The kinase DYRK1A can aid #coronavirus entry by driving #chromatin accessibility & active transcription at coronavirus receptor gene loci, independent of its catalytic function #SARSCoV2 #SARSCoV #MERSCoV @madisonstrine &co @WilenLab #PLOSBiology https://t.co/5CaR7ndoC9 https://t.co/3IdoGi5GFj
DYRK1A promotes viral entry of highly pathogenic human coronaviruses in a kinase-independent manner.
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Jun 2023 – Aug 2024Where it's discussed
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What people are saying
The collected discussions clearly show enthusiasm for the discovery that DYRK1A influences coronavirus entry through epigenetic mechanisms, with phrases like 'new drug target' and 'important insight' underscoring the perceived importance and potential impact of this research, while scientific detail and references to mechanisms reflect active and engaged analysis.
Most discussions are highly supportive, emphasizing the importance of DYRK1A in viral entry and potential therapeutic implications.
The discussions demonstrate strong interest, highlighting detailed mechanisms and future research directions.
The posts show active engagement with mentions of molecular mechanisms, gene regulation, and potential drug targets, indicating a deep understanding of the research.
Many posts suggest that the findings could significantly influence coronavirus treatment strategies and epigenetic research, indicating high perceived impact.
Abstract in brief
- DYRK1A enhances the entry of dangerous human coronaviruses like SARS-CoV, SARS-CoV-2, and MERS-CoV by increasing the expression of the receptors ACE2 and DPP4, and this process does not depend on its kinase activity.
- The protein promotes gene transcription by making DNA more accessible at the ACE2 gene’s promoter and an enhancer region, aiding the virus's ability to infect cells.
- This function of DYRK1A is conserved across different species, including humans and non-human primates, making it a potential target for therapies to prevent coronavirus infections.
Top posts
Most liked on X and BlueskyThe kinase DYRK1A can aid #coronavirus entry by driving #chromatin accessibility & active transcription at coronavirus receptor gene loci, independent of its catalytic function #SARSCoV2 #SARSCoV #MERSCoV @madisonstrine &co @WilenLab #PLOSBiology https://t.co/5CaR7ncQMB https://t.co/I6kphZ7q9K
Key regulator of COVID viral receptor may be new drug target @plos https://t.co/3EWOy37juU https://t.co/jJU4wOaI5k
The kinase DYRK1A can aid #coronavirus entry by driving #chromatin accessibility & active transcription at coronavirus receptor gene loci, independent of its catalytic function #SARSCoV2 #SARSCoV #MERSCoV @madisonstrine &co @WilenLab #PLOSBiology https://t.co/5CaR7ndoC9 https://t.co/MxKAoi6ceM
Fantastic new paper from @WilenLab and @madisonstrine. Congrats to everyone. DYRK1A promotes viral entry of highly pathogenic human coronaviruses in a kinase-independent manner | PLOS Biology https://t.co/kYKhxsoiZi
From @PLOSBiology - DYRK1A promotes viral entry of highly pathogenic human coronaviruses in a kinase-independent manner https://t.co/HCxMVMPYtK #bwfcams https://t.co/r9B3zt9Nt5
All mentions
DYRK1A's Role in Enhancing Coronavirus Cell Entry Despite Kinase Independence
DYRK1A promotes entry of highly pathogenic human coronaviruses by increasing ACE2 and DPP4 receptor expression, independent of its kinase activity. This conserved process across species highlights DYRK1A as a potential…
DYRK1A promotes viral entry of highly pathogenic human coronaviruses in a kinase-independent manner https://t.co/1Cj6svdz2M
In summary, we report that DYRK1A is a novel regulator of ACE2 and DPP4 expression that may dictate susceptibility to multiple highly pathogenic human coronaviruses. https://t.co/WJJXSpBv8F
