Characterization of the RDC1 gene which encodes the canine homolog of a proposed human VIP receptor. Expression does not correlate with an increase in VIP binding sites.

Abstract:

:We have isolated a portion of the canine gene encoding the orphan receptor RDC1 [1]. The complete coding sequence is contained in a single exon, and an intron divides the 5' untranslated region of RDC1 mRNA. The RDC1 protein is 94% homologous to the gene product of GPRN1, which has been proposed to serve as a VIP receptor when expressed in CHO-K1 and COS-7 cells (Sreedharan, S.P. et al. (1991) Proc. Natl. Acad. Sci. USA 88, 4986-4990). Northern analysis indicates that CHO-K1 cells endogenously express a 2.1 kb RDC1 mRNA. However, while CHO-K1 cells possess detectable low affinity [125I]VIP binding sites, VIP binding is not altered in membranes of CHO-K1 cells expressing varying amounts of the RDC1 gene construct. Further, endogenous VIP binding is not increased by transient expression of RDC1 in COS-7 cells. Taken together, the data suggest that RDC1 is not a canine homolog of the proposed VIP receptor.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Cook JS,Wolsing DH,Lameh J,Olson CA,Correa PE,Sadee W,Blumenthal EM,Rosenbaum JS

doi

10.1016/0014-5793(92)80184-i

keywords:

subject

Has Abstract

pub_date

1992-03-30 00:00:00

pages

149-52

issue

2

eissn

0014-5793

issn

1873-3468

pii

0014-5793(92)80184-I

journal_volume

300

pub_type

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