M9 haplotypes of some FEN groups and indigenous Australians. An early study on FEN groups, using immunoglobulin G genetic markers, inferred a possible ancient link with northeastern indigenous Australians.12 With information only from the NRY, our demographic inference yielded broad divergence time estimates, but with inferred gene flow that seem to run counter to the commonly-held view that there was little contact between Australia and the rest of the world after initial colonization.36 However, given the broad divergence time estimates, as well as the ancient associations inferred from network and haplotype sharing analyses, the inferred gene flow between FEN groups and indigenous Australians need not necessarily imply direct contact between these groups. An alternative possibility is that, gene flow from Australia to the Philippines was only via neighboring populations, in a ‘stepping-stone’ manner. Data from additional loci would be needed to confirm this apparent signal of more recent gene flow involving FEN and indigenous Australian groups.
Our study provides a number of important insights into the genetic history of Filipinos. First, there is extensive diversity in the NRY lineages of FE groups. In general, a simple dichotomy of Negrito vs non-Negrito is not supported by Filipino NRY data. Second, Filipino NRY lineages reflect a chronology and thus, a history that extends from after the initial colonization of the Asia-Pacific region, into the time frame of the Austronesian expansion. Third, the diverse NRY genetic affinities of Filipinos can also be associated with the Austronesian expansion, with older affinities reflecting demographic scenarios after the initial colonization of the Asia-Pacific region, including the possible divergence and subsequent gene flow between some Negrito groups and indigenous Australians. Although the Y-chromosome is a powerful tool for studying demographic events and population history, and has yielded some important new insights in the present study, it is still a single genetic locus. To obtain more accurate estimates of demographic parameters, to verify genetic associations, and to further characterize Filipino genetic diversity, genetic studies from other loci are needed.
O’Connell JF, Allen J : Dating the colonization of Sahul (Pleistocene Australia–New Guinea): a review of recent research. J Arch Sci 2004; 31: 835–853.
Détroit F, Dizon E, Falguères C, Hameau S, Ronquillo W, Sémah F : Upper Pleistocene Homo sapiens from the Tabon cave (Palawan, The Philippines): description and dating of new discoveries. C R Palevol 2004; 3: 705–712.
Barker G, Barton H, Bird M et al: The ‘human revolution’ in lowland tropical Southeast Asia: the antiquity and behavior of anatomically modern humans at Niah Cave (Sarawak, Borneo). J Hum Evol 2007; 52: 243–261.
Gray RD, Drummond AJ, Greenhill SJ : Language Phylogenies Reveal Expansion Pulses and Pauses in Pacific Settlement. Science 2009; 323: 479–483.
Gordon Jr RG . (ed).: Ethnologue: Languages of the World, 15th edn. Dallas, Tex: SIL International. Online version: http://www.ethnologue.com/, 2005.
Scott WH : Prehispanic Source Materials For the Study of Philippine History. Quezon City, Philippines: New Day Publishers, 1984.
Jocano FL : Anthropology of the Filipino People I: Philippine Prehistory, Rediscovering Precolonial Heritage. Diliman, Quezon City, Philippines: PUNLAD Research House, Inc., 1998.
Bean RB : Types of Negritos in the Philippines. Am Anthro 1910; 12: 220–236.
Kashyap VK, Sitalaximi T, Sarkar BN, Trivedi R : Molecular relatedness of the aboriginal groups of Andaman and Nicobar Islands with similar ethnic populations. Int J Hum Genet 2003; 3: 5–11.
Reid LA : Unravelling the linguistic histories of Philippine Negritos; in Dutton T, Tyron DT (eds): Language Contact and Change in the Austronesian World. Berlin, Germany: Mouton de Gruyter, 1994, pp 443–475.
Tabbada KA, Trejaut J, Loo J-H et al: Philippine mitochondrial DNA diversity: A populated viaduct between Taiwan and Indonesia? Mol Biol Evol 2010; 27: 21–31.
Matsumoto H, Miyazaki T, Omoto K et al: Population Genetic Studies of the Philippine Negritos II Gm and Km Allotypes of Three Population Groups. Am J Hum Genet 1979; 31: 70–76.
Omoto K, Ueda S, Goriki K, Takahashi N, Misawa S, Pagaran IG : Population Genetic Studies of the Philippine Negritos. III. Identification of the Carbonic Anhydrase-1 Variant with CA1 Guam. Am J Hum Genet 1981; 33: 105–111.
The HUGO Pan-Asian SNP Consortium: Mapping Human Genetic Diversity in Asia. Science 2009; 326: 1541–1545.
Salvador JM, De Ungria MCA : Isolation of DNA from saliva of betel quid chewers using treated cards. J Forensic Sci 2003; 48: 794–797.
Paracchini S, Arredi B, Chalk R, Tyler-Smith C : Hierarchical high-throughput SNP genotyping of the human Y-chromosome using MALDI-TOF mass spectrometry. Nucleic Acids Res 2002; 30: e27 21–26.
Hurles ME, Sykes BC, Jobling MA, Forster P : The dual origin of the Malagasy in island Southeast Asia and East Africa: Evidence from maternal and paternal lineages. Am J Hum Genet 2005; 76: 894–901.
Hughes DA, Tang K, Strotmann R et al: Parallel Selection on TRPV6 in Human Populations. PLoS ONE 2008; 3: e1686 1681–1613.
Karafet TM, Mendez FL, Meilerman MB, Underhill PA, Zegura SL, Hammer MF : New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree. Genome Res 2008; 18: 830–838.
