Home LiteratureArticle Details
PMID: 7874164 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.

Nature genetics ·Vol. 8 ·No. 3 ·1994-11-00 ·Pages 229-35

Parrish JE, Oostra BA, Verkerk AJ, Richards CS, Reynolds J, Spikes AS, Shaffer LG, Nelson DL

Abstract

Three folate-sensitive fragile sites, termed FRAXA, FRAXE and FRAXF, have been identified on the distal end of chromosome Xq. The first two contain expanded, hypermethylated and unstable CGG (or GCC) repeats within CpG islands. We now report the isolation of similar sequences responsible for the third fragile site, FRAXF. A 5-kilobase EcoRI fragment derived from a cosmid coincident with the cytogenetic anomaly detects expanded, methylated and unstable sequences in five individuals who exhibit fragile sites in distal Xq; these individuals have normal repeat lengths at both FRAXA and FRAXE. By sequence analysis, the expanded region contains a GCC repeat. PCR and sequence analysis of chromosomes from the general population indicates that the repeat is polymorphic (6 to 29 triplets), and is stable upon transmission.

Related Genes
MeSH Terms
Alleles Animals Base Sequence Chromosome Fragile Sites Chromosome Fragility Cricetinae Female Fragile X Syndrome/genetics Genetic Markers Humans Male Methylation Mice Minisatellite Repeats Molecular Sequence Data Pedigree X Chromosome/ultrastructure
Chemicals
Genetic Markers
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Parrish J E
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030.
Oostra B A
Verkerk A J
Richards C S
Reynolds J
Spikes A S
Shaffer L G
Nelson D L
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
Published
1994-11-00
Pages
229-35
Language
English
Region
United States
NLM ID
9216904
Subset
IM
Grants
NHGRI NIH HHS · 5P30 HG00210 · United States
NICHD NIH HHS · 5R01 HD29256-02 · United States
Databases
GENBANK
L35600
Corrections
CommentIn
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