Summary
Karyotypic evaluation of 100 Rajputs and 100 Punjabis revealed different frequencies of Y chromosome polymorphism and minor chromosome variants. Long Y chromosome were observed in 5% of the Rajputs and 3% of the Punjabis. The Y indices of Rajputs were consistently higher than those of Punjabis. Significant differences were noted between Rajputs and Punjabis with respect to the 5 Y indices. Significant differences were also found when these 2 populations were compared with different populations of the world. Minor chromosome variants were observed in 18% of the Rajputs and 19% of the Punjabis.
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Battaglia, E., Guanti, G., Barsanti, P., Petrinelli, P.: Chromosomal survey in 298 normal subjects and 1253 cases of congenital disorders during 1966–1970. Acta Genet. med. (Roma) 20, 123–173 (1971)
Bender, M. A., Gooch, P. C.: An unusually long human Y chromosome. Lancet 1961 II, 463–464
Bishop, A., Blank, C. E., Hunter, H.: Heritable variation in the human Y chromosome. Lancet 1962 II, 18–20
Bobrow, M., Pearson, P. L., Pike, M. C., El-Alfi, O. S.: Length variation in the quinacrine-binding segment of human Y chromosome of different size. Cytogenetics 10, 190–198 (1971)
Bochkov, N. P., Kuleshov, N. P., Chebotarev, A. N., Alekhin, V. I., Midian, S. A.: Population cytogenetic investigation of newborns in Moscow. Humangenetik 22, 139–152 (1974)
Chapelle, A. de la, Aula, P., Kivalo, E.: Enlarged short arm or satellite region — a heritable trait probably unassociated with developmental disorder. Cytogenetics 2, 129–139 (1963a)
Chapelle, A. de la, Hortling, H., Edgrn, J., Kaariainen, R.: Evidence for the existence of heritable large Y chromosomes unassociated with developmental disorders — a cytogenetical and clinical study of four males with hypogonadism, one with mongolism and their relatives. Hereditas (Lund) 50, 351–360 (1963b)
Cohen, M. M., Shaw, M. W., Mac Cluer, J. W.: Racial differences in the length of human Y chromosomes. Cytogenetics 5, 34–52 (1966)
Conen, P. E., Bailey, J. D., Allemang, W. H., Thompson, D. W., Ezrin, C.: A probable partial deletion of the Y chromosome in an intersex patient. Lancet 1961 II, 294–295
Court Brown, W. M.: Human population cytogenetics. Amsterdam: North-Holland 1967
Craig-Holmes, A. P., Moore, F. B., Shaw, M. W.: Polymorphism of human C-band heterochromatin, 1. Frequency of variants. Amer. J. hum. Genet. 25, 181–192 (1973)
Craig-Holmes, A. P., Shaw, M. W.: Polymorphism of human constitutive heterochromatin. Science 174, 702–704 (1971)
Ferguson-Smith, M. A.: Human chromosomes in meiosis. In: Human genetics (eds. Grouchy, Ebling and Henderson), pp. 195–211. Amsterdam: Excerpta Medica 1972
Friedrich, U., Nielsen, J.: Chromosome studies in 5049 consecutive newborn children. Clin. Genet. 4, 333–343 (1973)
Griepenberg, U.: Size variation and orientation of the human Y chromosome. Chromosoma (Berl.) 15, 618–629 (1964)
Hamerton, J. L., Ray, M., Abbot, A., Williamson, C., Ducasse, G. C.: Chromosome studies in a neonatal population. Canad. med. Ass. J. 106, 776–779 (1972)
Huebner, H.: The Y chromosome in selected groups of men of the Polish population. Bull. Acad. pol. Sci.: Ser. Sci. Biol. 19, 467–472 (1971)
