Literature DB >> 12952862

A fragile balance: FMR1 expression levels.

Ben A Oostra1, Rob Willemsen.   

Abstract

The FMR1 gene is involved in three different syndromes, the Fragile X syndrome, premature ovarian failure (POF) and the Fragile X-associated tremor/ataxia syndrome (FXTAS) at older age. Fragile X syndrome is caused by an expanded CGG repeat above 200 units in the FMR1 gene resulting in the absence of the FMR1 mRNA and protein. The FMR1 protein is proposed to act as a regulator of mRNA transport and/or translation that plays a role in synaptic maturation and function. POF and FXTAS are found in individuals with an expanded repeat between 50 and 200 CGGs and are associated with increased FMR1 mRNA levels. The presence of elevated FMR1 mRNA in all patients suggests that these syndromes may represent a gain-of-function effect from the elevated message levels. The level of FMR1 mRNA is in fragile balance and is therefore critical for normal functioning.

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Year:  2003        PMID: 12952862     DOI: 10.1093/hmg/ddg298

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  50 in total

Review 1.  The impact of FMR1 gene mutations on human reproduction and development: a systematic review.

Authors:  Vincenzo Noto; Conor Harrity; David Walsh; Kevin Marron
Journal:  J Assist Reprod Genet       Date:  2016-07-18       Impact factor: 3.412

2.  Autism Symptomatology in Boys with Fragile X Syndrome: A Cross Sectional Developmental Trajectories Comparison with Nonsyndromic Autism Spectrum Disorder.

Authors:  Angela John Thurman; Andrea McDuffie; Sara T Kover; Randi J Hagerman; Leonard Abbeduto
Journal:  J Autism Dev Disord       Date:  2015-09

3.  Language Skills of Males with Fragile X Syndrome or Nonsyndromic Autism Spectrum Disorder.

Authors:  Angela John Thurman; Andrea McDuffie; Randi J Hagerman; Cynde K Josol; Leonard Abbeduto
Journal:  J Autism Dev Disord       Date:  2017-03

4.  Use of emotional cues for lexical learning: a comparison of autism spectrum disorder and fragile X syndrome.

Authors:  Angela John Thurman; Andrea McDuffie; Sara T Kover; Randi Hagerman; Marie Moore Channell; Ann Mastergeorge; Leonard Abbeduto
Journal:  J Autism Dev Disord       Date:  2015-04

5.  Correlation of normal-range FMR1 repeat length or genotypes and reproductive parameters.

Authors:  Bat-Sheva L Maslow; Stephanie Davis; Lawrence Engmann; John C Nulsen; Claudio A Benadiva
Journal:  J Assist Reprod Genet       Date:  2016-05-17       Impact factor: 3.412

Review 6.  Partners in crime: bidirectional transcription in unstable microsatellite disease.

Authors:  Ranjan Batra; Konstantinos Charizanis; Maurice S Swanson
Journal:  Hum Mol Genet       Date:  2010-04-04       Impact factor: 6.150

7.  Side effects of minocycline treatment in patients with fragile X syndrome and exploration of outcome measures.

Authors:  Agustini Utari; Weerasak Chonchaiya; Susan M Rivera; Andrea Schneider; Randi J Hagerman; Sultana M H Faradz; Iryna M Ethell; Danh V Nguyen
Journal:  Am J Intellect Dev Disabil       Date:  2010-09

Review 8.  FXTAS: a progressive neurologic syndrome associated with Fragile X premutation.

Authors:  Rob Willemsen; Edwin Mientjes; Ben A Oostra
Journal:  Curr Neurol Neurosci Rep       Date:  2005-09       Impact factor: 5.081

Review 9.  Fragile X syndrome: the FMR1 CGG repeat distribution among world populations.

Authors:  Emmanuel Peprah
Journal:  Ann Hum Genet       Date:  2011-12-21       Impact factor: 1.670

10.  Elevated FMR1 mRNA in premutation carriers is due to increased transcription.

Authors:  Flora Tassone; Alexandra Beilina; Chiara Carosi; Serena Albertosi; Claudia Bagni; Lexin Li; Kira Glover; David Bentley; Paul J Hagerman
Journal:  RNA       Date:  2007-02-05       Impact factor: 4.942

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