Princess Ngonnso ´ and the foundation of the royal house of Nso ´

1
Princess Ngonnso´ and the foundation of the royal house of Nso´ Before the arrival of European colonists in the nineteenth century the Nso´ royal family, headed by the ‘Fon’, ruled an empire of some 2600km 2 in the western Grassfields of Cameroon with the royal palace located in Kumbo. The Nso´ comprise over 200,000 citizens divided groups (CLGs) (table 1). It is thought that previously common NRY lineages may have been replaced by a lineage associated with the expansion of the Bantu-speaking peoples, namely E3a 7 . We have found evidence that suggests haplogroup Y*(xBR,A3b2) is one of these replaced lineages. It is found at very low frequencies (<14%) in populations distributed throughout sub-Saharan Africa and the STR haplotype distribution displays a high among group variance (assessed using AMOVA 8 ) of 85.64%, which is consistent with inter-group isolation. This is in contrast to the modal haplogroup E3a with an among group variance of only 3.05%, a low figure which is consistent with high inter-group geneflow or a recent common origin. We suggest that Y*(xBR,A3b2) may have been predominant in pre-Bantu-speaking hunter- Our aim was to examine which of the different variations of the oral history describing the foundation of the Nso´, if any, was best supported by sex-specific genetic data, where each account would generate separate expectations for the distribution of the non-recombining portion of the Y- chromosome (NRY) and mitochondrial DNA (mtDNA) types. Given certain social characteristics of the Nso´, such as the strict rules governing membership to the Wonto´ and the high level of polygamy, NRY types found in the Wonto´ would be expected to be more homogenous than the other CLGs while there would be no difference in the distribution of mtDNA types. Additionally, if all Nso´ Fons are direct paternal descendants of a Visale chief and Y*(xBR,A3b2) was characteristic of the hunter-gatherer Visale (see Box 1) then this would be expected to be the modal NRY haplogroup amongst the Wonto´ and this NRY type with respect to a battery of STRs. We typed the NRY 2 of 151 samples from Kumbo and 1087 samples from 12 other Grassfield towns (Figure 1), including seven in the Tikar region, for 12 Unique Event Polymorphisms (UEPs) and six Short Tandem Repeats (STRs) (for the definition of NRY haplogroups and high resolution haplotypes respectively) and grouped them according to self declared cultural identity (including Nso´ CLG where applicable). Additionally, the mtDNA HVS-1 region and specific coding region The modal haplogroup of the Wonto´ was Y*((xBR,A3b2), with a frequency of 56%, and all members of this haplogroup had identical STR haplotypes (coined the Nso´ Royal modal haplotype (NRMH)). In contrast the modal haplogroup in the other CLGs was E3a (see table 2) with a diverse range of STR haplotypes (gene diversity = 0.9438 ± 0.0114 4 ). A known paternal descendant of a recent Fon also possessed the NRMH. Table 2: NRY UEP haplogroup numbers found in the four Nso´ CLGs. Corresponding relative frequencies are shown in brackets. Haplogroup nomenclature is that proposed by the Y Chromosome Consortium 3 . Only 1 out of 780 self declared non-Nso ´ from the Grassfields had a Y*(xBR,A3b2) chromosome and this individual was born in Kumbo, the Nso´ capital. Thus there was significant population differentiation between the Wonto´ and all other populations (Figure 2). Pairwise comparisons of the four Nso´ CLGs showed no statistical difference in the frequency of mtDNA types (Fisher’s exact P values 5 > 0.28549). We estimated a time to the most recent common ancestor 6 for the Y*(xBR,A3b2) NRY type found in the Nso´ of 519-601 years (95% CI: 67-2,420), a date which correlated well with the oral history The data generated was in concordance with the most common origin story of a Princess migrating and marrying a local Visale, rather than being accompanied by a Tikar husband. We have demonstrated that genetic analysis can be a useful tool joining other disciplines such as anthropology and linguistics