Jacobs, P. A., Harden, D. G., cf. Penrose, L. S.: Mongolism. Brit. med. Bull. 17, 184–189 (1961)
Jeske, J., Huebner, H.: A familial variant of the Y chromosome. Endokr. pol. 21, 411–414 (1970)
Kadotani, T., Ohama, K., Takahara, H., Makino, S.: Studies on the Y chromosome in human males from fertile and infertile couples. Jap. J. hum. Genet. 16, 35–41 (1971)
Källen, B., Levan, A.: Abnormal length of chromosomes 21 and 22 in four patients with Marfan's syndrome. Cytogenetics 1, 5–19 (1962)
Kikuchi, Y., Sandberg, A.: Chronology and pattern of human chromosome replication. II. Autoradiographic behaviour of various Y and X chromosomes. J. nat. Cancer Inst. 34, 795–813 (1965)
Klinger, H. P., cf. Fraccaro, M., Lindsten, H.: The nature, origin and genetic implications of structural abnormalities of the sex chromosomes in man. In: Cytogenetics of cells in culture, pp. 27–110. New York: Academic Press 1964
Knuutila, S., Gripenberg, U.: The fluorescence pattern of a human Yq+ chromosome. Hereditas (Lund) 70, 307–308 (1972)
Laberge, C., Gagne, R.: Quinacrine mustard staining solves the length variation of the human Y chromosome. Johns Hopk. Med. J. 128, 79–83 (1971)
Lins, L. E., Sundequist, U.: Y/E index in a Swedish population. Acta Genet. med. (Roma) 20, 211–216 (1971)
Lubs, H. A., Ruddle, F. H.: Chromosomal abnormalities in the human population: estimation of rates based on New Haven new born study. Science 169, 495–497 (1970a)
Lubs, H. A., Ruddle, F. H.: Application of quantitative karyotype to chromosome variation in 4400 consecutive new borns. In: Human population cytogenetics (eds. P. A. Jacobs, W. H. Price, P. Law), pp. 120–142. Edinburgh: University Press 1970b
Lubs, H. A., Ruddle, F. H.: Chromosome polymorphism in American Negro and White populations. Nature (Lond.) 233, 134–136 (1971)
Makino, S., Muramoto, J.: Some observations on the variability of the Y chromosome. Proc. Jap. Acad. 40, 757–761 (1965)
Makino, S., Sasaki, M. S., Yamada, K., Kajii, T.: A long Y chromosome in man. Chromosoma (Berl.) 14, 154–161 (1963)
Makino, S., Takagi, N.: Some morphological aspects of the abnormal human Y chromosome. Cytologia (Tokyo) 30, 273–292 (1965)
Mc Kenzie, W. H., Hostelter, T. L., Lubs, H. A.: Y family study: heritable variation in the length of the human Y chromosome. Amer. J. hum. Genet. 24, 686–693 (1972)
Meisner, L. L., Inhorn, S. L.: Normal male development with Y chromosome long arm deletion (Yq-). J. med. Genet. 9, 373–377 (1972)
Mikelsaar, A.-V. N., Tuur, S. J., Kaosaar, M. E.: Human karyotype polymorphism. I. Routine and fluorescence microscopic investigation of chromosomes in a normal adult population. Humangenetik 20, 89–102 (1973)
Moorhead, P. S., Nowell, P. C., Mellman, W. J., Battips, D. M., Hungerford, D. A.: Chromosome preparations of leukocytes cultured from human peripheral blood. Exp. Cell Res. 20, 613–616 (1960)
Muldal, S., Ockey, C. H.: Muscular dystrophy and deletions of Y chromosomes. Lancet 1961 II, 601
Nakagome, Y., Sasaki, M., Matusi, I., Kawazura, M., Fakuyama, Y.: A mentally retarded boy with a minute chromosome. J. Pediat. 67, 1163–1167 (1965)
Nielsen, J.: Large Y and enlarged short arms of a small acrocentric chromosome. Hereditas (Lund) 61, 416–421 (1969)
