Literature DB >> 34037318

Phenotypically concordant but epigenetically discordant monozygotic dichorionic diamniotic twins with Beckwith-Wiedemann syndrome.

Feifei Sun1,2, Satoshi Hara1, Chiyoko Tomita3, Yuka Tanoue1, Hitomi Yatsuki1, Ken Higashimoto1, Hidenobu Soejima1.   

Abstract

Beckwith-Wiedemann syndrome (BWS) is an imprinting disorder caused by (epi)genetic alterations. The incidence of monozygotic (MZ) twins in BWS is higher than in the general population. Most MZ twins with BWS are female and have phenotypical discordance: one twin is clinically diagnosed with BWS, while the other shows a mild or normal phenotype. The most frequent (epi)genetic alteration in MZ twins is loss of methylation of imprinting control region 2 (ICR2-LOM) at 11p15.5. Intriguingly, ICR2-LOM is usually found in the peripheral blood leukocytes (PBL) of both twins, even if they are clinically discordant. Here, we present a rare pair of MZ dichorionic diamniotic female twins with BWS and concordant phenotypes (a Beckwith-Wiedemann spectrum score of 5 in each twin). Molecular analysis of genomic DNA from PBL revealed ICR2-LOM in one twin but not the other. Our analyses suggest that ICR2-LOM occurred between days 1 and 3 after fertilization, followed by twinning. We speculate that during embryogenesis, ICR2-LOM cells were distributed to the hematopoietic stem cells in different ratios in the two fetuses, and also to commonly affected tissues, such as the tongue, in similar ratios, although we were unable to analyze any tissues other than PBL.
© 2021 Wiley Periodicals LLC.

Entities:  

Keywords:  Beckwith-Wiedemann syndrome; dichorionic diamniotic twins; epigenetic mosaicism; loss of methylation; monozygotic twins

Mesh:

Year:  2021        PMID: 34037318     DOI: 10.1002/ajmg.a.62364

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  3 in total

1.  Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia.

Authors:  Saori Aoki; Ken Higashimoto; Hidenori Hidaka; Yasufumi Ohtsuka; Shigehisa Aoki; Hiroyuki Mishima; Koh-Ichiro Yoshiura; Kazuhiko Nakabayashi; Kenichiro Hata; Hitomi Yatsuki; Satoshi Hara; Takashi Ohba; Hidetaka Katabuchi; Hidenobu Soejima
Journal:  Clin Epigenetics       Date:  2022-05-17       Impact factor: 7.259

2.  Characteristics Associated with Tumor Development in Individuals Diagnosed with Beckwith-Wiedemann Spectrum: Novel Tumor-(epi)Genotype-Phenotype Associations in the BWSp Population.

Authors:  Kelly A Duffy; Kelly D Getz; Evan R Hathaway; Mallory E Byrne; Suzanne P MacFarland; Jennifer M Kalish
Journal:  Genes (Basel)       Date:  2021-11-21       Impact factor: 4.096

3.  Epigenetic mosaicism and cell burden in Beckwith-Wiedemann syndrome due to loss of methylation at imprinting control region 2.

Authors:  Kelly A Duffy; Evan R Hathaway; Steven D Klein; Arupa Ganguly; Jennifer M Kalish
Journal:  Cold Spring Harb Mol Case Stud       Date:  2021-12-09
  3 in total

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