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Noga Sharlin

@nogasharlin.bsky.social
57 followers 110 following 2 posts

PhD student at the University of Calgary Studying human coronaviruses and innate immune responses in the Corcoran Lab

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Reposted by Noga Sharlin
Mariel Kleer @marielkleer.bsky.social · 17/09/2026
So happy to have this story out! What started as a project about the protein products of a polycistronic mRNA ended up becoming a story about how RNA-mediated assembly of nuclear speckles promotes viral gene expression. What a ride, some very good days on the microscope!! 🔬 @corcoranlab.bsky.social
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Reposted by Noga Sharlin
Cell Reports @cp-cellreports.bsky.social · 05/09/2026
PKR engages viral RNA and intron-retained host transcripts during poxvirus infection
dlvr.it
PKR engages viral RNA and intron-retained host transcripts during poxvirus infection
Zhang et al. show that during poxvirus infection, protein kinase R binds not only viral RNAs but also host intron-retained transcripts that accumulate. Cellular PACT and viral E3 set activation thresholds for PKR, linking RNA processing, viral replication, and innate immunity.
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Reposted by Noga Sharlin
PLOS Biology @plosbiology.org · 18/08/2026
Stress granules help #antiviral defense, but what do they do during RNA #virus infection? Reto Lang, @profvolkerthiel.bsky.social &co show that #coronavirus & #alphavirus infections generate #StressGranules with distinct kinetics, proteomes & viral RNA content @plosbiology.org 🧪 plos.io/4wARYzZ
Proposed model of host-virus interaction in the context of SGs during SFV and MHV infections in cells. Top: SFV seems to induce canonical SGs early in infection characterized by the presence of well-known SG marker proteins like eukaryotic translation initiation factors. The sequestration of especially the eIFs, which are required by the virus for efficient viral translation, as well as the accumulation of SFV genomic RNA in these condensates could have negative effects on viral growth. Thus, the virus dissolves the SGs with progressing infection. Bottom: In contrast, MHV seems to prevent induction of canonical SGs early in infection. Only with the onset of exponential release of new virus particles, accumulations positive for the major SG markers G3BP1, TIA1, and UBAP2L are formed in the cytoplasm. A reduced abundance of many known SG proteins including eIFs compared to canonical SGs suggests a type of atypical SGs. Together with the efficient exclusion of MHV viral RNA, this gives rise to the apparent tolerance of these condensates by MHV later in infection.
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Noga Sharlin @nogasharlin.bsky.social · 17/07/2026
Excited to have this preprint out showing that N proteins of human coronaviruses differ in their ability to inhibit antiviral responses! Many thanks to my supervisor Jennifer Corcoran @corcoranlab.bsky.social, as well as to co-authors @rorymulloy.bsky.social and Madeline Day for all their support!
biorxiv.org
Human coronavirus nucleocapsid proteins have disparate innate immune evasion abilities
During infection, coronaviruses produce abundant double-stranded RNA (dsRNA) which can induce antiviral innate immune responses such as the interferon, 2'-5'-oligoadenylate synthetase (OAS)/RNase L, a...
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Reposted by Noga Sharlin
Fletcher Lab @fletcherlab.bsky.social · 03/06/2026
Delighted to share our article on the functional expansion of OAS2 via alt. splicing. link.springer.com/article/10.1... A tour de force from PhD student Emma Davies and friends.
link.springer.com
Alternative splicing broadens antiviral diversity at the human OAS2 locus - The EMBO Journal
Interferons (IFN) are cytokines that regulate the expression of hundreds of genes during viral infections to generate a broadly antiviral environment in the stimulated cell. Antiviral breadth is provi...
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Craig McCormick @craigmccormick.bsky.social · 13/05/2026
Our study of coronavirus structural proteins that interfere with host responses to infection, led by Drs. Taylor Caddell and Eric Pringle, with support from colleagues @rorymulloy.bksy.social and @corcoranlab.bsky.social, is now published in @PLOSPathogens journals.plos.org/plospathogen... (1/8)
journals.plos.org
Coronavirus M protein disperses the trans-Golgi network and inhibits anterograde protein trafficking in the secretory pathway
Author summary Coronaviruses (CoVs) use the endoplasmic reticulum (ER) for synthesis and processing of viral transmembrane proteins, including those that sculpt ER membranes into replication compartme...
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Rory Mulloy @rorymulloy.bsky.social · 19/04/2026
SUPER COOL to have my recent paper highlighted by CoV transcription legends, Drs Isabel Sola & Sonia Zuñiga in a PLoS Bio Primer. A much better read than the AI summary of the paper 💥 journals.plos.org/plosbiology/...
journals.plos.org
New transcription signals in SARS-CoV-2 reshape virus–host interactions
Non-spike changes driving SARS-CoV-2 fitness remain undiscovered. This Primer comments on two PLOS Biology papers that show that evolutionary N gene mutations create a transcription-regulating sequenc...
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Reposted by Noga Sharlin
Rory Mulloy @rorymulloy.bsky.social · 02/04/2026
💥 Paper published 💥 Curious how #SARS2 has changed since jumping into humans? We were too! journals.plos.org/plosbiology/... 🧵 🧵 🧵
journals.plos.org
Evolution of a truncated nucleocapsid protein enhances SARS-CoV-2 fitness by suppressing antiviral responses
SARS-CoV-2 has evolved to optimize its replication fitness in the human host. This study shows that a nucleocapsid gene mutation enhances production of a truncated protein that boosts viral fitness in...
