Lactose digestion and the evolutionary genetics of lactase persistence.

Abstract:

:It has been known for some 40 years that lactase production persists into adult life in some people but not in others. However, the mechanism and evolutionary significance of this variation have proved more elusive, and continue to excite the interest of investigators from different disciplines. This genetically determined trait differs in frequency worldwide and is due to cis-acting polymorphism of regulation of lactase gene expression. A single nucleotide polymorphism located 13.9 kb upstream from the lactase gene (C-13910 > T) was proposed to be the cause, and the -13910*T allele, which is widespread in Europe was found to be located on a very extended haplotype of 500 kb or more. The long region of haplotype conservation reflects a recent origin, and this, together with high frequencies, is evidence of positive selection, but also means that -13910*T might be an associated marker, rather than being causal of lactase persistence itself. Doubt about function was increased when it was shown that the original SNP did not account for lactase persistence in most African populations. However, the recent discovery that there are several other SNPs associated with lactase persistence in close proximity (within 100 bp), and that they all reside in a piece of sequence that has enhancer function in vitro, does suggest that they may each be functional, and their occurrence on different haplotype backgrounds shows that several independent mutations led to lactase persistence. Here we provide access to a database of worldwide distributions of lactase persistence and of the C-13910*T allele, as well as reviewing lactase molecular and population genetics and the role of selection in determining present day distributions of the lactase persistence phenotype.

journal_name

Hum Genet

journal_title

Human genetics

authors

Ingram CJ,Mulcare CA,Itan Y,Thomas MG,Swallow DM

doi

10.1007/s00439-008-0593-6

subject

Has Abstract

pub_date

2009-01-01 00:00:00

pages

579-91

issue

6

eissn

0340-6717

issn

1432-1203

journal_volume

124

pub_type

杂志文章
  • Extended polymorphism of the human esterase D isozyme system: description of a "new" allele EsD*11.

    abstract::Using "new" techniques (malic acid thin layer agarose gel electrophoresis and/or isoelectric focusing), the polymorphism of the human red cell isozyme system esterase D (ESD) was shown to be extended. We report the gene frequencies observed among 312 unrelated Caucasian individuals living in the Düsseldorf area. The f...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00292672

    authors: Henke J,Schweitzer H,Bär W,Weidinger S,Weissmann J,Baur MP

    更新日期:1986-05-01 00:00:00

  • Genetic changes in mammalian cells reminiscent of an SOS response.

    abstract::Prior to the isolation of mammalian DNA repair genes and identification of their gene products, the comparison between the bacterial SOS response and various similar reactions in mammalian cells remains rather speculative. The increasing number of observed phenomena including enhanced DNA repair, virus induction, indu...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00291392

    authors: Herrlich P,Mallick U,Ponta H,Rahmsdorf HJ

    更新日期:1984-01-01 00:00:00

  • Molecular analysis of chromosome region 11p13 in patients with Drash syndrome.

    abstract::The association of nephropathy, Wilms' tumour and genital abnormalities is known as Drash syndrome. Two of these features are also seen in the WAGR (Wilms' tumour, aniridia, genito-urinary abnormalities, mental retardation) complex, known to be associated with deletions of chromosome region 11p13. We have carried out ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00194641

    authors: Jadresic L,Wadey RB,Buckle B,Barratt TM,Mitchell CD,Cowell JK

    更新日期:1991-03-01 00:00:00

  • Renin locus restriction fragment length polymorphism.

    abstract::The use of two genomic EcoRI fragments as probes is discussed. ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00291180

    authors: Chen LZ,Easteal S

    更新日期:1989-06-01 00:00:00

  • Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome.

    abstract::A young female was diagnosed as having X-linked muscular dystrophy of the Duchenne type. Chromosome studies, including trypsin-Giemsa banding, Quinacrine fluorescence, and nucleolus organizer region (NOR) silver staining revealed an X-autosome reciprocal translocation t(X;21) (p21;p12). Utilizing both [3H] thymidine a...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00270570

    authors: Verellen-Dumoulin C,Freund M,De Meyer R,Laterre C,Frédéric J,Thompson MW,Markovic VD,Worton RG

    更新日期:1984-01-01 00:00:00

  • Indirect immunofluorescence of inactive centromeres as indicator of centromeric function.

