Literature DB >> 25210937

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

Sarah L Nolin1, Anne Glicksman1, Nicole Ersalesi1, Carl Dobkin1, W Ted Brown1, Ru Cao2, Eliot Blatt2, Sachin Sah2, Gary J Latham2, Andrew G Hadd2.   

Abstract

PURPOSE: Fragile X CGG repeat alleles often contain one or more AGG interruptions that influence allele stability and risk of a full mutation transmission from parent to child. We have examined transmissions of maternal and paternal alleles with 45-90 repeats to quantify the effect of AGG interruptions on fragile X repeat instability.
METHODS: A novel FMR1 polymerase chain reaction assay was used to determine CGG repeat length and AGG interruptions for 1,040 alleles from 705 families.
RESULTS: We grouped transmissions into nine categories of five repeats by parental size and found that in every size category, alleles with no AGGs had the greatest risk for instability. For maternal alleles <75 repeats, 89% (24/27) that expanded to a full mutation had no AGGs. Two contractions in maternal transmission were accompanied by loss of AGGs, suggesting a mechanism for generating alleles that lack AGG interruptions. Maternal age was examined as a factor in full mutation expansions using prenatal samples to minimize ascertainment bias, and a possible effect was observed though it was not statistically significant (P = 0.06).
CONCLUSION: These results strengthen the association of AGG repeats with CGG repeat stability and provide more accurate risk estimates of full mutation expansions for women with 45-90 repeat alleles.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 25210937     DOI: 10.1038/gim.2014.106

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  22 in total

1.  Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR.

Authors:  D C Crawford; B Wilson; S L Sherman
Journal:  Hum Mol Genet       Date:  2000-11-22       Impact factor: 6.150

2.  Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome.

Authors:  I Oberlé; F Rousseau; D Heitz; C Kretz; D Devys; A Hanauer; J Boué; M F Bertheas; J L Mandel
Journal:  Science       Date:  1991-05-24       Impact factor: 47.728

Review 3.  Repeat instability: mechanisms of dynamic mutations.

Authors:  Christopher E Pearson; Kerrie Nichol Edamura; John D Cleary
Journal:  Nat Rev Genet       Date:  2005-10       Impact factor: 53.242

Review 4.  Intraclass correlations: uses in assessing rater reliability.

Authors:  P E Shrout; J L Fleiss
Journal:  Psychol Bull       Date:  1979-03       Impact factor: 17.737

5.  Expansion of an FMR1 grey-zone allele to a full mutation in two generations.

Authors:  Isabel Fernandez-Carvajal; Blanca Lopez Posadas; Ruiqin Pan; Christopher Raske; Paul J Hagerman; Flora Tassone
Journal:  J Mol Diagn       Date:  2009-06-12       Impact factor: 5.568

6.  Length of uninterrupted CGG repeats determines instability in the FMR1 gene.

Authors:  E E Eichler; J J Holden; B W Popovich; A L Reiss; K Snow; S N Thibodeau; C S Richards; P A Ward; D L Nelson
Journal:  Nat Genet       Date:  1994-09       Impact factor: 38.330

7.  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

8.  Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females.

Authors:  S L Sherman; K L Meadows; A E Ashley
Journal:  Am J Med Genet       Date:  1996-08-09

9.  Promoter-bound trinucleotide repeat mRNA drives epigenetic silencing in fragile X syndrome.

Authors:  Dilek Colak; Nikica Zaninovic; Michael S Cohen; Zev Rosenwaks; Wang-Yong Yang; Jeannine Gerhardt; Matthew D Disney; Samie R Jaffrey
Journal:  Science       Date:  2014-02-28       Impact factor: 47.728

10.  Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis.

Authors:  Amy Cronister; Jennifer Teicher; Elizabeth M Rohlfs; Alan Donnenfeld; Stephanie Hallam
Journal:  Obstet Gynecol       Date:  2008-03       Impact factor: 7.661

View more
  53 in total

1.  Mutsβ generates both expansions and contractions in a mouse model of the Fragile X-associated disorders.

Authors:  Xiao-Nan Zhao; Daman Kumari; Shikha Gupta; Di Wu; Maya Evanitsky; Wei Yang; Karen Usdin
Journal:  Hum Mol Genet       Date:  2015-09-29       Impact factor: 6.150

Review 2.  Advanced technologies for the molecular diagnosis of fragile X syndrome.

Authors:  Flora Tassone
Journal:  Expert Rev Mol Diagn       Date:  2015-10-21       Impact factor: 5.225

3.  Molecular Characterization of FMR1 Gene by TP-PCR in Women of Reproductive Age and Women with Premature Ovarian Insufficiency.

Authors:  Deepika Delsa Dean; Sarita Agarwal; Deepa Kapoor; Kuldeep Singh; Chandra Vati
Journal:  Mol Diagn Ther       Date:  2018-02       Impact factor: 4.074

4.  Improving Health Education for Women Who Carry an FMR1 Premutation.

Authors:  Whitney Espinel; Krista Charen; Lillie Huddleston; Jeannie Visootsak; Stephanie Sherman
Journal:  J Genet Couns       Date:  2015-07-16       Impact factor: 2.537

Review 5.  Does theFMR1 gene affect IVF success?

Authors:  Lisa M Pastore; Mindy S Christianson; Bailey McGuinness; Kamaria Cayton Vaught; Jacqueline Y Maher; William G Kearns
Journal:  Reprod Biomed Online       Date:  2018-12-10       Impact factor: 3.828

6.  A Set of Assays for the Comprehensive Analysis of FMR1 Alleles in the Fragile X-Related Disorders.

Authors:  Bruce E Hayward; Yifan Zhou; Daman Kumari; Karen Usdin
Journal:  J Mol Diagn       Date:  2016-08-12       Impact factor: 5.568

7.  Improved Assays for AGG Interruptions in Fragile X Premutation Carriers.

Authors:  Bruce E Hayward; Karen Usdin
Journal:  J Mol Diagn       Date:  2017-08-14       Impact factor: 5.568

8.  Health knowledge of women with a fragile X premutation: Improving understanding with targeted educational material.

Authors:  Liana Smolich; Krista Charen; Stephanie L Sherman
Journal:  J Genet Couns       Date:  2020-01-30       Impact factor: 2.537

Review 9.  Recent advances in assays for the fragile X-related disorders.

Authors:  Bruce E Hayward; Daman Kumari; Karen Usdin
Journal:  Hum Genet       Date:  2017-09-02       Impact factor: 4.132

10.  Does the presence of AGG interruptions within the CGG repeat tract have a protective effect on the fertility phenotype of female FMR1 premutation carriers?

Authors:  M Friedman-Gohas; M Kirshenbaum; A Michaeli; N Domniz; S Elizur; H Raanani; R Orvieto; Y Cohen
Journal:  J Assist Reprod Genet       Date:  2020-02-24       Impact factor: 3.412

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.