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J. Biol. Chem., Vol. 275, Issue 39, 29946-29954, September 29, 2000
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From Immunex Corp., Seattle, Washington 98101
Two novel members of the interleukin-1 receptor
(IL-1R) family, identified by homology searches of human genomic
sequence data bases, are described. The genes have been named according to their structural features: TIGIRR-1
(three immunoglobulin
domain-containing IL-1
receptor-related) and TIGIRR-2.
TIGIRR-2 has recently been identified as causing mental
retardation when mutated (Carrie, A., Jun, L., Bienvenu, T., Vinet,
M. C., McDonell, N., Couvert, P., Zemni, R., Cardona, A., Van
Buggenhout, G., Frints, S., Hamel, B., Moraine, C., Ropers, H. H.,
Strom, T., Howell, G. R., Whittaker, A., Ross, M. T., Kahn,
A., Fryns, J. P., Beldjord, C., Marynen, P., and Chelly, J. (1999)
Nat. Genet. 23, 25-31) and called
IL1RAPL, a name we will also use henceforth. Neither
receptor alone was able to mediate transcriptional activation of
NF-
B in response to IL-1
, IL-1
, or IL-18. In order to begin to
elucidate the function of these and other orphan IL-1R family members,
we have developed a functional assay utilizing a panel of chimeric
receptors containing the extracellular and transmembrane domains of
either type I IL-1R or IL-1R accessory protein (AcP) coupled to the
cytoplasmic domains of all family members. Coexpression of each IL-1R
chimera with each AcP chimera and an NF-
B-responsive reporter
demonstrated that the cytoplasmic domains could be classified as
IL-1R-like, AcP-like, or neither. Any IL-1R-like cytoplasmic domain
could cooperate with any AcP-like cytoplasmic domain. The TIGIRR-1 and IL1RAPL cytoplasmic domains, however, were unable to signal as either
IL-1R-like or AcP-like components, suggesting that they function as a
new class of receptors within this family.
The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AF284433 (murine IL-1Rrp2), AF284434 (human IL1Rrp2), AF284435 (human TIGIRR-2/IL1RAPL), AF284436 (human TIGIRR-1), and AF284437 (murine TIGIRR-1).
To whom correspondence should be addressed: Immunex Corp., 51 University St., Seattle, WA 98101. Tel.: 206-389-4005; Fax: 206-233-9733; E-mail: simsj@immunex.com.
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