People

Jonathan P. Staley, PhD

  • Chair of Molecular Genetics and Cell Biology
    Professor of Molecular Genetics and Cell Biology
    Committee on Genetics, Genomics and Systems Biology
  • Research and Scholarly Interests: ATPase, Baker's Yeast, Brewer's Yeast, cotranscriptional processes, DEAD-box RNA Helicases, DEAH-box RNA helicase, Exon, Gene Expression Regulation, genome-wide studies, Intron, mammalian proteins, mammalian systems, Messenger RNA, Nuclear Export, Pre-mRNA, RNA, RNA dependent ATPase, RNA Helicase, RNA Sequence, snRNA, Spliceosome, splicing, Yeast Proteins
  • Websites: Staley Lab Website, Research Network Profile
  • Contact: jstaley@uchicago.edu
  • Graduate Programs: Cell & Molecular Biology, Genetics, Genomics & Systems Biology, UChicago Biosciences

Our goal is to understand the mechanism and regulation of nuclear pre-mRNA splicing, an essential step in eukaryotic gene expression. Pre-mRNA splicing is catalyzed by a massive multimegadalton ribonucleoprotein machine called the spliceosome. Using the model organism S. cerevisiae as well as human cells, we apply a wide array of approaches, ranging from single molecule microscopy, biophysics, and chemical biology to biochemistry and cell biology to genetics and genomics to gain a deep understanding of how the spliceosome catalyzes and regulates pre-mRNA splicing, including in the context of transcription.

University of California at San Francisco (Advisor: Christine Guthrie)
San Francisco, CA
Postdoc - Biochemistry/Genetics
1999

Massachusetts Institute of Technology (Advisor: Peter S. Kim)
Boston, MA
Ph.D. - Chemistry/Biophysics
1993

Haverford College
Haverford, PA
B.A. - Chemistry
1987

Global impact of aberrant splicing on human gene expression levels.
Global impact of aberrant splicing on human gene expression levels. bioRxiv. 2023 Oct 16.
PMID: 37745605

The debranching enzyme Dbr1 regulates lariat turnover and intron splicing.
The debranching enzyme Dbr1 regulates lariat turnover and intron splicing. Res Sq. 2023 Jun 13.
PMID: 37398028

Profiling lariat intermediates reveals genetic determinants of early and late co-transcriptional splicing.
Profiling lariat intermediates reveals genetic determinants of early and late co-transcriptional splicing. Mol Cell. 2022 12 15; 82(24):4681-4699.e8.
PMID: 36435176

Termination of pre-mRNA splicing requires that the ATPase and RNA unwindase Prp43p acts on the catalytic snRNA U6.
Termination of pre-mRNA splicing requires that the ATPase and RNA unwindase Prp43p acts on the catalytic snRNA U6. Genes Dev. 2019 11 01; 33(21-22):1555-1574.
PMID: 31558568

Structure of the DEAH/RHA ATPase Prp43p bound to RNA implicates a pair of hairpins and motif Va in translocation along RNA.
Structure of the DEAH/RHA ATPase Prp43p bound to RNA implicates a pair of hairpins and motif Va in translocation along RNA. RNA. 2017 07; 23(7):1110-1124.
PMID: 28416566

Specific Recognition of a Single-Stranded RNA Sequence by a Synthetic Antibody Fragment.
Specific Recognition of a Single-Stranded RNA Sequence by a Synthetic Antibody Fragment. J Mol Biol. 2016 10 09; 428(20):4100-4114.
PMID: 27593161

The Evolutionarily-conserved Polyadenosine RNA Binding Protein, Nab2, Cooperates with Splicing Machinery to Regulate the Fate of pre-mRNA.
The Evolutionarily-conserved Polyadenosine RNA Binding Protein, Nab2, Cooperates with Splicing Machinery to Regulate the Fate of pre-mRNA. Mol Cell Biol. 2016 11; 36(21):2697-2714.
PMID: 27528618

Reverse transcriptases lend a hand in splicing catalysis.
Reverse transcriptases lend a hand in splicing catalysis. Nat Struct Mol Biol. 2016 06 07; 23(6):507-9.
PMID: 27273636

Cancer therapies activate RIG-I-like receptor pathway through endogenous non-coding RNAs.
Cancer therapies activate RIG-I-like receptor pathway through endogenous non-coding RNAs. Oncotarget. 2016 May 03; 7(18):26496-515.
PMID: 27034163

Spliceosomal DEAH-Box ATPases Remodel Pre-mRNA to Activate Alternative Splice Sites.
Spliceosomal DEAH-Box ATPases Remodel Pre-mRNA to Activate Alternative Splice Sites. Cell. 2016 Feb 25; 164(5):985-98.
PMID: 26919433

View All Publications

Fellow
American Association for the Advancement of Science
2016

Distinguished Investigator Award, Biological Sciences Division
The University of Chicago
2014

Stephen F. Sener, M.D. - Research Scholar Award
American Cancer Society
2006 - 2008

David & Lucile Packard Fellowship in Science and Engineering
Packard Foundation
2001 - 2006

Young Investigator Award
Cancer Research Foundation
2000 - 2001