Nielsen, J., Friedrich, U.: Length of the Y chromosome in criminal males. Clin. Genet. 3, 281–285 (1972)
Nielsen, J., Henriksen, R.: Incidence of chromosome aberrations among males in a Danish youth prison. Acta psychiat. scand. 48, 87–102 (1972)
Nuzzo, F., Bompiani, A., Moneta, E., Caviezel, F., Mussinelli, P.: Observations on some of structural variations in the Y chromosome in man. Atti Ass. Genet. Ital. 12, 191–201 (1967)
Nuzzo, F., Caviegel, F., Carli, L.de.: Y chromosome and exclusion of paternity. Lancet 1966 I, 260–262
Robinson, J. A., Buckton, K. A.: Quinacrine fluorescence of variant and abnormal human Y chromosomes. Chromosoma (Berl.) 35, 342–352 (1971)
Sands, V. E.: Short arm enlargement of acrocentric chromosomes. Amer. J. hum. Genet. 21, 293–304 (1969)
Schnedl, W.: Analysis of the length variation in the human Y chromosome by aids of the quinacrine fluorochrome method. Humangenetik 12, 188–194 (1971)
Soudek, D., Longmuir, V., Stewart, D. J.: Variation in the nonfluorescent segment of long Y chromosome. Humangenetik 18, 285–290 (1973)
Stern, C., Centerwall, W. R., Sarkar, S. S.: New data on the problem of Y-linkage of hairy pinnae. Amer. J. hum. Genet. 16, 455–471 (1974)
Sugahara, T., Sakurai, M.: Chromosome studies in a family with an abnormally large Y chromosome. Jap. J. hum. Genet. 12, 190–196 (1967)
Surana, R. B., Forbath, P., Conen, P. E.: Minute Y chromosome. Ann. Génét. 14, 145–148 (1971)
Tishler, P. V., Lamborot-Manzur, M., Atteins, L.: Polymorphisms of the human Y chromosome; Fluorescence microscopic studies on the sites of morphologic variation. Clin. Genet. 3, 116 (1972)
Tonomura, A., Ono, H.: Variation in length of the Y chromosome in man. Jap. Nat. Inst. Gen. Report 14, 131 (1963)
Torre, C. de la, Gimenez-Martin, G.: The hyman Y chromosome in the Spanish population. J. Génét. hum. 18, 235–264 (1970)
Unnerus, V., Fellman, J., Chapelle, A. de la: The length of the human Y chromosome. Cytogenetics 6, 213–227 (1967)
Vaharu, T., Patton, R. G., Voorhess, M. L., Gardner, L. I.: Gonadal dysgenesis and enlarged phallus in a girl with 45 chromosomes plus fragment. Lancet 1961 I, 218
Van Wijck, J. A. M., Tijdink, G. A. J., Stette, L. A. M.: Anomalies in the Y chromosome. Lancet 1962 I, 218
Wahlström, J.: Are variations in length of Y chromosome due to structural changes. Hereditas (Lund) 69, 125–128 (1971)
Walzer, S., Breau, G., Gerald, P. S.: A chromosome survey of 2,400 normal newborn infants. J. Pediat. 74, 438–448 (1969)
Wennstörm, J., Chapelle, A. de la: Elongation as the possible mechanism of the origin of large human Y chromosomes. Hereditas (Lund) 50, 345–350 (1963)
Zankl, H., Zang, K. D.: Structural variability of the normal human karyotype. Humangenetik 13, 160–162 (1971)
Zeuthen, E., Nielsen, J.: Length of the Y chromosome in a general male population. Acta Genet. med. (Roma) 22, 45–49 (1973)
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This work was aided by CSIR Grant No. 7/45(458)/71-GAU.I.
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Ghosh, P.K., Singh, I.P. Morphological variability of the human chromosomes in two Indian populations — Rajputs and Punjabis. Hum Genet 29, 67–78 (1975). https://doi.org/10.1007/BF00273352
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DOI: https://doi.org/10.1007/BF00273352