Image_1_Ancient Origin of the CARD–Coiled Coil/Bcl10/MALT1-Like Paracaspase Signaling Complex Indicates Unknown Critical Functions.PDF

التفاصيل البيبلوغرافية
العنوان: Image_1_Ancient Origin of the CARD–Coiled Coil/Bcl10/MALT1-Like Paracaspase Signaling Complex Indicates Unknown Critical Functions.PDF
المؤلفون: Jens Staal, Yasmine Driege, Mira Haegman, Alice Borghi, Paco Hulpiau, Laurens Lievens, Ismail Sahin Gul, Srividhya Sundararaman, Amanda Gonçalves, Ineke Dhondt, Jorge H. Pinzón, Bart P. Braeckman, Ulrich Technau, Yvan Saeys, Frans van Roy, Rudi Beyaert
سنة النشر: 2018
المجموعة: Frontiers: Figshare
مصطلحات موضوعية: Immunology, Applied Immunology (incl. Antibody Engineering, Xenotransplantation and T-cell Therapies), Autoimmunity, Cellular Immunology, Humoural Immunology and Immunochemistry, Immunogenetics (incl. Genetic Immunology), Innate Immunity, Transplantation Immunology, Tumour Immunology, Immunology not elsewhere classified, Genetic Immunology, Animal Immunology, Veterinary Immunology, signal transduction, molecular evolution, protein–protein interaction, structure–function analysis, NF-kappaB, coral bleaching, Nematostella vectensis, Caenorhabditis elegans
الوصف: The CARD–coiled coil (CC)/Bcl10/MALT1-like paracaspase (CBM) signaling complexes composed of a CARD–CC family member (CARD-9, -10, -11, or -14), Bcl10, and the type 1 paracaspase MALT1 (PCASP1) play a pivotal role in immunity, inflammation, and cancer. Targeting MALT1 proteolytic activity is of potential therapeutic interest. However, little is known about the evolutionary origin and the original functions of the CBM complex. Type 1 paracaspases originated before the last common ancestor of planulozoa (bilaterians and cnidarians). Notably in bilaterians, Ecdysozoa (e.g., nematodes and insects) lacks Bcl10, whereas other lineages have a Bcl10 homolog. A survey of invertebrate CARD–CC homologs revealed such homologs only in species with Bcl10, indicating an ancient common origin of the entire CBM complex. Furthermore, vertebrate-like Syk/Zap70 tyrosine kinase homologs with the ITAM-binding SH2 domain were only found in invertebrate organisms with CARD–CC/Bcl10, indicating that this pathway might be related to the original function of the CBM complex. Moreover, the type 1 paracaspase sequences from invertebrate organisms that have CARD–CC/Bcl10 are more similar to vertebrate paracaspases. Functional analysis of protein–protein interactions, NF-κB signaling, and CYLD cleavage for selected invertebrate type 1 paracaspase and Bcl10 homologs supports this scenario and indicates an ancient origin of the CARD–CC/Bcl10/paracaspase signaling complex. By contrast, many of the known MALT1-associated activities evolved fairly recently, indicating that unknown functions are at the basis of the protein conservation. As a proof-of-concept, we provide initial evidence for a CBM- and NF-κB-independent neuronal function of the Caenorhabditis elegans type 1 paracaspase malt-1. In conclusion, this study shows how evolutionary insights may point at alternative functions of MALT1.
نوع الوثيقة: still image
اللغة: unknown
العلاقة: https://figshare.com/articles/figure/Image_1_Ancient_Origin_of_the_CARD_Coiled_Coil_Bcl10_MALT1-Like_Paracaspase_Signaling_Complex_Indicates_Unknown_Critical_Functions_PDF/6342896Test
DOI: 10.3389/fimmu.2018.01136.s002
الإتاحة: https://doi.org/10.3389/fimmu.2018.01136.s002Test
https://figshare.com/articles/figure/Image_1_Ancient_Origin_of_the_CARD_Coiled_Coil_Bcl10_MALT1-Like_Paracaspase_Signaling_Complex_Indicates_Unknown_Critical_Functions_PDF/6342896Test
حقوق: CC BY 4.0
رقم الانضمام: edsbas.2659D26C
قاعدة البيانات: BASE