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Ribosomal RNA, Maternal Age, and Down's Syndrome*

Published online by Cambridge University Press:  01 August 2014

F. Salamanca-Gomez*
Affiliation:
National Institute for Special Programs of Health, INPES, Bogotà, Colombia
*
Department of Genetics, Pediatric Hospital, National Medical Centre, Instituto Mexicano del Seguro Social, Apartado Postal 12-951, México 12, D.F., México

Abstract

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A selective loss (or a blocking) of rRNA genes in ageing oocytes, and its compensation through the retention of an acrocentric nucleolar organizer chromosome, is proposed as a possible mechanism responsible for the increased frequency of Down's syndrome with maternal age.

Riassunto

RIASSUNTO

Viene proposta, quale meccanismo per cui la frequenza della sindrome di Down aumenta con l'età materna, una perdita selettiva di geni di rRNA, oppure il loro blocco in oociti, compensata dal trattenimento di un cromosoma organizzatore nucleolare acrocentrico.

Résumé

RÉSUMÉ

L'on propose, comme mécanisme par lequel la fréquence du syndrome de Down augmente avec l'âge maternel, une perte sélective de gènes de rRNA, ou bien leur blocage dans les oocytes, compensée par l'entretien d'un chromosome organisateur nucléolaire acrocentrique.

Zusammenfassung

ZUSAMMENFASSUNG

Es wird angenommen, dass das vermehrte Auftreten des Downschen Syndroms bei zunehmendem Alter der Mütter darauf beruht, dass die rRNA-Gene entweder einen selektiven Verlust erleiden oder in Oozyten blockiert werden, wobei zum Ausgleich eines akrozentrischen Nukleolus-Organisator Chromosom festgehalten wird.

Type
Research Article
Copyright
Copyright © The International Society for Twin Studies 1975

Footnotes

*

Partially supported by a grant from the Ford Foundation.

