Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia by Péterfy Miklós, Ben-Zeev Osnat, Mao Hui Z, Weissglas-Volkov Daphna, Aouizerat Bradley E, Pullinger Clive R, Frost Philip H, Kane John P, Malloy Mary J, Reue Karen, Pajukanta Päivi, Doolittle Mark H in Nature genetics (2007). PubMed

Abstract

Hypertriglyceridemia is a hallmark of many disorders, including metabolic syndrome, diabetes, atherosclerosis and obesity. A well-known cause is the deficiency of lipoprotein lipase (LPL), a key enzyme in plasma triglyceride hydrolysis. Mice carrying the combined lipase deficiency (cld) mutation show severe hypertriglyceridemia owing to a decrease in the activity of LPL and a related enzyme, hepatic lipase (HL), caused by impaired maturation of nascent LPL and hepatic lipase polypeptides in the endoplasmic reticulum (ER). Here we identify the gene containing the cld mutation as Tmem112 and rename it Lmf1 (Lipase maturation factor 1). Lmf1 encodes a transmembrane protein with an evolutionarily conserved domain of unknown function that localizes to the ER. A human subject homozygous for a deleterious mutation in LMF1 also shows combined lipase deficiency with concomitant hypertriglyceridemia and associated disorders. Thus, through its profound effect on lipase activity, LMF1 emerges as an important candidate gene in hypertriglyceridemia.

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