» Articles » PMID: 6232199

Cytogenetic Investigations in Mentally Retarded and Normal Males from 14 Families with the Fragile Site at Xq28. Results of Folic Acid Treatment on Fra(X) Expression

Overview
Journal Hum Genet
Specialty Genetics
Date 1984 Jan 1
PMID 6232199
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Lymphocyte cultures from 27 mentally retarded males aged 1 year to 77 years, and from 11 normal brothers from a total of 14 families with the fragile X segregating have been examined cytogenetically employing three different culture methods including methods for induction of fra(X) by FUdR (flourodeoxyuridine) or MTX (methotrexate). All mentally retarded males showed unequivocal fra(X) expression. No statistically significant correlation between fra(X) expression and age could be demonstrated. No enhancement with FUdR was observed. Fibroblast cultures from 10 retarded males expressed fra(X) in a dose-response relationship to increasing concentrations of FUdR. None of the normal males showed fra(X). In vivo folic acid treatment of seven mentally retarded males resulted in marked reduction in fra(X) expression in lymphocyte cultures grown in medium 199. However, reinduction was achieved by FUdR or MTX, except in one case who temporarily received very high doses of folic acid.

Citing Articles

A set of male monozygotic triplets with schizophrenic psychoses: nature or nurture?.

Harnryd C, Jonsson E, Greitz D, Nyman H, Sedvall G Eur Arch Psychiatry Clin Neurosci. 1995; 245(1):1-7.

PMID: 7786906 DOI: 10.1007/BF02191537.


The role of fluorinated pyrimidine analogues in the induction of the in vitro expression of the fragile X chromosome.

Vandamme B, Liebaers I, Hens L, Bernheim J, Roobol C Hum Genet. 1988; 79(4):341-6.

PMID: 2970425 DOI: 10.1007/BF00282173.


The fragile X mutation does not have any major effect on the expression of the hypoxanthine phosphoribosyltransferase (HPRT) locus in human fibroblasts.

Steen A, MARCUS S, Sahlen S, NIELSEN K, Lambert B Hum Genet. 1991; 87(4):503-5.

PMID: 1715310 DOI: 10.1007/BF00197177.

References
1.
Brookwell R, Daniel A, Turner G, Fishburn J . The fragile X(q27) form of X-linked mental retardation: FUdR as an inducing agent for fra(X)(q27) expression in lymphocytes, fibroblasts, and amniocytes. Am J Med Genet. 1982; 13(2):139-48. DOI: 10.1002/ajmg.1320130206. View

2.
Turner G, Daniel A, Frost M . X-linked mental retardation, macro-orchidism, and the Xq27 fragile site. J Pediatr. 1980; 96(5):837-41. DOI: 10.1016/s0022-3476(80)80552-x. View

3.
Nielsen L, NIELSEN K, Tommerup N . Fragile X demonstrated retrospectively in amniotic cells cultured in low folate medium. Prenat Diagn. 1983; 3(4):367-9. DOI: 10.1002/pd.1970030417. View

4.
NIELSEN K, Tommerup N, POULSEN H, Jacobsen P, Beck B, Mikkelsen M . Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile X. Hum Genet. 1983; 64(3):240-5. DOI: 10.1007/BF00279401. View

5.
Sherman S, Morton N, Jacobs P, Turner G . The marker (X) syndrome: a cytogenetic and genetic analysis. Ann Hum Genet. 1984; 48(1):21-37. DOI: 10.1111/j.1469-1809.1984.tb00830.x. View