Lactase (LCT), a member of the β-galactosidase family of enzyme, is involved in the hydrolysis of the disaccharide lactose into constituent galactose and glucose monomers. In humans, lactase is present predominantly along the brush border membrane of the differentiated enterocytes lining the villi of the small intestine.
Lactase is essential for digestive hydrolysis of lactose in milk. Deficiency of the enzyme causes lactose intolerance; most humans become lactose intolerant as adults.
Lactase persistence is not due to mutations within the lactase gene, LCT, but to mutations outside the gene in control regions that regulate its expression. They are two intronic variations (C/T and G/A) in the MCM6 gene, MCM6, located approximately 14 kb (-13910) and 22 kb (-22018) upstream of LCT, respectively.Identification of a variant associated with adult-type hypolactasia. Nat Genet 2002;30: 233-7. Free text. PMID 11788828. C/T(-13910) variant has been shown that can function in vitro as a cis element capable of enhancing differential transcriptional activation of LCT promoter.Olds LC, Sibley E. Lactase persistence DNA variant enhances lactase promoter activity in vitro: functional role as a cis regulatory element. Hum Mol Genet 2003 Sep 15; 12(18): 2333-40.'' Free text. PMID 12915462.
Also used to screen for blue white colonies into the MCS of various plasmid vectors in E.Coli or other bacteria, as the lacZ gene is destroyed
Laktase | Lactase | Laktazo | לקטאז | Lactase | Laktaza | Lactase | Laktaasi