G
Ganesh Shankarling
Researcher at University of Pennsylvania
Publications - 9
Citations - 353
Ganesh Shankarling is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: Alternative splicing & Gene. The author has an hindex of 9, co-authored 9 publications receiving 313 citations. Previous affiliations of Ganesh Shankarling include Texas Tech University Health Sciences Center.
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Journal ArticleDOI
Stem-Loop Recognition by DDX17 Facilitates miRNA Processing and Antiviral Defense
Ryan H. Moy,Brian S. Cole,Ari Yasunaga,Beth Gold,Ganesh Shankarling,Andrew Varble,Jerome M. Molleston,Benjamin R. tenOever,Kristen W. Lynch,Sara Cherry +9 more
TL;DR: DDX17 has dual roles in the recognition of stem loops: in the nucleus for endogenous microRNA (miRNA) biogenesis and in the cytoplasm for surveillance against structured non-self-elements.
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HnRNP L and HnRNP A1 Induce Extended U1 snRNA Interactions with an Exon to Repress Spliceosome Assembly
TL;DR: hnRNP L represses CD45 exon 4 by recruiting hnRNP A1 to a sequence upstream of the 5' splice site and this work demonstrates that conformational perturbations within the spliceosome are a naturally occurring and generalizable mechanism for controlling alternative splicing decisions.
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Transcriptome-Wide RNA Interaction Profiling Reveals Physical and Functional Targets of hnRNP L in Human T Cells
TL;DR: This study uses cross-linking and immunoprecipitation followed by high-throughput sequencing to identify the RNA binding sites of hnRNP L within the transcriptomes of human CD4+ and cultured Jurkat T cells and finds that hn RNP L binds preferentially to transcripts encoding proteins involved in RNA processing and in Wnt and T cell receptor (TCR) signaling.
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Position-dependent activity of CELF2 in the regulation of splicing and implications for signal-responsive regulation in T cells
Sandya Ajith,Matthew R. Gazzara,Brian S. Cole,Ganesh Shankarling,Nicole M. Martinez,Michael J. Mallory,Kristen W. Lynch +6 more
TL;DR: It is proposed that the location of CELF2 binding around an exon is a primary predictor of Celf2 function in a broad range of cellular contexts and is sufficient to explain the bi-directional activity of CELF2 on 2 T cell targets recently reported.
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A family of splice variants of CstF-64 expressed in vertebrate nervous systems.
TL;DR: This is the first report of a family of splice variants encoding a key polyadenylation protein that is expressed in a nervous system-specific manner and it is proposed that βCstF-64 contributes to proteomic diversity by regulating alternative polyadenYLation of neural mRNAs.