Pregled bibliografske jedinice broj: 560023
SHARPIN forms a linear ubiquitin ligase complex regulating NF-κB activity and apoptosis
SHARPIN forms a linear ubiquitin ligase complex regulating NF-κB activity and apoptosis // Nature, 471 (2011), 7340; 637-641 (međunarodna recenzija, pismo, znanstveni)
CROSBI ID: 560023 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
SHARPIN forms a linear ubiquitin ligase complex regulating NF-κB activity and apoptosis
Autori
Ikeda, Fumiyo ; Lissanu Deribe, Yonathan ; Skånland, Sigrid S. ; Stieglitz, Benjamin ; Grabbe, Caroline ; Franz-Wachtel, Mirita ; van Wijk, Sjoerd J. L. ; Goswami, Panchali ; Nagy, Vanja ; Terzić, Janoš ; Tokunaga, Fuminori ; Androulidaki, Ariadne ; Nakagawa, Tomoko ; Pasparakis, Manolis ; Iwai, Kazuhiro ; Sundberg, John P. ; Schaefer, Liliana ; Rittinger, Katrin ; Maček, Boris ; Đikić, Ivan
Izvornik
Nature (0028-0836) 471
(2011), 7340;
637-641
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, pismo, znanstveni
Ključne riječi
polyubiquitin chains; immune-system; proteins; activation; fractionation; dermatitis; proteomics; induction; nemo
Sažetak
SHARPIN is a ubiquitin-binding and ubiquitin-like-domain-containing protein which, when mutated in mice, results in immune system disorders and multi-organ inflammation. Here we report that SHARPIN functions as a novel component of the linear ubiquitin chain assembly complex (LUBAC) and that the absence of SHARPIN causes dysregulation of NF-κB and apoptotic signalling pathways, explaining the severe phenotypes displayed by chronic proliferative dermatitis (cpdm) in SHARPIN-deficient mice. Upon binding to the LUBAC subunit HOIP (also known as RNF31), SHARPIN stimulates the formation of linear ubiquitin chains in vitro and in vivo. Coexpression of SHARPIN and HOIP promotes linear ubiquitination of NEMO (also known as IKBKG), an adaptor of the IκB kinases (IKKs) and subsequent activation of NF-κB signalling, whereas SHARPIN deficiency in mice causes an impaired activation of the IKK complex and NF-κB in B cells, macrophages and mouse embryonic fibroblasts (MEFs). This effect is further enhanced upon concurrent downregulation of HOIL-1L (also known as RBCK1), another HOIP-binding component of LUBAC. In addition, SHARPIN deficiency leads to rapid cell death upon tumour-necrosis factor α (TNF-α) stimulation via FADD- and caspase-8-dependent pathways. SHARPIN thus activates NF-κB and inhibits apoptosis via distinct pathways in vivo.
Izvorni jezik
Engleski
POVEZANOST RADA
Projekti:
216-0000000-3348 - ULOGA UPALNIH PROCESA U NASTANKU MALIGNIH TUMORA (Terzić, Janoš, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Split
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- MEDLINE