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PMID: 3785381 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Implications of fragile X expression in normal males for the nature of the mutation.

Nature ·Vol. 324 ·No. 6093 ·1986-00-00 ·Pages 161-3

Ledbetter DH, Ledbetter SA, Nussbaum RL

Abstract

The fragile site at Xq27, associated with a common form of X-linked mental retardation (XLMR), is expressed in a variable proportion of the peripheral lymphocytes of affected males when the cells are cultured under thymidylate stress (Td stress) produced by folate or thymidylate deprivation. Some clinically normal males--transmitting males--are known to carry and transmit the fragile X mutation and yet show no cytogenetic expression in lymphocytes. Normal males with no family history of X-linked mental retardation express the site only rarely. When the fragile X chromosome from affected males is isolated in a rodent genetic background by somatic cell hybridization, the level of expression is similar to that seen in lymphocytes under Td stress. Here we show that X chromosomes from two transmitting males and two normal control males, all of which were fragile X negative in lymphocytes or lymphoblasts, could be made to express the fragile site in hybrids, although at levels that were below those seen in hybrids from affected males. Furthermore, transmitting males could be differentiated from normal males by their significantly higher expression rates when hybrids were exposed to caffeine before cytogenetic harvest. One male chimpanzee also showed low level expression in hybrid cells. These data suggest that the hybrid system lowers the threshold for fragile X expression, a fragile site at Xq27 may be present on all human and chimpanzee X chromosomes and constitutes a previously unrecognized common fragile site and the hybrid system with caffeine post-treatment can distinguish between the common Xq27 fragile site of control males, the occult mutant fragile site of a transmitting male, and the fully expressed fragile site of an affected male with XLMR. Thus the mutation producing XLMR may represent a multi-step alteration of a naturally occurring DNA sequence producing a continuum of cytogenetic expression and a threshold for clinical manifestation.

MeSH Terms
Animals Caffeine/pharmacology Fragile X Syndrome/genetics Gene Expression Regulation/drug effects Humans Hybrid Cells/physiology Intellectual Disability/genetics Male Pan troglodytes/genetics Sex Chromosome Aberrations/genetics Thymidine/metabolism X Chromosome
Chemicals
Caffeine Thymidine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ledbetter D H
Ledbetter S A
Nussbaum R L
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1986-00-00
Pages
161-3
Language
English
Region
England
NLM ID
0410462
Subset
IM
Grants
NICHD NIH HHS · R01 HD20227 · United States
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