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Jesse R. Zamudio

Researcher at University of California, Los Angeles

Publications -  24
Citations -  1872

Jesse R. Zamudio is an academic researcher from University of California, Los Angeles. The author has contributed to research in topics: RNA & Messenger RNA. The author has an hindex of 14, co-authored 21 publications receiving 1574 citations. Previous affiliations of Jesse R. Zamudio include University of California & Massachusetts Institute of Technology.

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LincRNA-p21 Activates p21 In cis to Promote Polycomb Target Gene Expression and to Enforce the G1/S Checkpoint

TL;DR: In this paper, the p53-regulated long noncoding RNA lincRNA-p21 has been shown to act in trans via several mechanisms ranging from repressing genes in the P53 transcriptional network to regulating mRNA translation and protein stability.
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Endogenous miRNA and Target Concentrations Determine Susceptibility to Potential ceRNA Competition

TL;DR: Quantification of cellular miRNA and mRNA/ncRNA target pool levels indicates that miRNA:target pool ratios and an affinity partitioned target pool accurately predict in vivo Ago binding profiles and miRNA susceptibility to target competition.

LincRNA-p21 Activates p21 In cis to Promote Polycomb Target Gene Expression and to Enforce the G1/S Checkpoint

TL;DR: Findings indicate that lincRNA-p21 affects global gene expression and influences the p53 tumor suppressor pathway by acting in cis as a locus-restricted coactivator for p53-mediated p21 expression.
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Antisense RNA polymerase II divergent transcripts are P-TEFb dependent and substrates for the RNA exosome

TL;DR: Data show divergent polymerases are regulated after P-TEFb recruitment with uaRNA levels controlled by the exosome, and Isg20l1 induction reveals equivalent increases in transcriptional activity in sense and antisense directions.
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2′-O-ribose methylation of cap2 in human: function and evolution in a horizontally mobile family

TL;DR: The validation of a human enzyme that methylates the ribose of the second transcribed nucleotide encoded by FTSJD1 is reported, henceforth renamed HMTR2 to reflect function.