Part 121. DYRK1A promotes DNA accessibility at the ACE2 promoter and a putative distal enhancer, facilitating transcription and gene expression. #DYRK1A promotes #viralentry of highly pathogenic human coronaviruses in a kinase-independent manner https://t.co/PFP1LnoJ6O https://t.co/gxUxCe1V1n
This along with our companion papers provides important insight into the epigenetic regulation of ACE2. If and how cBAF, Dyrk1a, and Kdm6a/Kmt2d interact to regulate ACE2 is an open question. https://t.co/yolEM6Yugc https://t.co/iySOqzs5EC
RT @medical_xpress: Key regulator of COVID viral receptor may be new drug target @plos https://t.co/3EWOy37juU https://t.co/jJU4wOaI5k
RT @PLOSBiology: The kinase DYRK1A can aid #coronavirus entry by driving #chromatin accessibility & active transcription at coronavirus rec…
The kinase DYRK1A can aid #coronavirus entry by driving #chromatin accessibility & active transcription at coronavirus receptor gene loci, independent of its catalytic function #SARSCoV2 #SARSCoV #MERSCoV @madisonstrine &co @WilenLab #PLOSBiology https://t.co/5CaR7ndoC9 https://t.co/MxKAoi6ceM
RT @PLOSBiology: The kinase DYRK1A can aid #coronavirus entry by driving #chromatin accessibility & active transcription at coronavirus rec…
RT @PLOSBiology: The kinase DYRK1A can aid #coronavirus entry by driving #chromatin accessibility & active transcription at coronavirus rec…
RT @BWFUND: From @PLOSBiology - DYRK1A promotes viral entry of highly pathogenic human coronaviruses in a kinase-independent manner https:/…
From @PLOSBiology - DYRK1A promotes viral entry of highly pathogenic human coronaviruses in a kinase-independent manner https://t.co/HCxMVMPYtK #bwfcams https://t.co/r9B3zt9Nt5
The kinase DYRK1A can aid #coronavirus entry by driving #chromatin accessibility & active transcription at coronavirus receptor gene loci, independent of its catalytic function #SARSCoV2 #SARSCoV #MERSCoV @madisonstrine &co @WilenLab #PLOSBiology https://t.co/5CaR7ncQMB https://t.co/I6kphZ7q9K
RT @PLOSBiology: The kinase DYRK1A can aid #coronavirus entry by driving #chromatin accessibility & active transcription at coronavirus rec…
Fantastic new paper from @WilenLab and @madisonstrine. Congrats to everyone. DYRK1A promotes viral entry of highly pathogenic human coronaviruses in a kinase-independent manner | PLOS Biology https://t.co/kYKhxsoiZi
RT @PLOSBiology: The kinase DYRK1A can aid #coronavirus entry by driving #chromatin accessibility & active transcription at coronavirus rec…
The kinase DYRK1A can aid #coronavirus entry by driving #chromatin accessibility & active transcription at coronavirus receptor gene loci, independent of its catalytic function #SARSCoV2 #SARSCoV #MERSCoV @madisonstrine &co @WilenLab #PLOSBiology https://t.co/5CaR7ndoC9 https://t.co/3IdoGi5GFj
#PLOSBiology: DYRK1A promotes viral entry of highly pathogenic human coronaviruses in a kinase-independent ma ... https://t.co/2EvlsMZ9nl
DYRK1A promotes viral entry of highly pathogenic human coronaviruses in a kinase-independent manner https://t.co/BPGgF4gjYE
RT @medical_xpress: Key regulator of COVID viral receptor may be new drug target @plos https://t.co/3EWOy37juU https://t.co/jJU4wOaI5k
RT @medical_xpress: Key regulator of COVID viral receptor may be new drug target @plos https://t.co/3EWOy37juU https://t.co/jJU4wOaI5k
RT @medical_xpress: Key regulator of COVID viral receptor may be new drug target @plos https://t.co/3EWOy37juU https://t.co/jJU4wOaI5k
RT @medical_xpress: Key regulator of COVID viral receptor may be new drug target @plos https://t.co/3EWOy37juU https://t.co/jJU4wOaI5k
RT @medical_xpress: Key regulator of COVID viral receptor may be new drug target @plos https://t.co/3EWOy37juU https://t.co/jJU4wOaI5k
Key regulator of COVID viral receptor may be new drug target @plos https://t.co/3EWOy37juU https://t.co/jJU4wOaI5k