Fixation index

Fixation index (FST) is a measure of population differentiation due to genetic structure. It is frequently estimated from genetic polymorphism data, such as single-nucleotide polymorphisms (SNP) or microsatellites. Developed as a special case of Wright's F-statistics, it is one of the most commonly used statistics in population genetics.

Definition

Two of the most commonly used definitions for FST at a given locus are based on the variance of allele frequencies between populations, and on the probability of Identity by descent.

If is the average frequency of an allele in the total population, is the variance in the frequency of the allele between different subpopulations, weighted by the sizes of the subpopulations, and is the variance of the allelic state in the total population, FST is defined as [1]

Wright's definition illustrates that FST measures the amount of genetic variance that can be explained by population structure. This can also be thought of as the fraction of total diversity that is not a consequence of the average diversity within subpopulations, where diversity is measured by the probability that two randomly selected alleles are different, namely . If the allele frequency in the th population is and the relative size of the th population is , then

Alternatively,[2]

where is the probability of identity by descent of two individuals given that the two individuals are in the same subpopulation, and is the probability that two individuals from the total population are identical by descent. Using this definition, FST can be interpreted as measuring how much closer two individuals from the same subpopulation are, compared to the total population. If the mutation rate is small, this interpretation can be made more explicit by linking the probability of identity by descent to coalescent times: Let T0 and T denote the average time to coalescence for individuals from the same subpopulation and the total population, respectively. Then,

This formulation has the advantage that the expected time to coalescence can easily be estimated from genetic data, which led to the development of various estimators for FST.

Estimation

In practice, none of the quantities used for the definitions can be easily measured. As a consequence, various estimators have been proposed. A particularly simple estimator applicable to DNA sequence data is:[3]

where and represent the average number of pairwise differences between two individuals sampled from different sub-populations () or from the same sub-population (). The average pairwise difference within a population can be calculated as the sum of the pairwise differences divided by the number of pairs. However, this estimator is biased when sample sizes are small or if they vary between populations. Therefore, more elaborate methods are used to compute FST in practice. Two of the most widely used procedures are the estimator by Weir & Cockerham (1984),[4] or performing an Analysis of molecular variance. A list of implementations is available at the end of this article.

Interpretation

This comparison of genetic variability within and between populations is frequently used in applied population genetics. The values range from 0 to 1. A zero value implies complete panmixis; that is, that the two populations are interbreeding freely. A value of one implies that all genetic variation is explained by the population structure, and that the two populations do not share any genetic diversity.

For idealized models such as Wright's finite island model, FST can be used to estimate migration rates. Under that model, the migration rate is

.

The interpretation of FST can be difficult when the data analyzed are highly polymorphic. In this case, the probability of identity by descent is very low and FST can have an arbitrarily low upper bound, which might lead to misinterpretation of the data. Also, strictly speaking FST is not a genetic distance, as it does not satisfy the triangle inequality. As a consequence new tools for measuring genetic differentiation continue being developed.

FST in humans

Autosomal genetic distances based on classical markers

In their study The History and Geography of Human Genes (1994), Cavalli-Sforza, Menozzi and Piazza provide some of the most detailed and comprehensive estimates of genetic distances between human populations, within and across continents. Their initial database contains 76,676 gene frequencies (using 120 blood polymorphisms), corresponding to 6,633 samples in different locations. By culling and pooling such samples, they restrict their analysis to 491 populations. They focus on aboriginal populations that were at their present location at the end of the 15th century when the great European migrations began.[5] When studying genetic difference at the world level, the number is reduced to 42 representative populations, aggregating subpopulations characterized by a high level of genetic similarity. For these 42 populations, Cavalli-Sforza and coauthors report bilateral distances computed from 120 alleles. alleles. Among this set of 42 world populations, the greatest genetic distance observed is between Mbuti Pygmies and Papua New Guineans, where the Fst distance is 0.4573, while the smallest genetic distance (0.0021) is between the Danish and the English. When considering more disaggregated data for 26 European populations, the smallest genetic distance (0.0009) is between the Dutch and the Danes, and the largest (0.0667) is between the Lapps and the Sardinians. The mean genetic distance among the 861 available pairs in the world population is 0.1338. Here are some Fst calculated by Cavalli-Sforza 1994 for some populations :

Fst (Cavalli 1994) W.African Berber Indian Iranian Near Eastern Japanese Basque Lapp Sardinian Danish English Greek Italian
W.African0164217481796145422521299168920621459148713561794
Berber164204974082631707392736619313273429315
Indian17484970154229718418459449293280272261
Iranian17964081540158105928542331417919770133
Near Eastern145426322915801056246423329238236129208
Japanese22521707718105910560148194715581176124411751145
Basque129939241828524614810629348184119231141
Lapp16897364594234239476290667334404308339
Sardinian206261944931432915583486670348340190221
Danish1459313293179238117618433434802119172
English1487273280197236124411940434021020451
Greek1356429272701291175231308190191204077
Italian179431526113320811451413392217251770

