نتایج جستجو برای: trinucleotide expansion

تعداد نتایج: 142243  

2016
Yanhao Lai Helen Budworth Jill M. Beaver Nelson L. S. Chan Zunzhen Zhang Cynthia T. McMurray Yuan Liu

Studies in knockout mice provide evidence that MSH2-MSH3 and the BER machinery promote trinucleotide repeat (TNR) expansion, yet how these two different repair pathways cause the mutation is unknown. Here we report the first molecular crosstalk mechanism, in which MSH2-MSH3 is used as a component of the BER machinery to cause expansion. On its own, pol β fails to copy TNRs during DNA synthesis,...

Journal: :Physical chemistry chemical physics : PCCP 2016
Juehan Gao Giel Berden M T Rodgers Jos Oomens

The Watson-Crick structure of DNA is among the most well-known molecular structures of our time. However, alternative base-pairing motifs are also known to occur, often depending on base sequence, pH, or the presence of cations. Pairing of cytosine (C) bases induced by the sharing of a single proton (C-H(+)-C) may give rise to the so-called i-motif, which occurs primarily in expanded trinucleot...

2012
Mark Mühlau Juliane Winkelmann Dan Rujescu Ina Giegling Nikolaos Koutsouleris Christian Gaser Milan Arsic Adolph Weindl Maximilian Reiser Eva M. Meisenzahl

Genetics of the variability of normal and diseased brain structure largely remains to be elucidated. Expansions of certain trinucleotide repeats cause neurodegenerative disorders of which Huntington's disease constitutes the most common example. Here, we test the hypothesis that variation within the IT15 gene on chromosome 4, whose expansion causes Huntington's disease, influences normal human ...

2011
Ganiy Opeyemi Abdulrahman

Trinucleotide repeat disorders are a set of genetic disorders characterized by the expansion of certain genes of a segment of DNA that contains a repeat of three nucleotides, thus exceeding the normal stable threshold. These repeats in the DNA cause repeats of a specific amino acid in the protein sequence, and it is the repeated amino acid that results in a defective protein. Huntington's disea...

Journal: :Cell 1995
Eric N Burright H Brent Clark Antonio Servadio Toni Matilla Rodney M Feddersen Wael S Yunis Lisa A Duvick Huda Y Zoghbi Harry T Orr

Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant inherited disorder characterized by degeneration of cerebellar Purkinje cells, spinocerebellar tracts, and selective brainstem neurons owing to the expansion of an unstable CAG trinucleotide repeat. To gain insight into the pathogenesis of the SCA1 mutation and the intergenerational stability of trinucleotide repeats in mice, we have...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Tao Zu Brian Gibbens Noelle S Doty Mário Gomes-Pereira Aline Huguet Matthew D Stone Jamie Margolis Mark Peterson Todd W Markowski Melissa A C Ingram Zhenhong Nan Colleen Forster Walter C Low Benedikt Schoser Nikunj V Somia H Brent Clark Stephen Schmechel Peter B Bitterman Geneviève Gourdon Maurice S Swanson Melinda Moseley Laura P W Ranum

Trinucleotide expansions cause disease by both protein- and RNA-mediated mechanisms. Unexpectedly, we discovered that CAG expansion constructs express homopolymeric polyglutamine, polyalanine, and polyserine proteins in the absence of an ATG start codon. This repeat-associated non-ATG translation (RAN translation) occurs across long, hairpin-forming repeats in transfected cells or when expansio...

Journal: :genetics in the 3rd millennium 0
الهام خلیلی elham khalili special medical center, tehran, iran مسعود هوشمند masoud houshmand مهدی شفا شریعت پناهی mahdi shafa shariat panahi شهریار نفیسی shahriar nafissi اکبر سلطان زاده akbar soltanzadeh امید آریانی omid ariani

friedreich’s ataxia (fa) is the commonest genetic cause of ataxia and is associated with the expansion of a gaa repeat in intron 1 of the frataxin gene. iron accumulation in the mitochondria of patients with fa results in hypersensitivity to oxidative stress. mitochondrial dna (mtdna) could be considered a candidate modifier factor for fa disease since mitochondrial oxidative stress is thought ...

Journal: :PLoS Genetics 2009
Stéphanie Tomé Ian Holt Winfried Edelmann Glenn E. Morris Arnold Munnich Christopher E. Pearson Geneviève Gourdon

Myotonic dystrophy type 1 (DM1) is associated with one of the most highly unstable CTG*CAG repeat expansions. The formation of further repeat expansions in transgenic mice carrying expanded CTG*CAG tracts requires the mismatch repair (MMR) proteins MSH2 and MSH3, forming the MutSbeta complex. It has been proposed that binding of MutSbeta to CAG hairpins blocks its ATPase activity compromising h...

2012
Eric D. Wieben Ross A. Aleff Nirubol Tosakulwong Malinda L. Butz W. Edward Highsmith Albert O. Edwards Keith H. Baratz

Fuchs endothelial corneal dystrophy (FECD) is a common, familial disease of the corneal endothelium and is the leading indication for corneal transplantation. Variation in the transcription factor 4 (TCF4) gene has been identified as a major contributor to the disease. We tested for an association between an intronic TGC trinucleotide repeat in TCF4 and FECD by determining repeat length in 66 a...

Journal: :Journal of the American Academy of Child and Adolescent Psychiatry 2000
M DiFiglia

Huntington disease (HD) is a neurodegenerative disease that afflicts about 1 in 10,000 individuals. Symptoms include uncontrollable choreiform or dance-like movements, impairment in memory and reasoning ability, and alterations in personality. The average age of onset of symptoms is about 40 years. The symptoms become increasingly disabling with time, and patients die 15 to 20 years after the f...

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