作者
Leah M. Williams,Melissa M. Inge,Katelyn M. Mansfield,Anna Rasmussen,Jamie Afghani,Mikhail Agrba,Colleen Albert,Cecilia Andersson,Milad Babaei,Mohammad Babaei,Abigail Bagdasaryants,Arianna M. Bonilla,Amanda Browne,Sheldon Carpenter,Tiffany Chen,Blake Christie,Andrew M. Cyr,Katie Dam,Nicholas Dulock,Galbadrakh Erdene,Lindsie Esau,Stephanie Esonwune,Anvita Hanchate,Xin‐Li Huang,Timothy A. Jennings,Aarti Kasabwala,Leanne Kehoe,Ryan Kobayashi,Mi-Gi Lee,Andre LeVan,Yuekun Liu,Emily K. Murphy,Avanti Nambiar,Meagan E. Olive,Devansh Patel,Flaminio Pavesi,Christopher A. Petty,Yelena Samofalova,Selma Sanchez,Camilla Stejskal,Yinian Tang,Alia Yapo,John P. Cleary,Sarah A. Yunes,Trevor Siggers,Thomas D. Gilmore
摘要
Herein, we characterize transcription factor NF-κB from the demosponge Amphimedon queenslandica (Aq). Aq-NF-κB is most similar to NF-κB p100/p105 among vertebrate proteins, with an N-terminal DNA-binding domain, a C-terminal Ankyrin (ANK) repeat domain, and a DNA binding-site profile akin to human NF-κB proteins. Like mammalian NF-κB p100, C-terminal truncation allows nuclear translocation of Aq-NF-κB and increases its transcriptional activation activity. Expression of IκB kinases (IKKs) induces proteasome-dependent C-terminal processing of Aq-NF-κB in human cells, and processing requires C-terminal serines in Aq-NF-κB. Unlike NF-κB p100, C-terminal sequences of Aq-NF-κB do not inhibit its DNA-binding activity. Tissue of a black encrusting demosponge contains NF-κB site DNA-binding activity, as well as nuclear and processed NF-κB. Treatment of sponge tissue with LPS increases both DNA-binding activity and processing of NF-κB. A. queenslandica transcriptomes contain homologs to upstream NF-κB pathway components. This is first functional characterization of NF-κB in sponge, the most basal multicellular animal.