IndraLab
Statements
reach
"As A20 ZF4 proteins are recruited poorly to TNFR signaling complexes, the presence of normal NF-kappaB signaling in Tnfaip3 OTU and ZF4 cells also raises the interesting possibility that A20 OTU proteins may dimerize with A20 ZF4 proteins and recruit the latter to TNFR signaling complexes in Tnfaip3 OTU and ZF4 cells."
reach
"A20 is regulated at the level of gene transcription 6, whereby NF-kappaB activation induces TNFAIP3 expression XREF_BIBR, XREF_BIBR forming a negative feedback loop, and the inhibitory activities of A20 enzymatic sites are enhanced by IKKB mediated serine phosphorylation at Ser381 XREF_BIBR, XREF_BIBR."
| PMC
reach
"The observation that A20 OTU and A20 ZF4 proteins complement each other to normally regulate NF-kappaB signaling in Tnfaip3 OTU and ZF4 cells suggests that A20 OTU proteins rescue the aberrant RIP1 ubiquitination and defective homing of A20 ZF4 proteins observed in Tnfaip3 ZF4 and ZF4 cells."
reach
"Tnfaip3 is induced by NF-kappaB signaling as an early response gene and encodes the A20 protein, a ubiquitin modifier that inhibits formation of linear and K63 linked ubiquitin chains on key proteins in the NF-kappaB signaling pathway to provide a negative feedback that terminates further activation of NF-kappaB."
reach
"TNFAIP3 mRNA and protein are rapidly induced by NF-kappaB and form a critical negative feedback loop to diminish NF-kappaB activity by adding K48 linked ubiquitin chains, removing K63 linked ubiquitin chains, and inhibiting the addition of linear ubiquitin chains to key molecules in the NF-kappaB signaling axis."
sparser
"We analyze the network by means of the model combining a deterministic description for molecular species with large cellular concentrations with two classes of stochastic switches: cell-surface receptor activation by TNFalpha ligand, and IkappaBalpha and A20 genes activation by NF-kappaB molecules."