نتایج جستجو برای: splicing modulation

تعداد نتایج: 176802  

2015
Min Zheng Pui Wang Wenjun Song Siu-Ying Lau Siwen Liu Xiaofeng Huang Bobo Wing-Yee Mok Yen-Chin Liu Yixin Chen Kwok-Yung Yuen Honglin Chen A. García-Sastre

UNLABELLED The NS1 protein of influenza virus has multiple functions and is a determinant of virulence. Influenza viruses with NS1 deletions (DelNS1 influenza viruses) are a useful tool for studying virus replication and can serve as effective live attenuated vaccines, but deletion of NS1 severely diminishes virus replication, hampering functional studies and vaccine production. We found that W...

Journal: :Human molecular genetics 2012
Seth J Brown Peter Stoilov Yi Xing

New data are revealing a complex landscape of gene regulation shaped by chromatin states that extend into the bodies of transcribed genes and associate with distinct RNA elements such as exons, introns and polyadenylation sites. Exons are characterized by increased levels of nucleosome positioning, DNA methylation and certain histone modifications. As pre-mRNA splicing occurs co-transcriptional...

Journal: :Nucleic acids research 1997
K Savitsky M Platzer T Uziel S Gilad A Sartiel A Rosenthal O Elroy-Stein Y Shiloh G Rotman

Mutations in the ATM gene are responsible for the multisystem disorder ataxia-telangiectasia, characterized by neurodegeneration, immune deficiency and cancer predisposition. While no alternative splicing was identified within the coding region, the first four exons of the ATM gene, which fall within the 5'untranslated region (UTR), undergo extensive alternative splicing. We identified 12 diffe...

2017
Daniel Cirera-Salinas Jian Yu Maxime Bodak Richard P Ngondo Kristina M Herbert Constance Ciaudo

Mouse embryonic stem cells (mESCs) deficient for DGCR8, a key component of the microprocessor complex, present strong differentiation defects. However, the exact reasons impairing their commitment remain elusive. The analysis of newly generated mutant mESCs revealed that DGCR8 is essential for the exit from the pluripotency state. To dissociate canonical versus noncanonical functions of DGCR8, ...

Journal: :Nature chemical biology 2015
James Palacino Susanne E Swalley Cheng Song Atwood K Cheung Lei Shu Xiaolu Zhang Mailin Van Hoosear Youngah Shin Donovan N Chin Caroline Gubser Keller Martin Beibel Nicole A Renaud Thomas M Smith Michael Salcius Xiaoying Shi Marc Hild Rebecca Servais Monish Jain Lin Deng Caroline Bullock Michael McLellan Sven Schuierer Leo Murphy Marcel J J Blommers Cecile Blaustein Frada Berenshteyn Arnaud Lacoste Jason R Thomas Guglielmo Roma Gregory A Michaud Brian S Tseng Jeffery A Porter Vic E Myer John A Tallarico Lawrence G Hamann Daniel Curtis Mark C Fishman William F Dietrich Natalie A Dales Rajeev Sivasankaran

Spinal muscular atrophy (SMA), which results from the loss of expression of the survival of motor neuron-1 (SMN1) gene, represents the most common genetic cause of pediatric mortality. A duplicate copy (SMN2) is inefficiently spliced, producing a truncated and unstable protein. We describe herein a potent, orally active, small-molecule enhancer of SMN2 splicing that elevates full-length SMN pro...

2016
Joanna Y. Ip Masamitsu Sone Chieko Nashiki Qun Pan Kiyoyuki Kitaichi Kaori Yanaka Takaya Abe Keizo Takao Tsuyoshi Miyakawa Benjamin J. Blencowe Shinichi Nakagawa

The long noncoding RNA Gomafu/MIAT/Rncr2 is thought to function in retinal cell specification, stem cell differentiation and the control of alternative splicing. To further investigate physiological functions of Gomafu, we created mouse knockout (KO) model that completely lacks the Gomafu gene. The KO mice did not exhibit any developmental deficits. However, behavioral tests revealed that the K...

Journal: :Nature medicine 2018
Michael Seiler Akihide Yoshimi Rachel Darman Betty Chan Gregg Keaney Michael Thomas Anant A Agrawal Benjamin Caleb Alfredo Csibi Eckley Sean Peter Fekkes Craig Karr Virginia Klimek George Lai Linda Lee Pavan Kumar Stanley Chun-Wei Lee Xiang Liu Crystal Mackenzie Carol Meeske Yoshiharu Mizui Eric Padron Eunice Park Ermira Pazolli Shouyong Peng Sudeep Prajapati Justin Taylor Teng Teng John Wang Markus Warmuth Huilan Yao Lihua Yu Ping Zhu Omar Abdel-Wahab Peter G Smith Silvia Buonamici

Genomic analyses of cancer have identified recurrent point mutations in the RNA splicing factor-encoding genes SF3B1, U2AF1, and SRSF2 that confer an alteration of function. Cancer cells bearing these mutations are preferentially dependent on wild-type (WT) spliceosome function, but clinically relevant means to therapeutically target the spliceosome do not currently exist. Here we describe an o...

2017
Atsushi Takata Naomichi Matsumoto Tadafumi Kato

Detailed analyses of transcriptome have revealed complexity in regulation of alternative splicing (AS). These AS events often undergo modulation by genetic variants. Here we analyse RNA-sequencing data of prefrontal cortex from 206 individuals in combination with their genotypes and identify cis-acting splicing quantitative trait loci (sQTLs) throughout the genome. These sQTLs are enriched amon...

2017
Ivano Legnini Gaia Di Timoteo Francesca Rossi Mariangela Morlando Francesca Briganti Olga Sthandier Alessandro Fatica Tiziana Santini Adrian Andronache Mark Wade Pietro Laneve Nikolaus Rajewsky Irene Bozzoni

Circular RNAs (circRNAs) constitute a family of transcripts with unique structures and still largely unknown functions. Their biogenesis, which proceeds via a back-splicing reaction, is fairly well characterized, whereas their role in the modulation of physiologically relevant processes is still unclear. Here we performed expression profiling of circRNAs during in vitro differentiation of murin...

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