Autosomal genetic distances based on SNPs

More recently, the International HapMap Project estimated FST for three human populations using SNP data. Across the autosomes, FST was estimated to be 0.12. The significance of this FST value in humans is contentious. As an FST of zero indicates no divergence between populations, whereas an FST of one indicates complete isolation of populations, Anthropologists often cite Lewontin's 1972 work which came to a similar value and interpreted this number as meaning there was little biological differences between human races.[6] On the other hand, while an FST value of 0.12 is lower than that found between populations of many other species, Henry Harpending argued that this value implies on a world scale a "kinship between two individuals of the same human population is equivalent to kinship between grandparent and grandchild or between half siblings".[7]

Intercontinental autosomal genetic distances based on SNPs[8]
Europe (CEU) Sub-Saharan Africa (Yoruba) East-Asia (Japanese)
Sub-Saharan Africa (Yoruba) 0.153
East-Asia (Japanese) 0.111 0.190
East-Asia (Chinese) 0.110 0.192 0.007
Intra-European/mediterranean autosomal genetic distances based on SNPs[8][9]
Italians Palestinians Swedish Finns Spanish Germans Russians French Greeks
Palestinians 0.0064
Swedish 0.0064-0.0090 0.0191
Finns 0.0130-0.0230 0.0050-0.0110
Spanish 0.0010-0.0050 0.0101 0.0040-0055 0.0110-0.0170
Germans 0.0029-0.0080 0.0136 0.0007-0.0010 0.0060-0.0130 0.0015-0.0030
Russians 0.0088-0.0120 0.0202 0.0030-0.0036 0.0060-0.0120 0.0070-0.0079 0.0030-0.0037
French 0.0030-0.0050 0.0020 0.0080-0.0150 0.0010 0.0010 0.0050
Greeks 0.0000 0.0057 0.0084 0.0035 0.0039 0.0108

Programs for calculating FST

Modules for calculating FST

References

  1. Holsinger, Kent E.; Bruce S. Weir (2009). "Genetics in geographically structured populations: defining, estimating and interpreting FST". Nat Rev Genet. 10 (9): 639–650. doi:10.1038/nrg2611. ISSN 1471-0056. PMID 19687804.
  2. Richard Durrett (12 August 2008). Probability Models for DNA Sequence Evolution. Springer. ISBN 978-0-387-78168-6. Retrieved 25 October 2012.
  3. Hudson, RR.; Slatkin, M.; Maddison, WP. (Oct 1992). "Estimation of Levels of Gene Flow from DNA Sequence Data". Genetics. 132 (2): 583–9. PMC 1205159Freely accessible. PMID 1427045.
  4. Weir, B. S.; Cockerham, C. Clark (1984). "Estimating F-Statistics for the Analysis of Population Structure". Evolution. 38 (6): 1358. doi:10.2307/2408641. ISSN 0014-3820.
  5. Cavalli-Sforza et al., 1994, p. 24
  6. Lewontin, Richard C. (1972). "The apportionment of human diversity". Evolutionary biology. 6 (38): 381–398. doi:10.1007/978-1-4684-9063-3_14.
  7. Harpending, Henry (2002-11-01). "Kinship and Population Subdivision" (PDF). Population & Environment. 24 (2): 141–147. doi:10.1023/A:1020815420693. JSTOR 27503827.
  8. 1 2 Nelis, Mari; et al. (2009-05-08). Fleischer, Robert C., ed. "Genetic Structure of Europeans: A View from the North–East". PLoS ONE. 4 (5): e5472. Bibcode:2009PLoSO...4.5472N. doi:10.1371/journal.pone.0005472. PMC 2675054Freely accessible. PMID 19424496., see table
  9. Tian, Chao; et al. (November 2009). "European Population Genetic Substructure: Further Definition of Ancestry Informative Markers for Distinguishing among Diverse European Ethnic Groups". Molecular Medicine. 15 (11-12): 371–383. doi:10.2119/molmed.2009.00094. ISSN 1076-1551. PMC 2730349Freely accessible. PMID 19707526., see table
  10. Crawford, Nicholas G. (2010). "smogd: software for the measurement of genetic diversity". Molecular Ecology Resources. 10 (3): 556–557. doi:10.1111/j.1755-0998.2009.02801.x. PMID 21565057.

Further reading

  • Evolution and the Genetics of Populations Volume 2: the Theory of Gene Frequencies, pg 294–295, S. Wright, Univ. of Chicago Press, Chicago, 1969
  • A haplotype map of the human genome, The International HapMap Consortium, Nature 2005

External links

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