    abstract::Two previous single case reports from the literature showed the presence or absence of centromeric antigens at the site of the inactive centromeres in one (X;X) and in one (9;11) dicentric chromosome. We studied nine different dicentric chromosomes using anticentromeric antibodies and immunofluorescence techniques. In...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00292655

    authors: Peretti D,Maraschio P,Lambiase S,Lo Curto F,Zuffardi O

    更新日期:1986-05-01 00:00:00

  • A unified GMDR method for detecting gene-gene interactions in family and unrelated samples with application to nicotine dependence.

    abstract::Gene-gene and gene-environment interactions govern a substantial portion of the variation in complex traits and diseases. In convention, a set of either unrelated or family samples are used in detection of such interactions; even when both kinds of data are available, the unrelated and the family samples are analyzed ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s00439-013-1361-9

    authors: Chen GB,Liu N,Klimentidis YC,Zhu X,Zhi D,Wang X,Lou XY

    更新日期:2014-02-01 00:00:00

  • Assignment of the structural gene coding for albumin to human chromosome 4.

    abstract::Albumin is a developmentally regulated serum protein synthesized in the liver mainly during adulthood. Family studies using variant forms of albumin established autosomal linkage between albumin and group-specific component protein (GS). Since GC has been assigned to human chromosome 4, albumin can be indirectly assig...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00304551

    authors: Kao FT,Hawkins JW,Law ML,Dugaiczyk A

    更新日期:1982-01-01 00:00:00

  • Assignment of the human hap retinoic acid receptor RAR beta gene to the p24 band of chromosome 3.

    abstract::The human hap retinoic acid receptor RAR beta has been localized by in situ hybridization to the p24 band of chromosome 3. ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00702867

    authors: Mattei MG,de Thé H,Mattei JF,Marchio A,Tiollais P,Dejean A

    更新日期:1988-10-01 00:00:00

  • Rapid detection of alpha-1-antitrypsin deficiency by analysis of a PCR-induced TaqI restriction site.

    abstract::A single base substitution is responsible for the PI-Z mutation in alpha-1-antitrypsin (AAT) deficiency. The Z mutation, which is in exon V of the AAT gene, was analysed directly using a primer designed with a single base substitution in the DNA sequence. During the polymerase chain reaction with this primer, a restri...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00201739

    authors: Dry PJ

    更新日期:1991-10-01 00:00:00

  • Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria.

    abstract::Eight polymorphic restriction enzyme sites at the phenylalanine hydroxylase (PAH) locus were analyzed from the parental chromosomes in 33 Danish nuclear families with at least one phenylketonuric (PKU) child. Determination of haplotypes of 66 normal chromosomes and 66 chromosomes bearing mutant allele(s) demonstrated ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00283048

    authors: Chakraborty R,Lidsky AS,Daiger SP,Güttler F,Sullivan S,Dilella AG,Woo SL

    更新日期:1987-05-01 00:00:00

  • Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism.

    abstract::Various genetic loci harboring oncogenes, tumor suppressor genes, and genes for calcium receptors have been implicated in the development of parathyroid tumors. We have carried out loss of heterozygosity (LOH) studies in chromosomes 1p, 1q, 3q, 6q, 11q, 13q, 15q, and X in a total of 89 benign parathyroid tumors. Of th...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s004390050369

    authors: Farnebo F,Teh BT,Dotzenrath C,Wassif WS,Svensson A,White I,Betz R,Goretzki P,Sandelin K,Farnebo LO,Larsson C

    更新日期:1997-03-01 00:00:00

  • Retinoblastoma: host resistance and 13q- chromosomal deletion.

    abstract::Data for 27 cases of retinoblastoma that developed in patients with 13q- were collected from the literature and analyzed. The distribution of unilateral and bilateral cases of retinoblastoma differed significantly from the expectation that the degree of expressivity does not differ between the retinoblastoma gene and ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00281568

    authors: Matsunaga E

    更新日期:1980-01-01 00:00:00

  • Genetic heterogeneity of severe von Willebrand disease type III in the German population.

    abstract::The genetic heterogeneity of severe von Willebrand disease (vWd) type III was estimated by analysing extended haplotypes of eleven intragenic restriction fragment length polymorphisms and one variable number of tandem repeat polymorphism in 32 patients from 28 families from Germany or of German origin. All patients we...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00206958

    authors: Schneppenheim R,Krey S,Bergmann F,Bock D,Budde U,Lange M,Linde R,Mittler U,Meili E,Mertes G

    更新日期:1994-12-01 00:00:00

  • A novel polymorphism in the coding region of CYBB, the human gp91-phox gene.

