Literature DB >> 1671849

A new deletion polymorphism at D5S71 raises the linkage information on adenomatous polyposis coli: implications for presymptomatic diagnosis.

C M Tops1, C Breukel, H M van der Klift, I S von Leeuwen, J T Wijnen, G Griffioen, H F Vasen, F C den Hartog Jager, F M Nagengast, C B Lamers.   

Abstract

Two independent study-groups, one in Britain and the other in the United States, were the first to report linkage between APC and a TaqI restriction fragment length polymorphism (RFLP) at D5S71 (probe C11p11) on chromosome 5q. They found no recombinants in about 50 informative meioses. The same TaqI RFLP was found to be uninformative for linkage in 15 Dutch polyposis families. The recently reported four base-pair deletion polymorphism (DEL1) at D5S71 has raised the polymorphism information content of this marker from 0.17 to 0.40 in the Dutch population. Seven of 20 polyposis families screened for the DEL1 as well as the TaqI polymorphism gave a combined peak lod score of 5.68 with no recombinants in 37 informative meioses. These data, together with those so far reported in the literature, raise the peak lod score to 17.09 at a recombination fraction of 0.05, the 95% upper confidence limit being 0.09. In combination with the use of another informative marker, D5S81 (probe YN5.48) closely mapping on the other side of APC, the presymptomatic diagnosis of the disease can be made with more than 99.9% certainty. It has to be stressed, however, that the the possible existence of more than one polyposis locus cannot, as yet, be excluded.

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Year:  1991        PMID: 1671849     DOI: 10.1007/bf00201835

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  16 in total

1.  Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5.

Authors:  Y Nakamura; M Lathrop; M Leppert; M Dobbs; J Wasmuth; E Wolff; M Carlson; E Fujimoto; K Krapcho; T Sears
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

2.  Four-base-pair deletion polymorphism at D5S71 (C11p11) linked to APC in the human chromosome 5q21-q22 region.

Authors:  C Breukel; C M Tops; P M Khan
Journal:  Nucleic Acids Res       Date:  1989-12-25       Impact factor: 16.971

Review 3.  Familial polyposis coli.

Authors:  S Bülow
Journal:  Dan Med Bull       Date:  1987-03

4.  Genetic prediction in X-linked agammaglobulinaemia.

Authors:  Y L Lau; R J Levinsky; S Malcolm; J Goodship; R Winter; M Pembrey
Journal:  Am J Med Genet       Date:  1988-10

5.  Report of the Committee on Methods of Linkage Analysis and Reporting.

Authors:  P M Conneally; J H Edwards; K K Kidd; J M Lalouel; N E Morton; J Ott; R White
Journal:  Cytogenet Cell Genet       Date:  1985

6.  Familial polyposis coli.

Authors:  M A Aldred; M Rees; K Tsioupra; S E Leigh; K F Neale; J D Delhanty
Journal:  Lancet       Date:  1988-09-03       Impact factor: 79.321

7.  Localization of the gene for familial adenomatous polyposis on chromosome 5.

Authors:  W F Bodmer; C J Bailey; J Bodmer; H J Bussey; A Ellis; P Gorman; F C Lucibello; V A Murday; S H Rider; P Scambler
Journal:  Nature       Date:  1987 Aug 13-19       Impact factor: 49.962

8.  Congenital hypertrophy of the retinal pigment epithelium predicts colorectal polyposis in Gardner's syndrome.

Authors:  E I Traboulsi; I H Maumenee; A J Krush; D Alcorn; F M Giardiello; R W Burt; J P Hughes; S R Hamilton
Journal:  Arch Ophthalmol       Date:  1990-04

9.  Hyperpigmented lesions of the retinal pigment epithelium in familial adenomatous polyposis.

Authors:  R H Baker; M H Heinemann; H H Miller; J J DeCosse
Journal:  Am J Med Genet       Date:  1988-10

10.  Close linkage of a highly polymorphic marker (D5S37) to familial adenomatous polyposis (FAP) and confirmation of FAP localization on chromosome 5q21-q22.

Authors:  P Meera Khan; C M Tops; M vd Broek; C Breukel; J T Wijnen; M Oldenburg; J vd Bos; I S van Leeuwen-Cornelisse; H F Vasen; G Griffioen
Journal:  Hum Genet       Date:  1988-06       Impact factor: 4.132

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  3 in total

1.  The use of DNA from paraffin wax preserved tissue for predictive diagnosis in familial adenomatous polyposis.

Authors:  D G Morton; F Macdonald; M B Cachon-Gonzales; P M Rindl; J P Neoptolemos; M R Keighley; J D Delhanty; C M McKeown; M Kilpatrick; M A Hultén
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

2.  Predictive diagnosis of familial adenomatous polyposis with linked DNA markers: population based study.

Authors:  F MacDonald; D G Morton; P M Rindl; J Haydon; R Cullen; J Gibson; J P Neoptolemos; M R Keighley; C M McKeown; M Hultén
Journal:  BMJ       Date:  1992-04-04

3.  Presymptomatic diagnosis in families with adenomatous polyposis using highly polymorphic dinucleotide CA repeat markers flanking the APC gene.

Authors:  W A Eckert; C Jung; G Wolff
Journal:  J Med Genet       Date:  1994-06       Impact factor: 6.318

  3 in total

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