Defective IRAK4 does not form a complex with MyD88 within the TLR5 complex

Stable Identifier
R-HSA-5602472
Type
Reaction [transition]
Species
Homo sapiens
Related Species
Escherichia coli
Compartment
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Autosomal recessive (AR) IRAK-4 deficiency leads to impaired TLR responses in leukocytes and is associated with increased susceptibility to pyogenic bacterial infections in childhood (Picard C et al. 2003; Medvedev AE et al. 2003; Yamamoto T et al. 2014). Unlike most of the identified gene variants of IRAK4 with nonsense or frame shift mutations that create premature stop codons and result in abolished IRAK4 production, the protein level of missense variant IRAK4 R12C was comparable with wild type (WT) when expressed in human embryonic kidney 293 (HEK293T) cells (Ku CL et al. 2007; Yamamoto T et al. 2014). Analytical gel filtration of recombinant WT or mutant IRAK4 and MyD88 proteins revealed that IRAK4 R12C failed to form a complex with MyD88. These results are in agreement with nuclear magnetic resonance (NMR) titration study that showed a lower affinity of IRAK R12C variant towards 1H-15N-labeled MyD88 N-terminal domain (Yamamoto T et al. 2014).

Literature References
PubMed ID Title Journal Year
17878374 TLR9 activation induces normal neutrophil responses in a child with IRAK-4 deficiency: involvement of the direct PI3K pathway

Hoarau, C, Gérard, B, Lescanne, E, Henry, D, François, S, Lacapère, JJ, El Benna, J, Dang, PM, Grandchamp, B, Lebranchu, Y, Gougerot-Pocidalo, MA, Elbim, C

J. Immunol. 2007
24316379 Functional assessment of the mutational effects of human IRAK4 and MyD88 genes

Yamamoto, T, Tsutsumi, N, Tochio, H, Ohnishi, H, Kubota, K, Kato, Z, Shirakawa, M, Kondo, N

Mol. Immunol. 2014
Participants
Participant Of
Normal reaction
Disease
Name Identifier Synonyms
primary immunodeficiency disease 612 immune deficiency disorder, immunodeficiency syndrome, hypoimmunity
Authored
Reviewed
Created