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Indian Journal of Human Genetics
Medknow Publications on behalf of Indian Society of Human Genetics
ISSN: 0971-6866 EISSN: 1998-362x
Vol. 13, Num. 1, 2007, pp. 16-20

Indian Journal of Human Genetics, Vol. 13, No. 1, January-April, 2007, pp. 16-20

Original Article

Evolution of phenylthiocarbamide taster trait in Mysore, South India

Human Genetics Laboratory, Department of Studies in Zoology, University of Mysore, Manasagangothri, Mysore - 570 006
Correspondence Address:Department of Studies in Zoology, University of Mysore, Manasagangothri, Mysore - 570 006, rnallur@sancharnet.in

Code Number: hg07003

Abstract

Background: The ability to taste phenylthiocarbamide (PTC), a bitter chemical has long been known to be a heritable trait, which is being widely used for both genetic and anthropological studies. The frequency of taster and non-taster allele is found to vary in different populations.
Aims and Objective:
To investigate the frequency of taster trait in Mysore, South India.
Materials and Methods:
The present investigation was conducted in Mysore, South India during 2002 - 2003. About 3282 subjects irrespective of age, sex, religion, food habits, socio-economic status were randomly selected from various parts of the city and a total of 180 families, which included Christian (50), Hindu (61) and Muslim (69) were screened from different localities of the city. Harris and Kalmus method was used to assess the PTC taster and nontaster phenotype.
Results:
It was found that tasters were significantly more frequent than nontasters in all the four categories. The incidence of tasters was more in unbiased category (85%) and less in Muslim category (58%). Investigations on PTC tasting in the families of three different religious groups revealed that the tasters were significantly more frequent than nontasters. It was also found that heterozygous father or mother for the taster genes with nontaster partner had taster and nontaster progenies in the ratio 1.0: 1.54 indicating the deviation in the segregation pattern of test cross.
Conclusion:
In Mysore, tasters are more frequent than nontasters. Variation in the frequency of nontaster allele in the religious groups could be due to inbreeding.

Keywords: Inbreeding, Mysore families, nontaster allele, phenylthiocarbamide taster trait

Introduction

Phenylthiocarbamide (PTC), a bitter chemical synthesized by Fox [1] has been widely used for genetic and anthropological studies. [2] Taste responsiveness to PTC was known to be a heritable trait. The inability to taste PTC is a simple Mendelian recessive trait, [3],[4],[5],[6],[7] wherein the individuals with two recessive alleles (tt) are nontasters for PTC and individuals with one dominant allele (Tt) or two dominant alleles (TT) are tasters for PTC. There are many reports, which contradict this model, some of them are: incomplete dominance, [8] two locus model [9],[10],[11],[12] and polygenic model. [13]

Kim et al[2] have identified a small region on Chromosome 7q by genome-wide linkage analysis, which shows strong linkage disequilibrium between single-nucleotide polymorphism markers and PTC taste sensitivity in unrelated subjects. This region harbors a gene that encodes a member of the TAS2R bitter taste receptor family. A major locus on 7q35-q36 and a secondary locus on Chromosome 16p have also been localized by genome scan for PTC taster gene. [12] Bufe et al[14] have demonstrated that alleles of hTAS2R38 codes for functionally different receptor types that directly affect bitterness perception containing compounds. They suggested that these polymorphisms might be due to evolutionary pressures that foster variability at the receptor to enhance bitter detection and rejection of these compounds. In the present study, we report that the tasters are more frequent than nontasters in Mysore, South India.

Materials and Methods

The present investigation was conducted in Mysore, South India from 2002-2003. About 3282 subjects were randomly selected from various parts of the city irrespective of age, sex, religion, food habits and socio-economic status. Subjects were classified into four different categories viz, unbiased category (= individuals screened randomly in public places without looking into religion, region, age and sex), Hindu, Christian and Muslim religious groups. In order to assess the pattern of inheritance and the frequency of the PTC tasting in different religious groups, a total of 180 families, which included Christian (50), Hindu (61) and Muslim (69) were screened from different localities of the city.

Harris and Kalmus [7] method was used to assess the PTC taster and nontaster phenotype. With their consent, the subjects and their family members were asked to taste the PTC solution and the results were recorded in the proforma used to collect the family history. Information about any possible migration in or out of these families or any associated diseases in the family was also recorded. Pedigrees were constructed based on the information collected from these families. Chi square test was applied to justify the deviations from the expected ratio of taster and nontaster alleles.

One of the limitations of this study was, the number of offspring born in these families were less. However, this can be justified by the fact that in humans each conception is an independent event; the probability of having another child in these families who could be a taster cannot be ruled out. Another limitation is that the availability of families over three to four generations is very rare and even some of these families were not given consent for this study.

