The leptin receptor promoter controls expression of a second distinct protein

B Bailleul, I Akerblom, AD Strosberg - Nucleic acids research, 1997 - academic.oup.com
B Bailleul, I Akerblom, AD Strosberg
Nucleic acids research, 1997academic.oup.com
The leptin receptor (OB-R) is a single membrane-spanning protein that mediates the weight-
regulatory effects of leptin (OB protein). Several mRNA splice variants have been described
which either encode OB-R proteins with cytoplasmic domains of different length or the OB-R
and B219/OBR variants, which have different 5′-untranslated regions. Here we report
evidence for the synthesis of a human mRNA splice variant of the OB-R gene that potentially
encodes a novel protein, leptin receptor gene-related protein (OB-RGRP), which displays no …
Abstract
The leptin receptor (OB-R) is a single membrane-spanning protein that mediates the weight-regulatory effects of leptin (OB protein). Several mRNA splice variants have been described which either encode OB-R proteins with cytoplasmic domains of different length or the OB-R and B219/OBR variants, which have different 5′-untranslated regions. Here we report evidence for the synthesis of a human mRNA splice variant of the OB-R gene that potentially encodes a novel protein, leptin receptor gene-related protein (OB-RGRP), which displays no sequence similarity to the leptin receptor itself. This OB-RGRP transcript contains the first two OB-R gene 5′-untranslated exons, but then is alternatively spliced to two novel exons which were mapped to a yeast artificial chromosome containing the leptin receptor gene. First identified by analysis of a large human expressed sequence tag database, the OB-RGRP transcript has now also been found in human and mouse tissues by the use of PCR. Preliminary experiments suggest that OB-RGRP and the OB-R variants share similar patterns of expression that are distinct from that of the B219/OBR variant. OB-RGRP is highly homologous to putative open reading frames in both yeast and Caenorhabditis elegans, suggesting a phylogenetically conserved role for this novel protein.
Oxford University Press