The human ATP-binding cassette half transporter G1 (hABCG1) may play a role
in cholesterol transport in macrophages, Using RACE assays we determined t
he structure of this gene. The hABCG1 gene spans more than 97 kb comprising
20 exons, 20 kb and 5 exons more than hitherto described. Four of the nove
l exons are upstream and one is downstream of previous exon 1, and they are
predicted to encode at least five novel transcripts. We also detected two
separate promoters, upstream of exons 1 and 5, respectively. The region 650
bp upstream of exon I was predicted to contain putative binding sites for
SP1 and nuclear factor kappaB (NF-kappaB), but no sterol response elements
(SREs) or retinoid X receptor (RXR) binding sites. The region 650 bp upstre
am of exon 5 contained 19 possible SP1 binding sites, one possible SRE, two
possible NF-kappaB, and two putative RXR binding sites. Nevertheless, both
promoters responded in macrophages to stimulation by hydroxy-cholesterol a
nd retinoic acid. (C) 2001 Academic Press.