Literature DB >> 7823249

Racial variation in the O-acetylation phenotype of human colonic mucosa.

F Campbell1, M A Appleton, C E Fuller, M P Greeff, J Hallgrimsson, R Katoh, O L Ng, A Satir, G T Williams, E D Williams.   

Abstract

O-acetylated and non-O-acetylated sialoglycoproteins can be distinguished by the mPAS (mild periodic acid-Schiff) histochemical technique. Individual adults show one of three different patterns of staining of large intestinal mucosa: uniformly mPAS-positive, uniformly mPAS-negative, or mPAS-negative with scattered mPAS-positive crypts. To test our hypothesis that these variations are the result of a single autosomal gene (oat) polymorphism, we have studied the frequency of the three patterns of staining in a total of 435 adult colon specimens from six geographically separate populations: British, South African blacks, Icelanders, Japanese, Hong Kong Chinese, and Bahrainis. The distribution of the three types of staining fell into two groups. In Japanese and Chinese, uniformly mPAS-positive cases were much more frequent than uniformly mPAS-negative cases; this distribution differed significantly (chi 2, P < 0.001) from that in non-Sino-Japanese, where the uniformly mPAS-positive phenotype was much less frequently found than the uniformly mPAS-negative phenotype. In neither of the groups did the frequency of the three phenotypes differ significantly from that predicted for a single gene polymorphism by the Hardy-Weinberg law. The variation in staining patterns between populations is consistent with variation in frequency of a single polymorphic autosomal gene (oat) controlling O-acetylation of sialic acid, probably by an O-acetyl transferase enzyme. Loss of function mutation in the high acetylator gene (oata) in a colonic crypt stem cell in heterozygous individuals would account for the scattered discordant crypts. Gene frequencies for a variety of enzymes differ between the Sino-Japanese and non-Sino-Japanese races.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1994        PMID: 7823249     DOI: 10.1002/path.1711740305

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  12 in total

1.  Reduction of sialic acid O-acetylation in human colonic mucins in the adenoma-carcinoma sequence.

Authors:  A P Corfield; N Myerscough; B F Warren; P Durdey; C Paraskeva; R Schauer
Journal:  Glycoconj J       Date:  1999-06       Impact factor: 2.916

2.  Tumor burden and clonality in multiple intestinal neoplasia mouse/normal mouse aggregation chimeras.

Authors:  M R Novelli; H Wasan; I Rosewell; J Bee; I P Tomlinson; N A Wright; W F Bodmer
Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-26       Impact factor: 11.205

3.  Histochemical alterations of mucin in normal colon, inflammatory bowel disease and colonic adenocarcinoma.

Authors:  D A Owen; P E Reid
Journal:  Histochem J       Date:  1995-11

4.  Post-irradiation somatic mutation and clonal stabilisation time in the human colon.

Authors:  F Campbell; G T Williams; M A Appleton; M F Dixon; M Harris; E D Williams
Journal:  Gut       Date:  1996-10       Impact factor: 23.059

Review 5.  The Densely O-Glycosylated MUC2 Mucin Protects the Intestine and Provides Food for the Commensal Bacteria.

Authors:  Liisa Arike; Gunnar C Hansson
Journal:  J Mol Biol       Date:  2016-02-12       Impact factor: 5.469

6.  Characterization of O-acetylation in sialoglycans by MALDI-MS using a combination of methylamidation and permethylation.

Authors:  Zhaoguan Wu; Henghui Li; Qiwei Zhang; Xin Liu; Qi Zheng; Jianjun Li
Journal:  Sci Rep       Date:  2017-04-07       Impact factor: 4.379

7.  Modified Sialic Acids on Mucus and Erythrocytes Inhibit Influenza A Virus Hemagglutinin and Neuraminidase Functions.

Authors:  Karen N Barnard; Brynn K Alford-Lawrence; David W Buchholz; Brian R Wasik; Justin R LaClair; Hai Yu; Rebekah Honce; Stefan Ruhl; Petar Pajic; Erin K Daugherity; Xi Chen; Stacey L Schultz-Cherry; Hector C Aguilar; Ajit Varki; Colin R Parrish
Journal:  J Virol       Date:  2020-04-16       Impact factor: 5.103

8.  Normal colonic mucosa in hereditary non-polyposis colorectal cancer shows no generalised increase in somatic mutation.

Authors:  G T Williams; J M Geraghty; F Campbell; M A Appleton; E D Williams
Journal:  Br J Cancer       Date:  1995-05       Impact factor: 7.640

Review 9.  Enzymatic Adaptation of Bifidobacterium bifidum to Host Glycans, Viewed from Glycoside Hydrolyases and Carbohydrate-Binding Modules.

Authors:  Toshihiko Katoh; Miriam N Ojima; Mikiyasu Sakanaka; Hisashi Ashida; Aina Gotoh; Takane Katayama
Journal:  Microorganisms       Date:  2020-03-28

10.  Fixation and Spread of Somatic Mutations in Adult Human Colonic Epithelium.

Authors:  Anna M Nicholson; Cora Olpe; Alice Hoyle; Ann-Sofie Thorsen; Teja Rus; Mathilde Colombé; Roxanne Brunton-Sim; Richard Kemp; Kate Marks; Phil Quirke; Shalini Malhotra; Rogier Ten Hoopen; Ashraf Ibrahim; Cecilia Lindskog; Meagan B Myers; Barbara Parsons; Simon Tavaré; Mark Wilkinson; Edward Morrissey; Douglas J Winton
Journal:  Cell Stem Cell       Date:  2018-05-17       Impact factor: 24.633

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