Literature DB >> 7913866

Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.

M Mannens1, J M Hoovers, E Redeker, M Verjaal, A P Feinberg, P Little, M Boavida, N Coad, M Steenman, J Bliek.   

Abstract

Cytogenetic and DNA analyses of patients with the Beckwith-Wiedemann syndrome (BWS) enabled us to refine the localization of the syndrome at 11p15.3-pter to two distinct regions. One chromosome region (BWSCR1) is near the insulin (INS) and insulin-like growth factor 2 (IGF2) genes. The other region (BWSCR2) is more proximal near two sequences with zinc-binding finger motifs and a number of known and putative genes. This latter region, at least, seems to be associated with the development of childhood tumors. Our results strongly support the proposed involvement of parental imprinting in the etiology of BWS since all balanced chromosomal abnormalities in these patients were maternally transmitted while the mothers were phenotypically normal. We demonstrate that such an autosomal balanced rearrangement can lead to a specific maternal hypomethylation of the INS/IGF2 genes localized distal to the breakpoint. This underlines the role of these genes in the etiology of the syndrome.

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Year:  1994        PMID: 7913866     DOI: 10.1159/000472337

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  20 in total

Review 1.  Mechanisms of genomic imprinting.

Authors:  K Pfeifer
Journal:  Am J Hum Genet       Date:  2000-09-05       Impact factor: 11.025

2.  Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting.

Authors:  M P Lee; M R DeBaun; K Mitsuya; H L Galonek; S Brandenburg; M Oshimura; A P Feinberg
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-27       Impact factor: 11.205

3.  Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome.

Authors:  M P Lee; M DeBaun; G Randhawa; B A Reichard; S J Elledge; A P Feinberg
Journal:  Am J Hum Genet       Date:  1997-08       Impact factor: 11.025

4.  Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors.

Authors:  D O'Keefe; D Dao; L Zhao; R Sanderson; D Warburton; L Weiss; K Anyane-Yeboa; B Tycko
Journal:  Am J Hum Genet       Date:  1997-08       Impact factor: 11.025

5.  Diagnosing Friedreich's ataxia.

Authors:  N W Wood
Journal:  Arch Dis Child       Date:  1998-03       Impact factor: 3.791

6.  Growing interest in overgrowth.

Authors:  T Cole
Journal:  Arch Dis Child       Date:  1998-03       Impact factor: 3.791

7.  A novel variant in CDKN1C is associated with intrauterine growth restriction, short stature, and early-adulthood-onset diabetes.

Authors:  Sarah L Kerns; Jaime Guevara-Aguirre; Shayne Andrew; Juan Geng; Carolina Guevara; Marco Guevara-Aguirre; Michael Guo; Carole Oddoux; Yiping Shen; Andres Zurita; Ron G Rosenfeld; Harry Ostrer; Vivian Hwa; Andrew Dauber
Journal:  J Clin Endocrinol Metab       Date:  2014-07-24       Impact factor: 5.958

Review 8.  Oncogenic potential of yin yang 1 mediated through control of imprinted genes.

Authors:  Michelle M Thiaville; Joomyeong Kim
Journal:  Crit Rev Oncog       Date:  2011

Review 9.  Beckwith-Wiedemann syndrome and the insulin-like growth factor-II gene. Does the genotype explain the phenotype?

Authors:  D P Witte; K E Bove
Journal:  Am J Pathol       Date:  1994-10       Impact factor: 4.307

10.  Phylogenetic footprint analysis of IGF2 in extant mammals.

Authors:  Jennifer R Weidman; Susan K Murphy; Catherine M Nolan; Fred S Dietrich; Randy L Jirtle
Journal:  Genome Res       Date:  2004-09       Impact factor: 9.043

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