References

REFERENCES

Arrighi, F.E., Hsu, T.C. 1971. Localization of heterochromatin in human chromosomes. Cytogenetics, 10: 8186.Google Scholar
Barath, F., Kuntzel, J. 1972. Induction of mitochondrial RNA polymerase in Neurospora crassa. Nature [New Biol.], 240: 195197.Google Scholar
Berry, R.O. 1941. Chromosome behavior in the germ cells and development of the gonads in Sciara ocellaris. J. Morphol., 68: 547552.Google Scholar
Bodmer, W.F. 1961. Effects of maternal age on the incidence of congenital abnormalities in mouse and man. Nature, 190: 11341135.Google Scholar
Brachet, J. 1943. La localization des acides pentosenucleiques dans les tissues animaux et les oeufs d'amphibiens en voie de dévélopment. Arch. Biol., 53: 207217.Google Scholar
Brown, D.D., Littna, E. 1964. RNA synthesis during the development of Xenopus laevis, the South African claxed toad. J. Mol. Biol., 8: 669674.Google Scholar
Brown, D.D., David, B. 1968. Specific gene amplification in oocytes. Science, 160: 272273.Google Scholar
Brown, D.D., Weber, C.S. 1968. Gene linkage by RNA-DNA hybridization. I. Unique DNA sequences homologous to 4S RNA, 5S RNA and ribosomal RNA. J. Mol. Biol., 32: 661668.Google Scholar
Davidson, E.H. 1968. Gene Activity in Early Development. New York and London: Academic Press.Google Scholar
Dutrilleaux, B., Lejeune, J. 1970. Etude de la déscendance des individus porteurs d'une translocation t(Dq Dq). Ann. Genet., 13: 1119.Google Scholar
Edstrom, J.E., Gall, J.G. 1963. The base composition of ribonucleic acid in lampbrush chromosomes, nucleoli, nuclear sap, and cytoplasma of Triturus oocytes. J. Cell. Biol., 19: 279281.Google Scholar
Elsdale, T.R., Fischberg, M., Smith, S. 1958. A mutation that reduces nucleolar number in Xenopus laevis. Exptl. Cell. Res., 14: 642644.Google Scholar
Ferguson-Smith, M.A., Handmaker, S.D. 1961. Observations on the satellited human chromosomes. Lancet, 1: 638640.Google Scholar
Ferguson-Smith, M.A. 1964. The sites of nucleolus formation in human pachytene chromosomes. Cytogenetics, 3: 124134.Google Scholar
Fialkow, P.J. 1964. Autoimmunity: a predisposing factor to chromosomal aberrations. Lancet, 1: 474475.Google Scholar
Frazer, J., Mitchell, A.J. 1876. Kalmuk idiocy: report of a case with autopsy. With notes on sixty-two cases. J. Mental Sci., 22: 169176.Google Scholar
German, J.L. 1968. Mongolism, delayed fertilization and human sexual behaviour. Nature, 217: 516517.CrossRefGoogle ScholarPubMed
Geyer-Duszynska, I. 1966. Genetic factors in oogenesis and spermatogenesis in Cecidomyidae. Chromosomes Today, 1: 174178.Google Scholar
Grell, R.F. 1971. Distributive pairing in man? Ann. Genet., 14: 165171.Google Scholar
Henderson, S.A., Edwards, R.G. 1968. Chiasma frequency and maternal age in mammals. Nature, 218: 2228.Google Scholar
Henderson, A.S., Warburton, D., Atwood, K.C. 1972. Location of ribosomal DNA in the human chromosome complement. Proc. Natl. Acad. Sci. USA, 69: 33943398.CrossRefGoogle ScholarPubMed
Johnson, R., Strehler, B.L. 1972. Loss of genes coding for rRNA in ageing brain cells. Nature, 240: 412414.Google Scholar
Kahn, J. 1962. The nucleolar organizer in the mitotic chromosome complement of Xenopus laevis. Quart. J. Microscop. Sci., 103: 407410.Google Scholar
Keay, A.J. 1958. The significance of twins in mongolism in the light of new evidence. J. Ment. Defic. Res., 2: 17.Google Scholar
Levkey, A.M., Bell, E., Durnell, J.E. 1963. Ribosomal RNA in the developing chick embryo. Science, 141: 1187.Google Scholar
McDonald, A.D. 1964. Mongolism in twins. J. Med. Genet., 1: 3941.Google Scholar
Mintz, B. 1964. Synthetic processes and early development in the mammalian egg. J. Exptl. Zool., 15785100.Google Scholar
Penrose, L.S. 1933. The relative effects of paternal and maternal age in mongolism. J. Genet. 27: 219223.CrossRefGoogle Scholar
Price, G.V., Modak, S.P., Makinodan, T. 1971. Age-associated changes in the DNA of mouse tissue. Science, 171: 917920.Google Scholar
Raven, C.P. 1961. Oogenesis: the storage of development information. Oxford: Pergamon Press.Google Scholar
Riley, R., Bennett, M.D. 1971. Meiotic DNA synthesis. Nature, 230: 182185.Google Scholar
Salamanca, F., Armendares, S. 1974. C-bands in human metaphase chromosomes treated by barium hydroxide. Ann. Genet., 17: 135137.Google Scholar
Stoller, A., Collman, R.D. 1965. Incidence of infectious hepatitis followed by Down's syndrome nine months later. Lancet, 2: 12211223.Google Scholar
Von Hahn, H.P. 1970. Structural and functional changes in nucleoprotein during the ageing of the cell. Gerontologia, 16: 116118.Google Scholar
Whitehouse, H.L.K., Hastings, P.J. 1965. The analysis of genetic recombination on the polaron hybrid DNA model. Genet. Res., 6: 2792.Google Scholar
Wilson, E.B. 1925. The Cell in Development and Heredity. New York: McMillan.Google Scholar
Wilt, F.H. 1963. The synthesis of ribonucleic acid of the sea urchin embryos. Biochem. Biophys. Res. Commun., 11: 447453.Google Scholar