Xun Chen (@xunchen85) header
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Shanghai Institute of Immunity and Infection (Former Institut Pasteur of Shanghai), CAS

Shanghai, China
Joined April 2015
Photo by Xun Chen (@xunchen85)Photo by Xun Chen (@xunchen85)Photo by Xun Chen (@xunchen85)Photo by Xun Chen (@xunchen85)Photo by Xun Chen (@xunchen85)Photo by Xun Chen (@xunchen85)Photo by Xun Chen (@xunchen85)
Super excited to share our latest #preprint on the TE classification/annotation and regulatory evolution from our lab @guilbourque at @Ashbi_KyotoU. Check it out here! 🧵 Cryptic endogenous retrovirus subfamilies in the primate lineage doi.org/10.1101/2023.12.07.5…
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Xun Chen retweeted
Why don't humans have tails? A genetics study finds that a mobile genetic sequence inserted into a gene for tail development contributed to tail loss as early apes evolved. go.nature.com/3Te8t4C
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Our paper on the ancestral genome-assisted TE annotation method/resource is out in @CellGenomics! Enhanced annotation is now available for multiple species, including human and mouse, with ~70% increase in ancient TEs. cell.com/cell-genomics/fullt…
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I've gotten several requests recently for permission to use the notes from my computational biology class: github.com/pachterlab/BI-BE-… A reminder that they're licensed under CC BY 4.0: you're free to share and adapt, just give appropriate credit and indicate if changes were made.
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[News release] ASHBi researchers identify and selectively manipulate the neural circuits underlying the balance of risk vs. reward decision-making using optogenetics in primates. ➡️Article science.org/doi/10.1126/scie… ➡️Press Release ashbi.kyoto-u.ac.jp/news/202… @ScienceMagazine
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Check out our latest review | LINE-1 retrotransposition and its deregulation in cancers: implications for therapeutic opportunities by @CarlosMendezPhD. Our thanks to @GenesDev. genesdev.cshlp.org/content/e…
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“Transposable elements contribute to nearly 80% of human-specific candidate cis-regulatory elements in cortical cells” 🧠 …🤯 literally! Amazing dataset 🔥 Congrats to all involved! nature.com/articles/s41586-0…
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Very happy to share our new paper on how SOX2 instructs pluripotency program transition in vivo in mouse E3.5-E7.5 embryos. Spearheaded by our super team: Lijia Li, Fangnong Lai, Xiaoyu Hu and Bofeng Liu. Wonderful collaboration with Amy Ralston. (1/n) science.org/doi/10.1126/scie…
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💥 New preprint! Really excited about this work brilliantly led by Manu @manvendr7 & Sabrina Leddy in collab with @TheNixonLab - check it out and let us know what you think!
🎈🎆Beyond thrilled to drop new preprint exploring how #transposons (TEs) contribute to natural resistance to HIV in “Elite Controllers” (ECs) biorxiv.org/content/10.1101/… a work from @TheNixonLab and @CedricFeschotte Lab Please see 🧵till end, it gets better with each 🧵 1/12
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We found a high epigenetic heterogeneity per subfamily which was well rearranged by the rooted tree and phyletic groups. And the reconstituted MER11 phyletic groups display a more consistent epigenetic profile compared to the original subfamily annotations.
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Focusing on the youngest phyletic group “MER11_G4”, we revealed the gain of SOX-related motif in this phyletic group was due to a single-nucleotide deletion and occurred in humans and chimpanzees but not in macaques. It also significantly increased their regulatory potential.
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In the end, we applied the approach to other simian-specific LTR subfamilies. Among 53 subfamilies analyzed, we corrected 30% instances from 26 subfamilies. We found that the phyletic groups we characterized were enriched for different epigenetic marks TFs and KRAB-ZNFs.
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We then developed a new annotation approach based on phylogenetic analysis and cross-species conservation to correct it. Focusing on MER11 subfamilies, we reassigned instances from the three subfamilies (MER11A/B/C) into four groups, we defined as “phyletic groups”.
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