in investigations of the histories of groups living in sub- Saharan Africa, especially those for whom prehistory is recent and where archaeological evidence is sparse. Box 1-The replacement of hunter gatherers by Bantu- speaking farmers We thank all sample donors, the BBSRC, Dallas Swallow and Abigail Jones as well as Richard Phillips and Ali Barwani who performed some of the typing. CLG Membership Criteria Wonto´ Descendants of a Fon up to the fourth generation (for men) and third generation (for women) - the Royal family Duy Descendants of a Fon who ruled more than four generations ago (for men) and three generations ago (for women) Nshiyla v Subjects born into Palace servitude Mtaar Commoners Nso´ CLG Assigned NRY Haplogroup P*(xR1a ) BR*(xDE,JR ) E*(xE3a ) Y*(xBR,A3b2 ) E3a Wonto´ (n=18) 0 (0.000) 2 (0.111) 0 (0.000) 10 (0.556) 6 (0.333) Duy (n=51) 1 (0.020) 0 (0.000) 2 (0.039) 9 (0.176) 39 (0.765) Nshiyla v (n=42) 0 (0.000) 1 (0.024) 1 (0.024) 8 (0.190) 32 (0.762) Mtaar (n=21) 0 (0.000) 0 (0.000) 0 (0.000) 3 (0.143) 18 (0.857) Total (n=132) 1 (0.008) 3 (0.023) 3 (0.023) 30 (0.227) 95 (0.720) Figure 1: A map showing the area of Cameroon studied and the specific towns DNA was collected from. Table 1: The four Nso´ social CLGs and the criteria for membership to the corresponding CLG. Figure 2: A principle co-ordinate plot (PCO) of population pairwise Fst genetic distances calculated using NRY UEP haplogroup frequencies of the four Nso´ CLGs (labelled by name) and other Grassfield populations (labelled corresponding to the key adjacent to the plot). PCO1 and PCO2 explain 76.94% and 13.65% of the variation respectively. The Nso´ have a detailed oral history of their origins, which dates to 250- 700 years before present. The most common account tells of a Princess Ngonnso´ travelling from the Tikar Kingdom, approximately 100 km to the east, and encountering a small indigenous group of hunter gatherers (the Visale) by whom she was warmly welcomed. Her son was consequently made the first Fon of the Nso´ and it is from him that the current Fon is said to be directly descended along the paternal line. However, opinion differs as to whether the Princess came with a husband from Tikar 1 or married a local Visale chief. Introduction Objectives Hypothesis Results Conclusion Acknowledgments 1. Mzeka,N.P. The Core Culture of Nso'. Jerome Radin Co., Agawam, Ma. (1978). 2. Thomas,M.G., Bradman,N. & Flinn,H.M. High throughput analysis of 10 microsatellite and 11 diallelic polymorphisms on the human Y- chromosome. Hum. Genet. 105, 577-581 (1999). 3. The Y Chromosome Consortium. A Nomenclature System for the Tree of Human Y-Chromosomal Binary Haplogroups. Genome Res. 12, 339-348 (2002). 4. Nei,M. Molecular Evolutionary Genetics. Columbia University Press, (1987). 5. Raymond,M. & Rousset,F. An Exact Test for Population Differentiation. Evolution 49, 1280-1283 (1995). 6. Behar,D.M. et al. Multiple origins of Ashkenazi Levites: Y chromosome evidence for both Near Eastern and European ancestries. Am. J. Hum. Genet. 73, 768-779 (2003). 7. Underhill,P.A. et al. The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations. Ann. Hum. Genet. 65, 43-62 (2001). 8. Excoffier,L., Smouse,P.E. & Quattro,J.M. Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics 131, 479-491 (1992). References Method The Centre for Genetic Anthropology, Department of Biology, University College London K. R. Veeramah, D. Zeitlyn, V. G. Fanso, B. A. Connell, M. E. Weale, N. Bradman and M. G. Thomas. Genetics in support of Oral History Interpolated contour map of square root of E3a haplogroup frequencies in populations in sub-Saharan Africa. Position of populations actually collected are indicated by . Interpolated contour map of square root of Y*(xBR,A3b2) haplogroup frequencies in populations in sub- Saharan Africa. The square root transformation was used to aid in the visualisation of low Y*(xBR,A3b2) frequencies. D uy M taar W onto' Nshiylav -0.3 -0.2 -0.1 0 0.1 0.2 0.3 -0.4 -0.2 0 0.2 0.4 0.6 0.8 1 PCO1 PCO2 A ghem Bafut Bafut-Tikar Bam un Kwandja Bamileke M ambila Tikar Yam ba W imbum

