Skip to main content
Log in

A possible cause of non-disjunction of additional chromosome 21 in Down syndrome

  • Published:
Molecular and General Genetics MGG Aims and scope Submit manuscript

Summary

A possible cause of non-disjunction of chromosome 21 in Down Syndromes has been cytogenetically evaluated by examining the parents by Ag-staining technique. In all the cases studied so far, the contributing parents have active ribosomal cistrons on both chromosomes 21 i.e. both chromosomes are stained positively by silver staining. These results show that the active NORs might play an essential role in meiotic non-disjunction. Furthermore, the preliminary results demonstrate that the acrocentric associations of homologous and non-homologous nature involving chromosome 21 are the most frequent in the contributing parent which may further indicate the role of multiple cellular factors affecting the associations in promoting the non-disjunction in addition to active NORs. The possible mechanisms regarding the non-disjunction of chromosome 21 have been described.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Alfi SO, Chang R, Azen PS (1980) Evidence for genetic control of nondisjunction in man. Am J Hum Genet 32:477–483

    Google Scholar 

  • Antonarakis SE, Kittur SD, Metaxotou C, Watkins PC, Patel AS (1985) Analysis of DNA haplotypes suggests genetic predisposition to trisomy 21 associated with DNA sequences on chromosome 21. Proc Natl Acad Sci USA 82:3360–3364

    Google Scholar 

  • Babu KA, Verma RS (1985) Structural and functional aspects of nucleolar organizer regions (NORs) or human chromosomes. Int Rev Cytol 94:151–176

    Google Scholar 

  • de la Cruz FF, Gerald PS (1981) Trisomy 21 (Down Syndromes) research prospective. University Park Press. Baltimore

    Google Scholar 

  • Holmes BL (1978) Genetic counseling for the older pregnant women: new Data and questions. N Engl J Med 298:1419–1921

    Google Scholar 

  • Juberg RC, Mowery PN (1983) Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons. Am J Med Genet 16:111–116

    Google Scholar 

  • Ved Brat S, Verma RS, Dosik H (1979) A simplified technique for simultaneous staining of nucleolar organizer regions (NORs) and kinetochore. Stain Techol 54:107–109

    Google Scholar 

  • Verma RS, Dosik H (1976) An improved method of photographing human fluorescent chromosomes. J Micros 108:339–341

    Google Scholar 

  • Verma RS, Dosik H (1978) Trisomy 21 in a child due to paternal nondisjunction as determined by RFA technique. Jpn J Hum Genet 23:17–21

    Google Scholar 

  • Verma RS, Dosik H (1980) Human chromosomal heteromorphisms. Nature and clinical significance. Int Rev Cytol 62:361–381

    Google Scholar 

  • Verma RS, Lubs HA (1975a) A simple R-banding technic. Am J Hum Genet 27:110–117

    Google Scholar 

  • Verma RS, Lubs HA (1975b) Variation in human acrocentric chromosomes with acridine orange reverse banding. Hum Genet 30:225–235

    Google Scholar 

  • Verma RS, Dosik H, Lubs HA (1977) Demonstration of color and size polymorphisms in human acrocentric chromosomes by acridine orange reverse banding. J Hered 68:262–263

    Google Scholar 

  • Verma RS, Benjamin C, Rodriguez J, Dosik H (1981) Population heteromorphisms of Ag-stained nucleolus organizer regions (NORs) in the acrocentric chromosomes of East Indians. Hum Genet 59:412–415

    Google Scholar 

  • Verma RS, Huq A, Madahar C, Qazi Q, Dosik H (1982a) Higher incidence of small Y chromosome in humans with trisomy 21 (Down Syndrome). Pediatr Res 16:769–770

    Google Scholar 

  • Verma RS, Shah JV, Dosik H (1982b) Orientation of nucleolar organizer chromosomes at somatic metaphases with respect to silver staining. Genetics 100:s 71

    Google Scholar 

  • Verma RS, Shah JV, Dosik H (1983a) Frequencies of chromosome and chromatid types of associations of nucleolar human chromosomes demonstrated by the N-banding technique. Cytobios 36:25–29

    Google Scholar 

  • Verma RS, Rodriguez J, Shah JV, Dosik H (1983b) Preferential association of nucleolar organizing human chromosomes as revealed by silver staining technique at mitosis. Mol Gen Genet 190:352–354

    Google Scholar 

  • Verma RS, Chemitiganti S, Dosik H (1983c) Origin of aneuploid chromosome 21 in Down Syndrome. Genetics 104:s 70

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by R. Illmensee

Rights and permissions

Reprints and permissions

About this article

Cite this article

Verma, R.S., Babu, A., Chemitiganti, S. et al. A possible cause of non-disjunction of additional chromosome 21 in Down syndrome. Molec Gen Genet 202, 339–341 (1986). https://doi.org/10.1007/BF00333259

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00333259

Key words

Navigation