@JoePetersLab

Professor and Chair, Dept Microbiology Cornell Ithaca. Interested in genome evolution and mobile DNA, especially Tn7 and CRISPR-Cas transposition systems

Ithaca, NY
Joined October 2017
It was a pleasure working with @PopoMicro on this review of CRISPR-Cas associated transposons (CAST). Hopefully it gives a sense for the diversity of Tn7-like transposons and CRISPR systems that independently combined.go.shr.lc/444PwFh
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The Peters lab is looking for a new team member! The role transposons play in evolution, basic mechanisms regulating transposition, and applying transposons as tools for genome modification with a special focus on guide RNA-directed transposition cornell.wd1.myworkdayjobs.co…
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In addition to a highly collaborative lab environment we interact with a dynamic Microbiology community, DNA Replication, Recombination and Repair group and a growing list of transposon-centered lab cals.cornell.edu/microbiolog… cals.cornell.edu/microbiolog…
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Functional RNA splitting drove the evolutionary emergence of type V CR... sciencedirect.com/science/ar…
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Here is a link to a new preprint from the lab, a collaborative effort between our lab and Michelle Wang's lab here at Cornell. biorxiv.org/cgi/content/shor…
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Tn7 family transposons that include all guide RNA-directed transposons (CAST) are common in bacteria. We now find diverse representatives across archaea, many in the Asgard group. Reviving an Asgard element confirmed the exciting behaviors of the family biorxiv.org/content/10.1101/…
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Joseph E. Peters retweeted
Replying to @JoePetersLab
Very cool story lead by @JoePetersLab reveals another level of how transposons battle with their hosts. Grateful to have had a chance to participate with Popo @PopoMicro, Joe and the team!
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Joseph E. Peters retweeted
Transposons, or “jumping genes” – DNA segments that can move from one part of the genome to another – are key to bacterial evolution and the development of antibiotic resistance. Cornell researchers have discovered a new mechanism these genes use to survive and propagate in bacteria with linear DNA, with applications in biotechnology and drug development. “This is a big part of their biology,” said senior author Joseph Peters, professor of microbiology in @CornellCALS. “Bacteria are like these little tinkerers. They’re always collecting these mobile DNA pieces, and they’re making new functions all the time – everything in antibiotic resistance is really about mobile genetic elements and almost always transposons that can move between bacteria.” With some technologies not available even five years ago, the researchers identified several families of transposons in cyanobacteria and Streptomyces that, using different mechanisms, can find and insert themselves at the telomere, with benefits for the transposon and their bacterial host. For one, inserting at the end of the chromosome helps the transposon avoid genes for the cell’s core functioning, which reside in the middle of the chromosomes; transposons that can target the ends are less likely to disrupt an essential function or cause cell death. More at news.cornell.edu/stories/202….
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🧬 Thrilled to share our latest research on Retrons—a new chapter in this fascinating field! 🌟In this @MolecularCell paper, we reveal how Retron-Eco1 defends against phages. bit.ly/3WOlbsY Check the 🧵below! (1/20)
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Joseph E. Peters retweeted
#CRISPR revolutionized medicine, but where did its RNA-guided mechanisms come from? Using #AI, we unearthed new Cas13s and found they evolved from toxin-antitoxins, revealing how nature created these amazing reprogrammable molecules. Discover the recipe: doi.org/10.1016/j.cell.2025.…
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Very excited about this work from graduate student Laura Chacon Machado now published in Mobile DNA, “A family of Tn7-like transposons evolved to target CRISPR repeats”!
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📢 Prof. Marcin Nowotny has received the Prime Minister’s Award! The prize honors his research on protein-nucleic acid interactions, advancing our understanding of cellular information decoding. 👉 Read more: tinyurl.com/MNowotnyPMAward
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