Results

PTC taster trait was analyzed in four different categories namely Unbiased, Hindu, Muslim and Christian groups. It was found that tasters were significantly more frequent than nontasters in all the four categories [Table - 1]. The incidence of tasters was more in the unbiased category (85%) and less in the Muslim category (58%). Based on the taster phenotype of the progeny and the parents analyzed in 180 families, five different genotypic groups were classified. They are (a) TT ♂ x TT ♀, (b) Tt ♂ x Tt ♀, (c) TT(t) ♂ x tt ♀, (d) tt ♂ x TT(t) ♀ and (e) tt ♂ x tt ♀. Pedigrees were constructed for all the five different genotypic groups [Figure - 1]. Of the 180 families studied, parents of 55 families were in homozygous dominant for taster trait and parents of 12 families were in heterozygous condition [Table - 2]. Taster parents (67 families) had produced both taster and nontaster children, of which 89% were taster children, whereas nontaster parents (27 families), had produced only nontaster children (100%). [Figure - 2] illustrates the above frequency of distribution of taster gene in 180 families studied.

When one of the parents was a nontaster, the frequency of tasters and nontasters in the progeny varies. By analyzing the taster phenotype of the progeny in the above 86 families, 15 and 12 families had homozygous taster father and mother respectively [Table - 3]. The remaining 59 families, that is, heterozygous father or mother for taster gene with nontaster partners (test cross) had taster and nontaster progenies in the ratio 1.0: 1.54. This indicates the deviation in the segregation pattern with increased variable penetrance of nontaster allele [Figure - 3] in these families.

Discussion

Substantial variation in taste sensitivity exists along with great degree of sequence diversity and variation in bitter taste receptor genes. [2],[15] Wooding et al[16] have examined patterns of DNA sequence variation in the PTC gene of different populations, which accounts for up to 85% of phenotypic variance in the taster trait. They found excess of intermediate-frequency variants than neutral variants and suggested that this variation is due to the balance natural selection, which has acted to maintain "taster" and "nontaster" alleles of the PTC gene. However, the frequency of tasters in different populations as available in the literature indicates that Papago Indians in Arizona shows the highest incidence of tasters (98.6%), while Kondhs population in Orissa, India has shown only 35% of tasters. [12],[17] Studies in other regions showed the frequency of tasters ranged in between the two extreme cases [Table - 4] indicating the wide range of variations found in the frequency of taster and nontaster genotypes. The ability to taste PTC shows complex inheritance in humans. [12] Using quantitative trait locus mapping techniques, Kim et al[2] have found a gene that accounts for 55-85% of the variance in PTC taste sensitivity.

In the present study, the frequency of PTC tasters is greater than nontasters. This is more evident in the unbiased category than the religious groups. However, based on the segregation analysis of heterozygous families, nontaster alleles are increased in their progeny. Since variable penetrance is more common in autosomal dominant condition and deviation in segregation pattern may be due to variable penetrance of taster allele, as heterozygotes cannot be identified. The other possibility that some of the TT x tt marriages may be infact Tt x tt, cannot be ruled out, which may be the reason for deviation in the segregation of taster and nontaster progeny.

Another possibility of the change in the genetic ratio of the PTC taster allele in heterozygotes could be due to inbreeding. The religious groups in India particularly in South India exhibit high level of second degree consanguinity. [18],[19] The inbreeding within these religious groups for several generations and selection of preferentially segregated nontaster allele to the subsequent generations cannot be ruled out. On the other hand, although PTC itself has not been found in nature, the ability to taste PTC is correlated strongly with the ability to taste other naturally occurring bitter substances, many of which are toxic. [20],[21] Therefore, understanding the nature of the variation in bitter taste and its relationship to diet and other behaviors may have important implications on human health.

Acknowledgments

We thank all the individuals and family members who have participated in the present study. We also thank University of Mysore, We thank the Chairmen of our department for the encouragement during the course of this study and our human genetics group for their support and help during the preparation of the manuscript and also Mr. Ivan Aranha for rendering his help during this study[26].