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Noga Sharlin @nogasharlin.bsky.social · 02/04/2026
So proud to have worked alongside @rorymulloy.bsky.social and @corcoranlab.bsky.social on this amazing project, now out in @plosbiology.org! journals.plos.org/plosbiology/...
journals.plos.org
Evolution of a truncated nucleocapsid protein enhances SARS-CoV-2 fitness by suppressing antiviral responses
SARS-CoV-2 has evolved to optimize its replication fitness in the human host. This study shows that a nucleocapsid gene mutation enhances production of a truncated protein that boosts viral fitness in...
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Reposted by Noga Sharlin
Karim Majzoub @karimaj.bsky.social · 06/03/2026
We found a viral Trojan Horse: a virus can hide inside another virus.This one surprised us: deltaviruses don’t just borrow a helper virus. They can travel inside it. A literal Trojan Horse “virus-in-a-virus” route into cells. 🤯 Kudos to 1st author @viroscope.bsky.social and co-authors !
sciencedirect.com
Deltaviruses spread through a viral Trojan Horse
Hepatitis D-like satellite viruses, known as deltaviruses, have been recently discovered in a wide range of animals. These viruses are thought to expr…
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Reposted by Noga Sharlin
Kranzusch Lab @kranzuschlab.bsky.social · 17/02/2026
Max Fels @mfels.bsky.social from our lab discovers giant DNA viruses that infect amoeba encode eIF4E and the entire suite of 4F complex proteins to control mRNA translation, including beautiful crystal structures of viral 4E bound to modified mRNA 5' caps: www.cell.com/cell/fulltex...
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AJ te Velthuis @ajtevelthuis.bsky.social · 02/01/2026
Congratulations to @karishmabisht.bsky.social with her paper on the effect of fever on influenza replication and innate immune activation! www.science.org/doi/10.1126/...
science.org
Febrile temperature activates the innate immune response by promoting aberrant influenza A virus RNA synthesis
Fever promotes aberrant influenza A virus RNA synthesis and innate immune activation.
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Reposted by Noga Sharlin
Nature Microbiology @natmicrobiol.nature.com · 15/10/2025
The IFIT2–IFIT3 antiviral complex targets short 5’ untranslated regions on viral mRNAs for translation inhibition By Dustin Glasner, Matthew Daugherty & colleagues. #microsky www.nature.com/articles/s41...
nature.com
The IFIT2–IFIT3 antiviral complex targets short 5’ untranslated regions on viral mRNAs for translation inhibition - Nature Microbiology
Viruses generally have compact genomes, resulting in many viral mRNAs with short 5’ untranslated regions. An antiviral complex exploits this feature of viral mRNAs to selectively inhibit viral protein...
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Ryan Hisner @ryanhisner.bsky.social · 26/05/2025
An awesome preprint on the novel, unsung SARS-CoV-2 N* protein came out recently, authored by @corcoranlab.bsky.social and @rorymulloy.bsky.social. I’ve previously written on N*’s demise in XEC, the top variant for several months, but… threadreaderapp.com/thread/18373... 1/34
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Indra_Beķere @indrabekere.bsky.social · 23/05/2025
Our manuscript on dsRNA sensor OAS2 from the lab of @oliveiramann.bsky.social is now out in @cp-molcell.bsky.social ! Thanks again to the whole team for their effort putting this story together!
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Emily Bruce @brucelab.bsky.social · 29/04/2025
Very happy that this story is now published in @plosbiology.org. It includes lots of additional data, (creation of the G215S mutant) & demonstrates the increased growth/ oligomerization of N is specific to the cysteine at 215. Thanks to the coauthors, reviewers and editors who helped improve it!
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Chris Sullivan @sullivanlab.bsky.social · 22/04/2025
Previously, KO and overexpression showed host RNA 5’ triphosphatase DUSP11 can reduce RIG-I sensitivity. Here, we show poxviruses code for viral DUSP11 that can regulate host RNP III transcripts and RIG-I, providing evolutionary support DUSP11 can be pro-viral. journals.plos.org/plospathogen...
journals.plos.org
Viral piracy of host RNA phosphatase DUSP11 by avipoxviruses
Author summary Viruses face a critical challenge of disabling or avoiding host immune defenses. Cells typically recognize the presence of a virus through specific molecular markers, including triphosp...
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Emmanuelle Genoyer @immunuelle.bsky.social · 18/04/2025
Check out this fun preview of my postdoctoral work! It highlights our findings plus lots of intriguing questions that I’m super excited to tackle in the coming years. (And the model is beautiful! Thank you! 🧑‍🎨 )
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Nature @nature.com · 12/03/2025
After 150,000 articles and 17 million genome sequences, what has science taught us about SARS-CoV-2? go.nature.com/4iDKrtw
go.nature.com
Four ways COVID changed virology: lessons from the most sequenced virus of all time
After 150,000 articles and 17 million genome sequences, what has science taught us about SARS-Cov-2?
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Reposted by Noga Sharlin
Corcoran Lab @corcoranlab.bsky.social · 27/02/2025
Our newest work reveals that SARS-CoV-2 evolved to produce a truncated version of its N protein to antagonize antiviral responses. This 'mini' N, called N*M210, sequesters dsRNA, blocks interferon activation, defeats RNaseL & disassembles stress granules and p-bodies. www.biorxiv.org/content/10.1...
biorxiv.org
A truncated SARS-CoV-2 nucleocapsid protein enhances virus fitness by evading antiviral responses
Viruses face a selective pressure to evade cellular antiviral responses to control the outcome of an infection. However, due to their limited genome size, viruses must adopt unique strategies to confr...
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