Spinocerebellar ataxia type 10 (SCA10) is caused by a pentanucleotide repeat expansion of r(AU<u>UCU</u>) within intron 9 of the <i>ATXN10</i> pre-mRNA. The RNA causes disease by a gain-of-function mechanism in which it inactivates proteins involved in RNA biogenesis. Spectroscopic studies showed that r(AU<u>UCU</u>) repeats form a hairpin structure; however, there were no high-resolution structural models prior to this work. Herein, we report the first crystal structure of model r(AU<u>UCU</u>) repeats refined to 2.8 Å and analysis of the structure via molecular dynamics simulations. The r(AU<u>UCU</u>) tracts adopt an overall A-form geometry in which 3 × 3 nucleotide <sup>5′</sup>UCU<sup>3′</sup>/<sup>3′</sup>UCU<sup>5′</sup> internal...
AbstractRNA-protein interactions are essential to a wide range of biological processes. In this pape...
AbstractRNA-protein interactions are essential to a wide range of biological processes. In this pape...
Non-coding RNAs play a pivotal role in a number of diseases promoting an aberrant sequestration of n...
<div><p>In humans, neurodegenerative disorders such as Huntington’s disease (HD) and many spinocereb...
In humans, neurodegenerative disorders such as Huntington's disease (HD) and many spinocerebellar at...
One class of functionally important RNA is repeating transcripts that cause disease through various ...
In humans, neurodegenerative disorders such as Huntington’s disease (HD) and many spi-nocerebellar a...
Myotonic Dystrophy 1 (DM1) is a genetic disease caused by expansion of CTG repeats in DNA. Once tran...
Myotonic Dystrophy 1 (DM1) is a genetic disease caused by expansion of CTG repeats in DNA. Once tran...
Myotonic Dystrophy 1 (DM1) is a genetic disease caused by expansion of CTG repeats in DNA. Once tran...
Myotonic Dystrophy 1 (DM1) is a genetic disease caused by expansion of CTG repeats in DNA. Once tran...
Myotonic Dystrophy 1 (DM1) is a genetic disease caused by expansion of CTG repeats in DNA. Once tran...
The heteronuclear ribonucleoprotein A1 (hnRNPA1 or A1) is associated with the pathology of different...
RNA repeat expansions cause a host of incurable, genetically defined diseases. The most common class...
Mutations in the human tau gene result in alternative splicing of the tau protein, which causes fron...
AbstractRNA-protein interactions are essential to a wide range of biological processes. In this pape...
AbstractRNA-protein interactions are essential to a wide range of biological processes. In this pape...
Non-coding RNAs play a pivotal role in a number of diseases promoting an aberrant sequestration of n...
<div><p>In humans, neurodegenerative disorders such as Huntington’s disease (HD) and many spinocereb...
In humans, neurodegenerative disorders such as Huntington's disease (HD) and many spinocerebellar at...
One class of functionally important RNA is repeating transcripts that cause disease through various ...
In humans, neurodegenerative disorders such as Huntington’s disease (HD) and many spi-nocerebellar a...
Myotonic Dystrophy 1 (DM1) is a genetic disease caused by expansion of CTG repeats in DNA. Once tran...
Myotonic Dystrophy 1 (DM1) is a genetic disease caused by expansion of CTG repeats in DNA. Once tran...
Myotonic Dystrophy 1 (DM1) is a genetic disease caused by expansion of CTG repeats in DNA. Once tran...
Myotonic Dystrophy 1 (DM1) is a genetic disease caused by expansion of CTG repeats in DNA. Once tran...
Myotonic Dystrophy 1 (DM1) is a genetic disease caused by expansion of CTG repeats in DNA. Once tran...
The heteronuclear ribonucleoprotein A1 (hnRNPA1 or A1) is associated with the pathology of different...
RNA repeat expansions cause a host of incurable, genetically defined diseases. The most common class...
Mutations in the human tau gene result in alternative splicing of the tau protein, which causes fron...
AbstractRNA-protein interactions are essential to a wide range of biological processes. In this pape...
AbstractRNA-protein interactions are essential to a wide range of biological processes. In this pape...
Non-coding RNAs play a pivotal role in a number of diseases promoting an aberrant sequestration of n...