I’m excited to share our latest study led by
@GiuliaPasquesi out today in @CellPressNews , uncovering a new way transposons have been repurposed for human interferon signaling! Read on for a thread on cryptic splice variants, decoy receptors, and viruses (1/N) 👇🧵
Amazing lab retreat 😉. I LOVE the TE community and everyone I've met through #CSHLTE24. Thanks to everyone for all the knowledge/brainstorming/collaborative advice ❤️ 🥰
Human telomerase threatens genome integrity by adding telomeres to broken chromosomes and is held in check by ATR kinase signaling.
Learn more in Science ⬇️
📄: https://t.co/OgPfniWBsZ
#SciencePerspective: https://t.co/fBAljiyebU
How did we lose our tail? A simple question.. but it wasn't really asked before! We discovered a plausible scenario for the genetic mechanism that led to tail loss. Amazing that such a big change may have been caused by such a small genetic event. https://t.co/0ZR8aH23PJ @BoXia7
🧬 Amazing follow-up on the Arc gene story! Knowing Arc is derived from a retrotransposon, retaining the gag function to create VLPs for intercellular communication. But what regulates the capsid release? And the role of Arc extracellular vesicle? Check it out #ArcGene#VLP#GAG
New preprint 🚨 from the lab! Another paper years in the making from @AliciaRavens and Kaelan Sullivan (not on twitter). TDLR: we describe a new form of intercellular synaptic plasticity! It involves Arc and another cool protein IRSp53. 🧵/1 https://t.co/SbaY06nCAk
We all take repeat annotation in the human genome for granted but are we sure it's correct?
In a 🚨new paper 🚨 from the lab, @xunchen85 shows that up to 30% of primate ERVs/LTRs instances are mis-annotated.
#TransposonFest at @cornell is this Friday! 🧬➰🧬
Join us if you’re around to celebrate the darkest corners of the genome! 🎃
Symposium with 🔥 lineup will showcase some of the exciting work on TEs on our campus + guest of honor @SueWessler for McClintock Lecture @4pm💥
Incredible story 🌟 Truncated isoform of IFN receptor by Exonized Alu that highly expressed in many cell types: IFN receptor decoy. Can’t be more excited to learn about it!
Excited to share our latest preprint, led by @GiuliaPasquesi , on transposons and interferon signaling! 👇 for a 🧵 on cryptic splice variants, decoy receptors, and viruses (1/N)
In general, by sequencing both the eccDNAs and genomes of Arabidopsis epigenetic plants we detected a high eccDNA load associated with genome instability. We speculate that the abundance of eccDNA in ddm1 mutant combinations triggers alternative DNA repair pathways to SVs. 6/n
Finally my graduate work gets out after long process! In this study, we employed our lab's Mobilome-seq/eccDNA-seq methodology to delve into eccDNAs originating from transposable elements within epigenetic plant models. #eccDNA#TEs
Unexpectedly, beyond chimeric or truncated TE insertions linked to eccDNA we found large SVs in hypomethylated plants. We detected large tandem duplications (〜55kb) and small deletions in single plants of ddm1 and ddm1/polIV, complexifying the landscape of genomic variation. 5/n