References

1.Fox AL. Tasteblindness. Science 1931;73:14.  Back to cited text no. 1    
2.Kim V, Jorgenson E, Coon H, Leppert M, Risch N, Drayna D. Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide. Science 2003;299:1221-5.  Back to cited text no. 2    
3.Snyder LH. Inherited taste defiency. Science 1931;74:151-2.  Back to cited text no. 3    
4.Blakeslee AF. Genetics of sensory thresholds: Taste for phenylthiocarbamide. Proc Natl Acad Sci 1932;18:120-30.  Back to cited text no. 4  [PUBMED]  [FULLTEXT]
5.Levit SG, Soboleva GV. Comparative intrapair correlations of fraternal twins and siblings. J Hered 1935;30:389-96.   Back to cited text no. 5    
6.Hartmann G. Application of individual taste differences towards Phenylthiocarbamide in genetic investigations. Ann Eugen 1939;9:123-35.  Back to cited text no. 6    
7.Harris H, Kalmus H. The measurement of taste sensitivity to phenylthiourea (PTC). Ann Eugen 1949;15:24-31.  Back to cited text no. 7  [PUBMED]  
8.Reddy BM, Rao DC. Phenylthiocarbamide taste sensitivity revisited: Complete sorting test supports residual family resemblance. Genet Epidemiol 1989;6:413-21.  Back to cited text no. 8  [PUBMED]  
9.Olson JM, Boehnke M, Neiswanger K, Roche AF, Siervogel RM. Alternative genetic models for the inheritance of the phenylthiocarbamide taste deficiency. Genet Epidemiol 1989;6:423-34.   Back to cited text no. 9  [PUBMED]  
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11.Reed DR, Bartoshuk LM, Duffy V, Marino S, Price A. Propylthiouracil tasting: Determination of underlying threshold distributions using maximum likelihood. Chem Sense 1995;20:529-33.   Back to cited text no. 11    
12.Drayna D, Coon H, Kim UK, Elsner T, Cromer K, Otterud B, et al. Genetic analysis of a complex trait in the Utah Genetic reference Project: A major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p. Hum Genet 2003;112:567-72.  Back to cited text no. 12  [PUBMED]  [FULLTEXT]
13.Reed DR, Nanthakumar E, North M, Bell C, Bartoshuk LM, Price RA. Localization of a gene for bitter-taste perception to human chromosome 5p15. Am J Hum Genet 1999;64:1478-80.  Back to cited text no. 13  [PUBMED]  [FULLTEXT]
14.Bufe B, Breslin PA, Kuhn C, Reed DR, Tharp CD, Slack JP, et al. The molecular basis of individual differences in phenylthiocarbamide and propylthiouracil bitterness perception. Curr Biol 2005;15:322-7.  Back to cited text no. 14  [PUBMED]  [FULLTEXT]
15.Tepper BJ. 6-n-Propylthiouracil: A genetic marker for taste, with implications for food preference and dietary habits. Am J Hum Genet 1998;63:1271-6.  Back to cited text no. 15  [PUBMED]  [FULLTEXT]
16.Wooding S, Kim UK, Bamshad MJ, Larsen J, Jorde LB, Drayna D. Natural selection and molecular evolution in PTC, a bitter- taste receptor gene. Am J Hum Genet 2004;74:637-46.  Back to cited text no. 16  [PUBMED]  [FULLTEXT]
17.Guo SW, Shen FM, Wang YD, Zheng CJ. Threshold distributions of phenylthiocarbamide (PTC) in the Chinese populations. Ann NY Acad Sci 1998;855:810-2.  Back to cited text no. 17  [PUBMED]  [FULLTEXT]
18.Bittle AH, Coble JM, Rao NA. Trends in consanguineous marriage in Karnataka, South India, 1980-89. J Biosoc Sci 1993;25:11-6.  Back to cited text no. 18    
19.Krishnamoorthy S, Audinarayana N. Trends in consanguinity in South India. J Biosoc Sci 2001;33:185-97.   Back to cited text no. 19  [PUBMED]  
20.Bergen AW, Caporaso N. Cigarette smoking. J Nat Cancer Inst 1999;91:1365-75.  Back to cited text no. 20  [PUBMED]  [FULLTEXT]
21.Enoch MA, Harris CR, Goldman D. Does a reduced sensitivity to bitter taste increase the risk of becoming nicotine addicted. Addic Behav 2001;26:399-404.  Back to cited text no. 21  [PUBMED]  [FULLTEXT]
22.Saldhana PH, Becak W. Taste threshold for phenylthiocarbamide among Askenazich Jews. Science 1959;129:150-1.  Back to cited text no. 22    
23.Valls AM. As quoted by Sisodia et al. In Genetics and racial aspects of phenylthiocarbamide tasting ability in Indians- International symposium on "The role of Genetics today" September, 1968.  Back to cited text no. 23    
24.Sisodia P, Rao UR. Genetics and racial aspects of phenylthiocarbamide tasting ability in Indians. International symposium on "The role of Genetics today"- September, 1968.   Back to cited text no. 24    
25.Bhatkar RS, Nalluiwar SC, Katti VA. The study of tasters and nontasters of phenylthiocarbamide (PTC) and its relation to blood groups. Indian J Physiol Pharmacol 1989;33:168-70.  Back to cited text no. 25    
26.Guo SW Reed DR. The genetics of phenylthiocarbamide perception. Ann Hum Biol 2001;28:111-42.  Back to cited text no. 26    

Copyright 2007 - Indian Journal of Human Genetics


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