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Princess Ngonnso ´ and the foundation of the royal house of Nso ´. Genetics in support of Oral History. K. R. Veeramah, D. Zeitlyn, V. G. Fanso, B. A. Connell, M. E. Weale, N. Bradman and M. G. Thomas. The Centre for Genetic Anthropology, Department of Biology, University College London. - PowerPoint PPT Presentation

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Princess Ngonnso´ and the foundation of the royal house of Nso´

Before the arrival of European colonists in the nineteenth century the Nso´ royal family, headed by the ‘Fon’, ruled an empire of some 2600km2 in the western Grassfields of Cameroon with the royal palace located in Kumbo. The Nso´ comprise over 200,000 citizens divided into four caste-like groups (CLGs) (table 1).

It is thought that previously common NRY lineages may have been replaced by a lineage associated with the expansion of the Bantu-speaking peoples, namely E3a7. We have found evidence that suggests haplogroup Y*(xBR,A3b2) is one of these replaced lineages. It is found at very low frequencies (<14%) in populations distributed throughout sub-Saharan Africa and the STR haplotype distribution displays a high among group variance (assessed using AMOVA8) of 85.64%, which is consistent with inter-group isolation. This is in contrast to the modal haplogroup E3a with an among group variance of only 3.05%, a low figure which is consistent with high inter-group geneflow or a recent common origin. We suggest that Y*(xBR,A3b2) may have been predominant in pre-Bantu-speaking hunter-gatherers.

Our aim was to examine which of the different variations of the oral history describing the foundation of the Nso´, if any, was best supported by sex-specific genetic data, where each account would generate separate expectations for the distribution of the non-recombining portion of the Y-chromosome (NRY) and mitochondrial DNA (mtDNA) types.

Given certain social characteristics of the Nso´, such as the strict rules governing membership to the Wonto´ and the high level of  polygamy, NRY types found in the Wonto´ would be expected to be more homogenous than the other CLGs while there would be no difference in the distribution of mtDNA types. 

Additionally, if all Nso´ Fons are direct paternal descendants of a Visale chief and Y*(xBR,A3b2) was characteristic of the hunter-gatherer Visale (see Box 1) then this would be expected to be the modal NRY haplogroup amongst the Wonto´ and this NRY type would be relatively homogenous with respect to a battery of STRs.

We typed the NRY2 of 151 samples from Kumbo and 1087 samples from 12 other Grassfield towns (Figure 1), including seven in the Tikar region, for 12 Unique Event Polymorphisms (UEPs) and six Short Tandem Repeats (STRs) (for the definition of NRY haplogroups and high resolution haplotypes respectively) and grouped them according to self declared cultural identity (including Nso´ CLG where applicable). Additionally, the mtDNA HVS-1 region and specific coding region markers were typed in Nso´ samples for assignment to predefined mtDNA haplogroups.

The modal haplogroup of the Wonto´ was Y*((xBR,A3b2), with a frequency of 56%, and all members of this haplogroup had identical STR haplotypes (coined the Nso´ Royal modal haplotype (NRMH)). In contrast the modal haplogroup in the other CLGs was E3a (see table 2) with a diverse range of STR haplotypes (gene diversity = 0.9438 ± 0.01144). A known paternal descendant of a recent Fon also possessed the NRMH.

Table 2: NRY UEP haplogroup numbers found in the four Nso´ CLGs. Corresponding relative frequencies are shown in brackets. Haplogroup nomenclature is that proposed by the Y Chromosome Consortium3.

Only 1 out of 780 self declared non-Nso´ from the Grassfields had a Y*(xBR,A3b2) chromosome and this individual was born in Kumbo, the Nso´ capital. Thus there was significant population differentiation between the Wonto´ and all other populations (Figure 2).

Pairwise comparisons of the four Nso´ CLGs showed no statistical difference in the frequency of mtDNA types (Fisher’s exact P values5 > 0.28549).

We estimated a time to the most recent common ancestor6 for the Y*(xBR,A3b2) NRY type found in the Nso´ of 519-601 years (95% CI: 67-2,420), a date which correlated well with the oral history of when the first Fon of Nso´ ruled.

The data generated was in concordance with the most common origin story of a Princess migrating and marrying a local Visale, rather than being accompanied by a Tikar husband.

We have demonstrated that genetic analysis can be a useful tool joining other disciplines such as anthropology and linguistics in investigations of the histories of groups living in sub-Saharan Africa, especially those for whom prehistory is recent and where archaeological evidence is sparse.

Box 1-The replacement of hunter gatherers by Bantu-speaking farmers

We thank all sample donors, the BBSRC, Dallas Swallow and Abigail Jones as well as Richard Phillips and Ali Barwani who performed some of the typing.