    abstract::We have identified a rare polymorphism (G to C at nucleotide 1102) in CYBB, which codes for gp91-phox, a component of NADPH oxidase. Polymorphonuclear leukocytes with this enzyme produced normal amounts of superoxide anion. ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF02281870

    authors: Kuribayashi F,de Boer M,Leusen JH,Verhoeven AJ,Roos D

    更新日期:1996-05-01 00:00:00

  • Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphate.

    abstract::Mutual correction of co-cultivated fibroblasts from patients with Hunter's and Hurler's syndrome could be inhibited by either fructose 1-phosphate or mannose 6-phosphate. In the presence of fructose 1-phosphate a 50% mixture of fibroblasts from a patient with Hunter's syndrome and a normal homozygous individual showed...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00569706

    authors: Tønnesen T,Lykkelund C,Güttler F

    更新日期:1982-01-01 00:00:00

  • Correlation between human papillomavirus-associated cervical cancer and p53 codon 72 arginine/proline polymorphism.

    abstract::High-risk mucosal human papillomaviruses encode an E6 oncoprotein, which binds the cellular p53 tumor suppressor protein, thereby marking it for degradation through the ubiquitin-mediated pathway. A common p53 polymorphism at codon-72 of exon 4 results in translation to either arginine or proline. Recently reported da...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s004399900138

    authors: Tachezy R,Mikysková I,Saláková M,Van Ranst M

    更新日期:1999-12-01 00:00:00

  • Disruption of long-range gene regulation in human genetic disease: a kaleidoscope of general principles, diverse mechanisms and unique phenotypic consequences.

    abstract::The precise control of gene expression programs is crucial for the establishment of the diverse gene activity patterns required for the correct development, patterning and differentiation of the myriad of cell types within an organism. The crucial importance of non-coding regions of the genome in the control of gene r...

    journal_title:Human genetics

    pub_type: 杂志文章,评审

    doi:10.1007/s00439-014-1424-6

    authors: Bhatia S,Kleinjan DA

    更新日期:2014-07-01 00:00:00

  • South Korea: in the midst of a privacy reform centered on data sharing.

    abstract::With rapid developments in genomic and digital technologies, genomic data sharing has become a key issue for the achievement of precision medicine in South Korea. The legal and administrative framework for data sharing and protection in this country is currently under intense scrutiny from national and international s...

    journal_title:Human genetics

    pub_type: 杂志文章,评审

    doi:10.1007/s00439-018-1920-1

    authors: Kim H,Kim SY,Joly Y

    更新日期:2018-08-01 00:00:00

  • TaqI HLA-B and -DRB RFLP analysis can predict disease in siblings of affected children with 21-hydroxylase deficiency.

    abstract::The possibility of using TaqI restriction fragment length polymorphism (RFLP) analysis of the HLA-B locus and the HLA-DR-DQ subregions, flanking the 21-hydroxylase genes, for predicting disease in siblings of children with 21-hydroxylase deficiency was analyzed in 12 nuclear families with at least one affected child a...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00194218

    authors: Olerup O,Luthman H,Ritzén EM,Haglund-Stengler B

    更新日期:1990-10-01 00:00:00

  • A human gene similar to Drosophila melanogaster peanut maps to the DiGeorge syndrome region of 22q11.

    abstract::A Drosophila-related expressed sequence tag (DRES) with sequence similarity to the peanut gene has previously been localized to human chromosome 22q11. We have isolated the cDNA corresponding to this DRES and show that it is a novel member of the family of septin genes, which encode proteins with GTPase activity thoug...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s004390050576

    authors: McKie JM,Sutherland HF,Harvey E,Kim UJ,Scambler PJ

    更新日期:1997-11-01 00:00:00

  • Exclusion of the phosphoinositide-specific phospholipase C beta 3 (PLCB3) gene as a candidate for multiple endocrine neoplasia type 1.

    abstract::The predisposing genetic defect in multiple endocrine neoplasia type 1 has been assigned to chromosomal region 11q13. Our previous attempts to identify the MEN1 gene have resulted in the isolation of the phospholipase C beta 3 gene from the actual region. PLCB3 plays an important role in signal transduction and, moreo...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s004390050326

    authors: Weber G,Grimmond S,Lagercrantz J,Friedman E,Phelan C,Carson E,Hayward N,Jacobovitz O,Nordenskjöld M,Larsson C

