Literature DB >> 1534643

Epigene conversion: a proposal with implications for gene mapping in humans.

J F Sabl1, C D Laird.   

Abstract

Epigenetic modification of DNA is now recognized as a potentially important factor in the inheritance and expression of some mutations; its ability to complicate human genetic analysis is concurrently becoming apparent. One unusual form of epigenetic modification, dominant position-effect variegation (PEV), has been used as a model for Huntington disease. In dominant PEV, a fully dominant mutant phenotype results from stable epigenetic inactivation of an allele adjacent to the structural alteration (cis-inactivation) combined with a complementary inactivation of the homologous normal allele (trans-inactivation). We now propose that trans-inactivation of the normal allele may occasionally persist through meiosis. Such "epigene conversion" occurring at the Huntington disease locus in a few percent of meioses would largely account for the published anomalies in that region's genetic map. This concept could also explain anomalous linkage map data for other disease-causing alleles in humans.

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Year:  1992        PMID: 1534643      PMCID: PMC1682548     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  20 in total

1.  ABERRANT RECOMBINATION OF PYRIDOXINE MUTANTS OF Neurospora.

Authors:  M B Mitchell
Journal:  Proc Natl Acad Sci U S A       Date:  1955-04-15       Impact factor: 11.205

2.  The end in sight for Huntington disease?

Authors:  C Pritchard; D R Cox; R M Myers
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

3.  Recombination events suggest potential sites for the Huntington's disease gene.

Authors:  M E MacDonald; J L Haines; M Zimmer; S V Cheng; S Youngman; W L Whaley; N Wexler; M Bucan; B A Allitto; B Smith
Journal:  Neuron       Date:  1989-08       Impact factor: 17.173

4.  How does the cell count the number of ectopic copies of a gene in the premeiotic inactivation process acting in Ascobolus immersus?

Authors:  G Faugeron; L Rhounim; J L Rossignol
Journal:  Genetics       Date:  1990-03       Impact factor: 4.562

Review 5.  Paramutation.

Authors:  R A Brink
Journal:  Annu Rev Genet       Date:  1973       Impact factor: 16.830

6.  Complex patterns of linkage disequilibrium in the Huntington disease region.

Authors:  M E MacDonald; C Lin; L Srinidhi; G Bates; M Altherr; W L Whaley; H Lehrach; J Wasmuth; J F Gusella
Journal:  Am J Hum Genet       Date:  1991-10       Impact factor: 11.025

7.  A polymorphic DNA marker genetically linked to Huntington's disease.

Authors:  J F Gusella; N S Wexler; P M Conneally; S L Naylor; M A Anderson; R E Tanzi; P C Watkins; K Ottina; M R Wallace; A Y Sakaguchi
Journal:  Nature       Date:  1983 Nov 17-23       Impact factor: 49.962

8.  A sequence motif found in a Drosophila heterochromatin protein is conserved in animals and plants.

Authors:  P B Singh; J R Miller; J Pearce; R Kothary; R D Burton; R Paro; T C James; S J Gaunt
Journal:  Nucleic Acids Res       Date:  1991-02-25       Impact factor: 16.971

9.  Homozygotes for Huntington's disease.

Authors:  N S Wexler; A B Young; R E Tanzi; H Travers; S Starosta-Rubinstein; J B Penney; S R Snodgrass; I Shoulson; F Gomez; M A Ramos Arroyo
Journal:  Nature       Date:  1987 Mar 12-18       Impact factor: 49.962

10.  Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.

Authors:  C Robbins; J Theilmann; S Youngman; J Haines; M J Altherr; P S Harper; C Payne; A Junker; J Wasmuth; M R Hayden
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025

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  8 in total

1.  Effects of chromosomal rearrangements on transvection at the yellow gene of Drosophila melanogaster.

Authors:  Sharon A Ou; Elaine Chang; Szexian Lee; Katherine So; C-ting Wu; James R Morris
Journal:  Genetics       Date:  2009-08-10       Impact factor: 4.562

2.  Paramutation, an allelic interaction, is associated with a stable and heritable reduction of transcription of the maize b regulatory gene.

Authors:  G I Patterson; C J Thorpe; V L Chandler
Journal:  Genetics       Date:  1993-11       Impact factor: 4.562

3.  Position-dependent methylation and transcriptional silencing of transgenes in inverted T-DNA repeats: implications for posttranscriptional silencing of homologous host genes in plants.

Authors:  M Stam; A Viterbo; J N Mol; J M Kooter
Journal:  Mol Cell Biol       Date:  1998-11       Impact factor: 4.272

4.  Homology-dependent gene silencing in transgenic plants: epistatic silencing loci contain multiple copies of methylated transgenes.

Authors:  A J Matzke; F Neuhuber; Y D Park; P F Ambros; M A Matzke
Journal:  Mol Gen Genet       Date:  1994-08-02

5.  Maternal and paternal genomes function independently in mouse ova in establishing expression of the imprinted genes Snrpn and Igf2r: no evidence for allelic trans-sensing and counting mechanisms.

Authors:  P E Szabó; J R Mann
Journal:  EMBO J       Date:  1996-11-15       Impact factor: 11.598

6.  Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q.

Authors:  S G Ryan; M J Dixon; M A Nigro; K A Kelts; O N Markand; J C Terry; R Shiang; J J Wasmuth; P O'Connell
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

Review 7.  The role of genetics in the establishment and maintenance of the epigenome.

Authors:  Covadonga Huidobro; Agustin F Fernandez; Mario F Fraga
Journal:  Cell Mol Life Sci       Date:  2013-03-10       Impact factor: 9.261

Review 8.  Transvection, nuclear structure, and chromatin proteins.

Authors:  C T Wu
Journal:  J Cell Biol       Date:  1993-02       Impact factor: 10.539

  8 in total

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