CLG Membership Criteria

Wonto´Descendants of a Fon up to the fourth generation (for men) and third generation (for women) - the Royal family

DuyDescendants of a Fon who ruled more than four generations ago (for men) and three generations ago (for women)

Nshiylav Subjects born into Palace servitude

Mtaar Commoners

Nso´ CLG

Assigned NRY Haplogroup

P*(xR1a) BR*(xDE,JR) E*(xE3a) Y*(xBR,A3b2) E3a

Wonto´

(n=18) 0

(0.000)

2(0.111)

0(0.000)

10(0.556)

6(0.333)

Duy

(n=51) 1

(0.020)

0(0.000)

2(0.039)

9(0.176)

39(0.765)

Nshiylav (n=42)

0(0.000)

1(0.024)

1(0.024)

8(0.190)

32(0.762)

Mtaar

(n=21)0

(0.000)

0(0.000)

0(0.000)

3(0.143)

18(0.857)

Total

(n=132) 1

(0.008)

3(0.023)

3(0.023)

30(0.227)

95

(0.720)

Figure 1: A map showing the area of Cameroon studied and the specific towns DNA was collected from.

Table 1: The four Nso´ social CLGs and the criteria for membership to the corresponding CLG.

Figure 2: A principle co-ordinate plot (PCO) of population pairwise Fst genetic distances calculated using NRY UEP haplogroup frequencies of the four Nso´ CLGs (labelled by name) and other Grassfield populations (labelled corresponding to the key adjacent to the plot). PCO1 and PCO2 explain 76.94% and 13.65% of the variation respectively.

The Nso´ have a detailed oral history of their origins, which dates to 250-700 years before present. The most common account tells of a Princess Ngonnso´ travelling from the Tikar Kingdom, approximately 100 km to the east, and encountering a small indigenous group of hunter gatherers (the Visale) by whom she was warmly welcomed. Her son was consequently made the first Fon of the Nso´ and it is from him that the current Fon is said to be directly descended along the paternal line. However, opinion differs as to whether the Princess came with a husband from Tikar1 or married a local Visale chief.

Introduction

Objectives

Hypothesis

Results

Conclusion

Acknowledgments

1. Mzeka,N.P. The Core Culture of Nso'. Jerome Radin Co., Agawam, Ma. (1978). 2. Thomas,M.G., Bradman,N. & Flinn,H.M. High throughput analysis of 10 microsatellite and 11

diallelic polymorphisms on the human Y-chromosome. Hum. Genet. 105, 577-581 (1999).3. The Y Chromosome Consortium. A Nomenclature System for the Tree of Human Y-

Chromosomal Binary Haplogroups. Genome Res. 12, 339-348 (2002).4. Nei,M. Molecular Evolutionary Genetics. Columbia University Press, (1987).5. Raymond,M. & Rousset,F. An Exact Test for Population Differentiation. Evolution 49, 1280-

1283 (1995).6. Behar,D.M. et al. Multiple origins of Ashkenazi Levites: Y chromosome evidence for both Near

Eastern and European ancestries. Am. J. Hum. Genet. 73, 768-779 (2003).7. Underhill,P.A. et al. The phylogeography of Y chromosome binary haplotypes and the origins of

modern human populations. Ann. Hum. Genet. 65, 43-62 (2001).8. Excoffier,L., Smouse,P.E. & Quattro,J.M. Analysis of molecular variance inferred from metric

distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics 131, 479-491 (1992).

References

Method

The Centre for Genetic Anthropology, Department of Biology, University College London

K. R. Veeramah, D. Zeitlyn, V. G. Fanso, B. A. Connell, M. E. Weale, N. Bradman and M. G. Thomas.

Genetics in support of Oral History

Interpolated contour map of square root of E3a haplogroup frequencies in populations in sub-Saharan Africa. Position of populations actually collected are indicated by .

Interpolated contour map of square root of Y*(xBR,A3b2) haplogroup frequencies in populations in sub-Saharan Africa. The square root transformation was used to aid in the visualisation of low Y*(xBR,A3b2) frequencies.

Duy

Mtaar

Wonto'

Nshiylav

-0.3

-0.2

-0.1

0

0.1

0.2

0.3

-0.4 -0.2 0 0.2 0.4 0.6 0.8 1PCO1

PC

O2

Aghem

Bafut

Baf ut-Tikar

Bamun

Kwandja

Bamileke

Mambila

Tikar

Yamba

Wimbum