Pseudouridines in U2 snRNA stimulate the ATPase activity of Prp5 during spliceosome assembly-Reference-Cited by-同舟云学术

Pseudouridines in U2 snRNA stimulate the ATPase activity of Prp5 during spliceosome assembly

Published:2016-02-12 Issue:6 Volume:35 Page:654-667
ISSN:0261-4189
Container-title:The EMBO Journal
language:en
Short-container-title:EMBO J

Author:

Wu Guowei¹,Adachi Hironori¹,Ge Junhui²,Stephenson David¹,Query Charles C³,Yu Yi‐Tao¹

Affiliation:

1. Department of Biochemistry and Biophysics Center for RNA Biology The Rochester Aging Research (RoAR) Center University of Rochester Medical Center Rochester NY USA

2. Department of Pathology Changzheng Hospital Second Military Medical University Shanghai China

3. Department of Cell Biology Albert Einstein College of Medicine Bronx NY USA

Funder

National Institutes of Health

Publisher

EMBO

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/embj.201593113

Reference45 articles.

1. SLU7 and a novel activity, SSF1, act during the PRP16-dependent step of yeast pre-mRNA splicing.

2. Crystal Structure of Unmodified tRNAGln Complexed with Glutaminyl-tRNA Synthetase and ATP Suggests a Possible Role for Pseudo-Uridines in Stabilization of RNA Structure

3. Mapping of pseudouridine residues in RNA to nucleotide resolution;Bakin AV;Methods Mol Biol,1998

4. A simple and efficient method for direct gene deletion inSaccharomyces cerevisiae

5. The Saccharomyces cerevisiae U2 snRNA:pseudouridine-synthase Pus7p is a novel multisite–multisubstrate RNA:Ψ-synthase also acting on tRNAs

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