DNA Polymorphisms in the Lactase Gene

The enzyme lactase, which is responsible for the digestion of dietary lactose, is present in the intestine of some adults but not others. As a means of providing a platform to explore the molecular basis of this nutritionally relevant genetic variation we have screened for polymorphism in several regions of the lactase gene. In each case simple polymerase chain reaction-based procedures (including single-strand conformation analysis and denaturing gradient gel electrophoresis) were used, combined with silver staining as a method of detection. Allelic variation was found at 6 different sites. One previously published polymorphism was also tested. The frequencies of the alleles were determined in more than 100 unrelated individuals of the Centre d’Etude du Polymorphisme Humain (CEPH) panel, and the haplotypes were deduced. A region of linkage disequilibrium was observed, which spans the whole coding region of the lactase gene (∼ 60–70 kb); there were only 3 common haplotypes in this population. When the CEPH sample was subdivided according to the population of origin (France or Utah) the haplotype frequencies were shown to be markedly different.

[1]  D. Swallow,et al.  Studies on the expression of intestinal lactase in different individuals. , 1995, Gut.

[2]  H. Naim,et al.  The polymorphic expression of lactase in adults is regulated at the messenger RNA level. , 1994, Gastroenterology.

[3]  S. Elbein Linkage disequilibrium among RFLPs at the insulin-receptor locus despite intervening Alu repeat sequences. , 1992, American journal of human genetics.

[4]  W. Boll,et al.  Regulation of intestinal lactase in adult hypolactasia. , 1992, The Journal of clinical investigation.

[5]  H. Büller,et al.  Molecular basis of lactase levels in adult humans. , 1992, The Journal of clinical investigation.

[6]  W. Boll,et al.  Structure of the chromosomal gene and cDNAs coding for lactase-phlorizin hydrolase in humans with adult-type hypolactasia or persistence of lactase. , 1991, American journal of human genetics.

[7]  H. Korsmo,et al.  The biosynthetic basis of adult lactase deficiency. , 1990, The Journal of clinical investigation.

[8]  A. Ballabio,et al.  GENETIC STUDY OF HUMAN ADULT-TYPE HYPOLACTASIA BY ANALYSIS OF RESTRICTION FRAGMENT LENCHT POLYMORPHISHS (RFLPs) OF THE LACTASE GENE , 1990, Pediatric Research.

[9]  D. Swallow,et al.  MOSAIC PATTERN OF LACTASE EXPRESSION BY VILLUS ENTEROCYTES IN HUMAN ADULT-TYPE HYPOLACTASIA , 1990, Pediatric Research.

[10]  H. Cann,et al.  Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome. , 1990, Genomics.

[11]  T. Sekiya,et al.  Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. , 1989, Genomics.

[12]  G. Semenza,et al.  Complete primary structure of human and rabbit lactase‐phlorizin hydrolase: implications for biosynthesis, membrane anchoring and evolution of the enzyme. , 1988, The EMBO journal.

[13]  R. Myers,et al.  Nearly all single base substitutions in DNA fragments joined to a GC-clamp can be detected by denaturing gradient gel electrophoresis. , 1985, Nucleic acids research.

[14]  T McLellan,et al.  Genetic distances between the Utah Mormons and related populations. , 1984, American journal of human genetics.

[15]  G. Flatz Gene-dosage effect on intestinal lactase activity demonstrated in vivo. , 1984, American journal of human genetics.

[16]  S. Povey,et al.  Lactase polymorphism in adult British natives: estimating allele frequencies by enzyme assays in autopsy samples. , 1982, American journal of human genetics.

[17]  F. Sanger,et al.  DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[18]  E. Thompson,et al.  The detection of linkage disequilibrium between closely linked markers: RFLPs at the AI-CIII apolipoprotein genes. , 1988, American journal of human genetics.

[19]  R. Myers,et al.  Detection and localization of single base changes by denaturing gradient gel electrophoresis. , 1987, Methods in enzymology.

[20]  L. Lerman,et al.  Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis. , 1987, Methods in enzymology.

[21]  T. Sahi The inheritance of selective adult-type lactose malabsorption. , 1974, Scandinavian journal of gastroenterology. Supplement.