scholarly journals Msh2-Msh3 Interferes with Okazaki Fragment Processing to Promote Trinucleotide Repeat Expansions

Cell Reports ◽  
2012 ◽  
Vol 2 (2) ◽  
pp. 216-222 ◽  
Author(s):  
Athena Kantartzis ◽  
Gregory M. Williams ◽  
Lata Balakrishnan ◽  
Rick L. Roberts ◽  
Jennifer A. Surtees ◽  
...  
Keyword(s):  
Trinucleotide Repeat ◽  
Okazaki Fragment ◽  
Okazaki Fragment Processing ◽  
Repeat Expansions

scholarly journals Patients With Extreme Early Onset Juvenile Huntington Disease Can Have Delays in Diagnosis: A Case Report and Literature Review

2021 ◽  
Vol 8 ◽  
pp. 2329048X2110361
Author(s):  
Ashley A. Moeller ◽  
Marcia V. Felker ◽  
Jennifer A. Brault ◽  
Laura C. Duncan ◽  
Rizwan Hamid ◽  
...  
Keyword(s):  
Symptom Onset ◽  
Huntington Disease ◽  
Early Onset ◽  
Trinucleotide Repeat ◽  
Cerebellar Atrophy ◽  
Cag Repeats ◽  
Ataxic Gait ◽  
Repeat Expansions ◽  
Delays In Diagnosis ◽  
Juvenile Huntington Disease

Huntington disease (HD) is caused by a pathologic cytosine-adenine-guanine (CAG) trinucleotide repeat expansion in the HTT gene. Typical adult-onset disease occurs with a minimum of 40 repeats. With more than 60 CAG repeats, patients can have juvenile-onset disease (jHD), with symptom onset by the age of 20 years. We report a case of a boy with extreme early onset, paternally inherited jHD, with symptom onset between 18 and 24 months. He was found to have 250 to 350 CAG repeats, one of the largest repeat expansions published to date. At initial presentation, he had an ataxic gait, truncal titubation, and speech delay. Magnetic resonance imaging showed cerebellar atrophy. Over time, he continued to regress and became nonverbal, wheelchair-bound, gastrostomy-tube dependent, and increasingly rigid. His young age at presentation and the ethical concerns regarding HD testing in minors delayed his diagnosis.

scholarly journals Creation and Removal of Embedded Ribonucleotides in Chromosomal DNA during Mammalian Okazaki Fragment Processing

1997 ◽  
Vol 272 (36) ◽  
pp. 22591-22599 ◽  
Author(s):  
Jeffrey A. Rumbaugh ◽  
Richard S. Murante ◽  
Shuying Shi ◽  
Robert A. Bambara
Keyword(s):  
Chromosomal Dna ◽  
Okazaki Fragment ◽  
Okazaki Fragment Processing

scholarly journals Twenty-five years since the identification of the first SCA gene: history, clinical features and perspectives for SCA1

2018 ◽  
Vol 76 (8) ◽  
pp. 555-562 ◽  
Author(s):  
Carlos Roberto Martins Junior ◽  
Fabrício Castro de Borba ◽  
Alberto Rolim Muro Martinez ◽  
Thiago Junqueira Ribeiro de Rezende ◽  
Iscia Lopes Cendes ◽  
...  
Keyword(s):  
Clinical Features ◽  
Autosomal Dominant ◽  
Trinucleotide Repeat ◽  
Point Of View ◽  
Spinocerebellar Ataxias ◽  
Coding Region ◽  
The Past ◽  
Monogenic Diseases ◽  
Repeat Expansions ◽  
Core Features

ABSTRACT Spinocerebellar ataxias (SCA) are a clinically and genetically heterogeneous group of monogenic diseases that share ataxia and autosomal dominant inheritance as the core features. An important proportion of SCAs are caused by CAG trinucleotide repeat expansions in the coding region of different genes. In addition to genetic heterogeneity, clinical features transcend motor symptoms, including cognitive, electrophysiological and imaging aspects. Despite all the progress in the past 25 years, the mechanisms that determine how neuronal death is mediated by these unstable expansions are still unclear. The aim of this article is to review, from an historical point of view, the first CAG-related ataxia to be genetically described: SCA 1.

scholarly journals The 26S proteasome drives trinucleotide repeat expansions

2013 ◽  
Vol 41 (12) ◽  
pp. 6098-6108 ◽  
Author(s):  
Claire Concannon ◽  
Robert S. Lahue
Keyword(s):  
Trinucleotide Repeat ◽  
26S Proteasome ◽  
Repeat Expansions

scholarly journals RTEL1 Inhibits Trinucleotide Repeat Expansions and Fragility

Cell Reports ◽  
2014 ◽  
Vol 6 (5) ◽  
pp. 827-835 ◽  
Author(s):  
Aisling Frizzell ◽  
Jennifer H.G. Nguyen ◽  
Mark I.R. Petalcorin ◽  
Katherine D. Turner ◽  
Simon J. Boulton ◽  
...  
Keyword(s):  
Trinucleotide Repeat ◽  
Repeat Expansions

scholarly journals Involvement of Vts1, a structure-specific RNA-binding protein, in Okazaki fragment processing in yeast

2009 ◽  
Vol 38 (5) ◽  
pp. 1583-1595 ◽  
Author(s):  
Chul-Hwan Lee ◽  
Yong-Keol Shin ◽  
Thi Thu Huong Phung ◽  
Jae Seok Bae ◽  
Young-Hoon Kang ◽  
...  
Keyword(s):  
Rna Binding ◽  
Binding Protein ◽  
Rna Binding Protein ◽  
Okazaki Fragment ◽  
Okazaki Fragment Processing
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