Literature DB >> 9718348

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

A E Ashley-Koch1, H Robinson, A E Glicksman, S L Nolin, C E Schwartz, W T Brown, G Turner, S L Sherman.   

Abstract

We examined premutation-female transmissions and premutation-male transmissions of the FMR1 CGG repeat to carrier offspring, to identify factors associated with instability of the repeat. First we investigated associations between parental and offspring repeat size. Premutation-female repeat size was positively correlated with the risk of having full-mutation offspring, confirming previous reports. Similarly, premutation-male repeat size was positively correlated with the daughter's repeat size. However, increasing paternal repeat size was associated also with both increased risk of contraction and decreased magnitude of the repeat-size change passed to the daughter. We hypothesized that the difference between the female and male transmissions was due simply to selection against full-mutation sperm. To test this hypothesis, we simulated selection against full-mutation eggs, by only examining premutation-female transmissions to their premutation offspring. Among this subset of premutation-female transmissions, associations between maternal and offspring repeat size were similar to those observed in premutation-male transmissions. This suggests that the difference between female and male transmissions may be due to selection against full-mutation sperm. Increasing maternal age was associated with increasing risk of expansion to the full mutation, possibly because of selection for smaller alleles within the offspring's soma over time; a similar effect of increasing paternal age may be due to the same selection process. Last, we have evidence that the reported association between offspring sex and risk of expansion may be due to ascertainment bias. Thus, female and male offspring are equally likely to inherit the full mutation.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9718348      PMCID: PMC1377406          DOI: 10.1086/302018

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


  20 in total

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

Authors:  S L Nolin; G E Houck; A D Gargano; H Blumstein; C S Dobkin; W T Brown
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

2.  Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.

Authors:  D C Crawford; C E Schwartz; K L Meadows; J L Newman; L F Taft; C Gunter; W T Brown; N J Carpenter; P N Howard-Peebles; K G Monaghan; S L Nolin; A L Reiss; G L Feldman; E M Rohlfs; S T Warren; S L Sherman
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

3.  Longitudinal interviews of couples diagnosed with diminished ovarian reserve undergoing fragile X premutation testing.

Authors:  Lisa M Pastore; Logan B Karns; Karen Ventura; Myra L Clark; Richard H Steeves; Nancy Callanan
Journal:  J Genet Couns       Date:  2013-06-14       Impact factor: 2.537

Review 4.  Fragile sites-cytogenetic similarity with molecular diversity.

Authors:  G R Sutherland; R I Richards
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

Review 5.  On the wrong DNA track: Molecular mechanisms of repeat-mediated genome instability.

Authors:  Alexandra N Khristich; Sergei M Mirkin
Journal:  J Biol Chem       Date:  2020-02-14       Impact factor: 5.157

6.  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

7.  FMR1 CGG expansions: prevalence and sex ratios.

Authors:  Matthew J Maenner; Mei W Baker; Karl W Broman; Jianan Tian; Janel K Barnes; Anne Atkins; Elizabeth McPherson; Jinkuk Hong; Murray H Brilliant; Marsha R Mailick
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2013-06-05       Impact factor: 3.568

8.  Somatic expansion in mouse and human carriers of fragile X premutation alleles.

Authors:  Rachel Adihe Lokanga; Ali Entezam; Daman Kumari; Dmitry Yudkin; Mei Qin; Carolyn Beebe Smith; Karen Usdin
Journal:  Hum Mutat       Date:  2012-10-04       Impact factor: 4.878

9.  Huntington disease expansion mutations in humans can occur before meiosis is completed.

Authors:  Song-Ro Yoon; Louis Dubeau; Margot de Young; Nancy S Wexler; Norman Arnheim
Journal:  Proc Natl Acad Sci U S A       Date:  2003-07-11       Impact factor: 11.205

10.  Translation of the FMR1 mRNA is not influenced by AGG interruptions.

Authors:  Anna L Ludwig; Christopher Raske; Flora Tassone; Dolores Garcia-Arocena; John W Hershey; Paul J Hagerman
Journal:  Nucleic Acids Res       Date:  2009-09-14       Impact factor: 16.971

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.