Literature DB >> 10441574

FMR1 CGG-repeat instability in single sperm and lymphocytes of fragile-X premutation males.

S L Nolin1, G E Houck, A D Gargano, H Blumstein, C S Dobkin, W T Brown.   

Abstract

To determine the meiotic instability of the CGG-triplet repeat in the fragile-X gene, FMR1, we examined the size of the repeat in single sperm from four premutation males. The males had CGG-repeat sizes of 68, 75, 78, and 100, as determined in peripheral blood samples. All samples showed a broad range of variations, with expansions more common than contractions. Examination of single lymphocytes indicated that somatic cells were relatively more stable than sperm. Surprisingly, the repeats in sperm from the 75- and 78-repeat males had very different size ranges and distribution patterns despite the similarity of the repeat size and AGG interruption in their somatic cells. These results suggest that cis or trans factors may have a role in male germline repeat instability.

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Year:  1999        PMID: 10441574      PMCID: PMC1377974          DOI: 10.1086/302543

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  47 in total

1.  Examination of factors associated with instability of the FMR1 CGG repeat.

Authors:  A E Ashley-Koch; H Robinson; A E Glicksman; S L Nolin; C E Schwartz; W T Brown; G Turner; S L Sherman
Journal:  Am J Hum Genet       Date:  1998-09       Impact factor: 11.025

2.  Analysis of germline variation at the FMR1 CGG repeat shows variation in the normal-premutated borderline range.

Authors:  E Mornet; C Chateau; M C Hirst; F Thepot; A Taillandier; O Cibois; J L Serre
Journal:  Hum Mol Genet       Date:  1996-06       Impact factor: 6.150

3.  Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation.

Authors:  K Snow; D J Tester; K E Kruckeberg; D J Schaid; S N Thibodeau
Journal:  Hum Mol Genet       Date:  1994-09       Impact factor: 6.150

4.  Improved sizing of fragile X CCG repeats by nested polymerase chain reaction.

Authors:  G Levinson; A Maddalena; F T Palmer; G L Harton; D P Bick; P N Howard-Peebles; S H Black; J D Schulman
Journal:  Am J Med Genet       Date:  1994-07-15

5.  CAG repeat length variation in sperm from a patient with Kennedy's disease.

Authors:  L Zhang; K H Fischbeck; N Arnheim
Journal:  Hum Mol Genet       Date:  1995-02       Impact factor: 6.150

6.  FRAXE mutation analysis in three Spanish families.

Authors:  P Carbonell; I López; J Gabarrón; M J Bernabé; J M Lucas; M Guitart; E Gabau; G Glover
Journal:  Am J Med Genet       Date:  1996-08-09

7.  Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses.

Authors:  D G Monckton; L J Wong; T Ashizawa; C T Caskey
Journal:  Hum Mol Genet       Date:  1995-01       Impact factor: 6.150

8.  Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum.

Authors:  E P Leeflang; L Zhang; S Tavaré; R Hubert; J Srinidhi; M E MacDonald; R H Myers; M de Young; N S Wexler; J F Gusella
Journal:  Hum Mol Genet       Date:  1995-09       Impact factor: 6.150

9.  The fragile X premutation in carriers and its effect on mutation size in offspring.

Authors:  G S Fisch; K Snow; S N Thibodeau; M Chalifaux; J J Holden; D L Nelson; P N Howard-Peebles; A Maddalena
Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025

10.  Fragile X gene instability: anchoring AGGs and linked microsatellites.

Authors:  N Zhong; W Yang; C Dobkin; W T Brown
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

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  14 in total

1.  CpG methylation modifies the genetic stability of cloned repeat sequences.

Authors:  Kerrie Nichol; Christopher E Pearson
Journal:  Genome Res       Date:  2002-08       Impact factor: 9.043

2.  Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size range.

Authors:  Amy K Sullivan; Dana C Crawford; Elizabeth H Scott; Mary L Leslie; Stephanie L Sherman
Journal:  Am J Hum Genet       Date:  2002-05-03       Impact factor: 11.025

3.  Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations?

Authors:  U Salat; B Bardoni; D Wöhrle; P Steinbach
Journal:  J Med Genet       Date:  2000-11       Impact factor: 6.318

4.  Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles.

Authors:  Sarah L Nolin; Sachin Sah; Anne Glicksman; Stephanie L Sherman; Emily Allen; Elizabeth Berry-Kravis; Flora Tassone; Carolyn Yrigollen; Amy Cronister; Marcia Jodah; Nicole Ersalesi; Carl Dobkin; W Ted Brown; Raghav Shroff; Gary J Latham; Andrew G Hadd
Journal:  Am J Med Genet A       Date:  2013-02-26       Impact factor: 2.802

5.  CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles.

Authors:  Dalyir I Pretto; Guadalupe Mendoza-Morales; Joyce Lo; Ru Cao; Andrew Hadd; Gary J Latham; Blythe Durbin-Johnson; Randi Hagerman; Flora Tassone
Journal:  J Med Genet       Date:  2014-03-03       Impact factor: 6.318

6.  MSH2-dependent germinal CTG repeat expansions are produced continuously in spermatogonia from DM1 transgenic mice.

Authors:  Cédric Savouret; Corinne Garcia-Cordier; Jérôme Megret; Hein te Riele; Claudine Junien; Geneviève Gourdon
Journal:  Mol Cell Biol       Date:  2004-01       Impact factor: 4.272

Review 7.  FMR1 and the fragile X syndrome: human genome epidemiology review.

Authors:  D C Crawford; J M Acuña; S L Sherman
Journal:  Genet Med       Date:  2001 Sep-Oct       Impact factor: 8.822

Review 8.  The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspective.

Authors:  Gary J Latham; Justine Coppinger; Andrew G Hadd; Sarah L Nolin
Journal:  Front Genet       Date:  2014-07-29       Impact factor: 4.599

9.  Of Men and Mice: Modeling the Fragile X Syndrome.

Authors:  Regina Dahlhaus
Journal:  Front Mol Neurosci       Date:  2018-03-15       Impact factor: 5.639

10.  Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers.

Authors:  Sarah L Nolin; Anne Glicksman; Nicole Ersalesi; Carl Dobkin; W Ted Brown; Ru Cao; Eliot Blatt; Sachin Sah; Gary J Latham; Andrew G Hadd
Journal:  Genet Med       Date:  2014-09-11       Impact factor: 8.822

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