    更新日期:1997-01-01 00:00:00

  • Inbreeding in recessive diseases.

    abstract::The consanguinity of parents (born in France) of individuals who have a recessive disease has been studied. The frequency of first cousin marriages is less than 0.2% in the general French population. Among the parents of affected individuals the following frequencies of first cousin matings were observed: cystic fibro...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00527398

    authors: Tchen P,Bois E,Feingold J,Feingold N,Kaplan J

    更新日期:1977-09-22 00:00:00

  • A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome.

    abstract::We have isolated an X chromosome probe, St35.691 (DXS305), which detects two RFLPs with TaqI and PstI, whose combined heterozygosity is about 60%. This probe has been assigned to Xq28 by physical and genetic mapping and is very closely linked to DXS52, DXS15, and the coagulation factor VIII gene (F8C). The best estima...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00288280

    authors: Vincent A,Kretz C,Oberlé I,Mandel JL

    更新日期:1989-04-01 00:00:00

  • Effect of nonsense mutations on PTEN mRNA stability.

    abstract::Cowden disease is an autosomal dominant disorder associated with an elevated risk of breast, thyroid and skin cancers, in which germline mutations of a tumour suppressor gene (PTEN) have been identified. PTEN has a dual-specificity tyrosine phosphatase domain thought to be essential for tumour suppression. Previous ge...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s004390000317

    authors: Raizis AM,Ferguson MM,George PM

    更新日期:2000-07-01 00:00:00

  • A molecular genetic approach to the identification of isochromosomes of chromosome 21.

    abstract::The largest class of de novo chromosomal rearrangements in Down syndrome are rea(21q21q). Classically, these rearrangements have been termed Robertsonian translocations, implying an attachment of two different chromosome 21 homologues. Additionally, a Robertsonian translocation between two chromosomes 21 cannot be dis...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00201838

    authors: Shaffer LG,Jackson-Cook CK,Meyer JM,Brown JA,Spence JE

    更新日期:1991-02-01 00:00:00

  • The CLCA gene locus as a modulator of the gastrointestinal basic defect in cystic fibrosis.

    abstract::To determine whether the CLCA gene family of calcium-activated chloride channels is a modulator of the basic defect of cystic fibrosis (CF), an association study was performed with polymorphic microsatellite markers covering a 40-Mbp region spanning the CLCA gene locus on human chromosome 1p in CF patients displaying ...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/s00439-004-1190-y

    authors: Ritzka M,Stanke F,Jansen S,Gruber AD,Pusch L,Woelfl S,Veeze HJ,Halley DJ,Tümmler B

    更新日期:2004-11-01 00:00:00

  • Hereditary spastic paraplegia: mitochondrial metalloproteases of yeast.

    abstract::Hereditary spastic paraplegia (HSP) is a genetically heterogenous group of inherited neurodegenerative disorders. Recently, an autosomal recessive form of HSP was mapped to 16q24.3, and subsequently the defective gene associated to HSP was identified and designated SPG7. The SPG7 gene product was predicted to encode a...

    journal_title:Human genetics

    pub_type: 杂志文章,评审

    doi:10.1007/s004390050985

    authors: Pearce DA

    更新日期:1999-06-01 00:00:00

  • Assigning the polymorphic human insulin gene to the short arm of chromosome 11 by chromosome sorting.

    abstract::We have determined the subchromosomal location of the human insulin gene by analyzing DNA isolated from sorted human metaphase chromosomes. Metaphase chromosome suspensions were sorted into fractions according to relative Hoechst fluorescence intensity by the fluorescence activated chromosome sorter. The chromosomal D...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00281255

    authors: Lebo RV,Kan YW,Cheung MC,Carrano AV,Yu LC,Chang JC,Cordell B,Goodman HM

    更新日期:1982-01-01 00:00:00

  • Translocation t(1;17)(q12;q25) with a clinical picture like of a proximal deletion of 1q: identification by in situ hybridization with chromosome 1-specific satellite DNA probes.

    abstract::The authors report a case of a balanced 1;17 translocation with breakpoints located in the secondary constriction of chromosome 1. This translocation is associated with pathological symptoms similar to those observed following a proximal deletion of 1q. We request contact with colleques who have observed similar, or r...

    journal_title:Human genetics

    pub_type: 杂志文章

    doi:10.1007/BF00197700

    authors: Vorsanova SG,Yurov YB,Kurbatov MB,Kazantzeva LZ

    更新日期:1990-12-01 00:00:00