| Literature DB >> 11788823 |
Ryuta Koishi1, Yosuke Ando, Mitsuru Ono, Mitsuru Shimamura, Hiroaki Yasumo, Toshihiko Fujiwara, Hiroyoshi Horikoshi, Hidehiko Furukawa.
Abstract
The KK obese mouse is moderately obese and has abnormally high levels of plasma insulin (hyperinsulinemia), glucose (hyperglycemia) and lipids (hyperlipidemia). In one strain (KK/San), we observed abnormally low plasma lipid levels (hypolipidemia). This mutant phenotype is inherited recessively as a mendelian trait. Here we report the mapping of the hypolipidemia (hypl) locus to the middle of chromosome 4 and positional cloning of the autosomal recessive mutation responsible for the hypolipidemia. The hypl locus encodes a unique angiopoietin-like lipoprotein modulator, which we named Allm1. It is identical to angiopoietin-like protein 3, encoded by Angptl3, and has a highly conserved counterpart in humans. Overexpression of Angptl3 or intravenous injection of the purified protein in KK/San mice elicited an increase in circulating plasma lipid levels. This increase was also observed in C57BL/6J normal mice. Taken together, these data suggest that Angptl3 regulates lipid metabolism in animals.Entities:
Mesh:
Substances:
Year: 2002 PMID: 11788823 DOI: 10.1038/ng814
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330