David Bartel
Massachusetts Institute of Technology · Biology
Active 1981–2026
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About
David Bartel is a professor of biology at MIT and a core member of the Whitehead Institute. He is an investigator at the Howard Hughes Medical Institute. His research focuses on molecular pathways that regulate eukaryotic gene expression by affecting the stability or translation of mRNAs. Specifically, he studies microRNAs and other small RNAs that specify the destruction and/or translational repression of mRNAs. His work also involves studying mRNAs, with particular attention to their untranslated regions and poly(A) tails, and how these regions recruit and mediate regulatory phenomena. Dr. Bartel has made significant contributions to understanding the biochemical basis of microRNA targeting efficacy, the coupling between poly(A)-tail length and translational efficiency, and the mechanisms of target-directed microRNA degradation. His research has advanced knowledge of noncoding regulatory RNAs, their role in gene regulation, and their impact on cellular processes.
Research topics
- Biology
- Biochemistry
- Cell biology
Selected publications
The ZSWIM8 ubiquitin ligase mediates target-directed microRNA degradation
Science · 2020-11-12 · 247 citations
articleOpen accessSenior authorCorrespondingMicroRNAs (miRNAs) associate with Argonaute (AGO) proteins to direct widespread posttranscriptional gene repression. Although association with AGO typically protects miRNAs from nucleases, extensive pairing to some unusual target RNAs can trigger miRNA degradation. We found that this target-directed miRNA degradation (TDMD) required the ZSWIM8 Cullin-RING E3 ubiquitin ligase. This and other findings support a mechanistic model of TDMD in which target-directed proteolysis of AGO by the ubiquitin-…
Cell · 2022 · 162 citations
Genome Research · 2023-08-02 · 32 citations
articleOpen accessSenior authorMicroRNAs (miRNAs) pair to sites in mRNAs to direct the degradation of these RNA transcripts. Conversely, certain RNA transcripts can direct the degradation of particular miRNAs. This target-directed miRNA degradation (TDMD) requires the ZSWIM8 E3 ubiquitin ligase. Here, we report the function of ZSWIM8 in the mouse embryo. Zswim8 −/− embryos were smaller than their littermates and died near the time of birth. This highly penetrant perinatal lethality was apparently caused by a lung sacculation…
Nuclear release of eIF1 restricts start-codon selection during mitosis
Nature · 2024-10-23 · 29 citations
articleOpen accessControl of poly(A)-tail length and translation in vertebrate oocytes and early embryos
Developmental Cell · 2024-03-08 · 29 citations
articleOpen accessSenior authorCorrespondingDuring oocyte maturation and early embryogenesis, changes in mRNA poly(A)-tail lengths strongly influence translation, but how these tail-length changes are orchestrated has been unclear. Here, we performed tail-length and translational profiling of mRNA reporter libraries (each with millions of 3' UTR sequence variants) in frog oocytes and embryos and in fish embryos. Contrasting to previously proposed cytoplasmic polyadenylation elements (CPEs), we found that a shorter element, UUUUA, together…
Recent grants
Post-transcriptional gene regulation
NIH · $7.0M · 2016–2026
NIH · $7.3M · 2016
NIH · $230k · 2011
Frequent coauthors
- 94 shared
Stephen W. Eichhorn
Harvard University
- 88 shared
Alexander O. Subtelny
Harvard University
- 85 shared
Sean E. McGeary
Center for Systems Biology
- 69 shared
Vikram Agarwal
University of Washington
- 66 shared
Wendy K. Johnston
Howard Hughes Medical Institute
- 65 shared
David E. Weinberg
University of California, San Francisco
- 64 shared
Nelson C. Lau
Boston University
- 58 shared
Charlie Y. Shi
Whitehead Institute for Biomedical Research
Labs
David Bartel LabPI
Education
- 1993
Ph.D., Virology
Harvard University
- 1982
B.A., Biology
Goshen College
Awards & honors
- Member, National Academy of Sciences (2011)
- HHMI Investigator (2005)
- National Academy of Sciences Award in Molecular Biology (200…
- AAAS Newcomb Cleveland Prize (2002)
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