Kayser M, Brauer S, Weiss G, Schiefenhövel W, Underhill PA, Stoneking M : Independent Histories of Human Y Chromosomes from Melanesia and Australia. Am J Hum Genet 2001; 68: 173–190.
Kayser M, Brauer S, Weiss G et al: Reduced Y-chromosome, but not mitochondrial DNA, diversity in human populations from West New Guinea. Am J Hum Genet 2003; 72: 281–302.
Kayser M, Brauer S, Cordaux R et al: Melanesian and Asian Origins of Polynesians: mtDNA and Y Chromosome Gradients Across the Pacific. Mol Biol Evol 2006; 23: 2234–2244.
Kayser M, Choi Y, van Oven M et al: The Impact of the Austronesian Expansion: Evidence from mtDNA and Y Chromosome Diversity in the Admiralty Islands of Melanesia. Mol Biol Evol 2008; 25: 1362–1374.
Mona S, Grunz KE, Brauer S et al: Genetic Admixture History of Eastern Indonesia as Revealed by Y-Chromosome and Mitochondrial DNA Analysis. Mol Biol Evol 2009; 26: 1865–1877.
Excoffier L, Laval G, Schneider S : Arlequin ver. 3.0: An integrated software package for population genetics data analysis. Evol Bioinform Online 2005; 1: 47–50.
StatSoft, Inc: STATISTICA (data analysis software system), version 8.0, 2008, www.statsoft.com.
Wilson IJ, Weale ME, Balding DJ : Inferences from DNA data: population histories, evolutionary processes and forensic match probabilities. J R Stat Soc Ser A 2003; 166: 155–201.
Hey J, Nielsen R : Multilocus methods for estimating population sizes, migration rates and divergence time, with applications to the divergence of Drosophila pseudoobscura and D. perimilis. Genetics 2004; 167: 747–760.
Forster P, Kayser M, Meyer E et al: Phylogenetic Resolution of Complex Mutational Features at Y-STR DYS390 in Aboriginal Australians and Papuans. Mol Biol Evol 1998; 15: 1108–1114.
Lebar FM (ed.): Ethnic Groups of Insular Southeast Asia Volume 2: Philippines and Formosa. New Haven, USA: Human Relations Area Files Press, 1975.
Perry GH, Dominy NJ : Evolution of the human pygmy phenotype. Trends Ecol Evol 2009; 24: 220–225.
Karafet TM, Hallmark B, Cox MP et al: Major East-West Division Underlies Y Chromosome Stratification Across Indonesia MBE Advance Access published on March 5, 2010. doi:10.1093/molbev/msq063.
Kayser M, Brauer S, Weiss G et al: Melanesian origin of Polynesian Y chromosomes. Curr Biol 2000; 10: 1237–1246.
Chiaroni J, Underhill PA, Cavalli-Sforza LL : Y chromosome diversity, human expansion, drift, and cultural evolution. PNAS 2009; 106: 20174–20179.
Stoneking M, Delfin F : The Human Genetic History of East Asia: Weaving a Complex Tapestry. Curr Biol 2010; 20: R188–R193.
Pardoe C : Becoming Australian: evolutionary processes and biological variation from ancient to modern times. Before Farming [online version] 2006; 2006/1 article 4: 1–21.
We gratefully acknowledge all participants for kindly providing samples for this study and all individuals, institutions and organizations for their assistance in the population sampling process, including all funding organizations that supported this study (see Supplementary Text). We acknowledge the support provided by Miriam Dalet, Minerva Sagum, Michelle Music Tan, Nota Magno, Laarni Carpina, Liza Faustino and Alma Ferrer (UP-NSRI-DAL), Dr Victor Paz (UP Archeological Studies Program) Dr Francisco Datar (UP Anthropology), Dr Sabino Padilla (UP Anthropology) and Maria Concepcion Sakai (NCIP, Head Office). For assistance with the MPI-EVA sample collection in northern Mindanao, we are especially grateful to Fernando A Almeda Junior, Dr Irinetta C Montinola, Dr Wilfredo Sinco (all from the Surigaonon Heritage Center), Girlie Patagan (NCIP, Surigao), Elizabeth S Larase and .Juliet P Erazo (Office of Non-Formal Education), and the Rotary Club of Surigao. We also thank Peter Ahnert and Holger Kirsten (Department of Biochemistry, University of Leipzig) for support with the MALDI-TOF MS assays and Jody Hey for support with the IM program. We thank the MPI-EVA Molecular Anthropology Group and the Research Group on Comparative Population Linguistics for helpful discussions, in particular Cesare de Filippo and Cristoph Theunert for additional support in computer program implementations.
The authors declare no conflict of interest.
Supplementary Information accompanies the paper on European Journal of Human Genetics website
About this article
Cite this article
Delfin, F., Salvador, J., Calacal, G. et al. The Y-chromosome landscape of the Philippines: extensive heterogeneity and varying genetic affinities of Negrito and non-Negrito groups. Eur J Hum Genet 19, 224–230 (2011). https://doi.org/10.1038/ejhg.2010.162
- genetic affinity
This article is cited by
The Ami and Yami aborigines of Taiwan and their genetic relationship to East Asian and Pacific populations
European Journal of Human Genetics (2021)
The forensic landscape and the population genetic analyses of Hainan Li based on massively parallel sequencing DNA profiling
International Journal of Legal Medicine (2021)
Genetic diversity of the Thao people of Taiwan using Y-chromosome, mitochondrial DNA and HLA gene systems
BMC Evolutionary Biology (2019)
Genetic Architecture of Southeast-coastal Indian tribal populations: A Y-chromosomal phylogenetic analysis
Egyptian Journal of Forensic Sciences (2019)
Scientific Reports (2018)