Literature DB >> 21373884

DNA methylation assay for X-chromosome inactivation in female human iPS cells.

Lesli A Kiedrowski1, Gordana Raca, Jennifer J Laffin, Benjamin S Nisler, Kimberly Leonhard, Erik McIntire, Karen Dyer Mongomery.   

Abstract

Remarkable interest in the epigenetic status of human induced pluripotent stem (iPS) cells inspired numerous studies of their X-inactivation patterns. However, both the presence and the absence of X-inactivation have been described to date in undifferentiated iPS cells. The reasons for the discordant results between different studies are unclear, and further X-inactivation testing is warranted for all female human iPS cell lines. Some of the inconsistency in the current data most likely results from the use of different X-inactivation assays by different authors. We provide a detailed protocol for a simple, reliable and affordable X-inactivation assay based on promoter methylation and CAG-repeat polymorphism in the human androgen receptor (AR) gene at Xq11.2. This assay is commonly used in clinical genetic laboratories and we propose that it could be ideal for routine assessment and monitoring of the X-inactivation status in female human iPS cell lines.

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Year:  2011        PMID: 21373884     DOI: 10.1007/s12015-011-9238-6

Source DB:  PubMed          Journal:  Stem Cell Rev Rep        ISSN: 2629-3277            Impact factor:   5.739


  16 in total

1.  Female human iPSCs retain an inactive X chromosome.

Authors:  Jason Tchieu; Edward Kuoy; Mark H Chin; Hung Trinh; Michaela Patterson; Sean P Sherman; Otaren Aimiuwu; Anne Lindgren; Shahrad Hakimian; Jerome A Zack; Amander T Clark; April D Pyle; William E Lowry; Kathrin Plath
Journal:  Cell Stem Cell       Date:  2010-08-19       Impact factor: 24.633

2.  X-chromosome inactivation and epigenetic fluidity in human embryonic stem cells.

Authors:  Susana S Silva; Rebecca K Rowntree; Shila Mekhoubad; Jeannie T Lee
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-13       Impact factor: 11.205

3.  Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups.

Authors:  A Edwards; H A Hammond; L Jin; C T Caskey; R Chakraborty
Journal:  Genomics       Date:  1992-02       Impact factor: 5.736

4.  Derivation of pre-X inactivation human embryonic stem cells under physiological oxygen concentrations.

Authors:  Christopher J Lengner; Alexander A Gimelbrant; Jennifer A Erwin; Albert Wu Cheng; Matthew G Guenther; G Grant Welstead; Raaji Alagappan; Garrett M Frampton; Ping Xu; Julien Muffat; Sandro Santagata; Doug Powers; C Brent Barrett; Richard A Young; Jeannie T Lee; Rudolf Jaenisch; Maisam Mitalipova
Journal:  Cell       Date:  2010-05-13       Impact factor: 41.582

5.  Directly reprogrammed fibroblasts show global epigenetic remodeling and widespread tissue contribution.

Authors:  Nimet Maherali; Rupa Sridharan; Wei Xie; Jochen Utikal; Sarah Eminli; Katrin Arnold; Matthias Stadtfeld; Robin Yachechko; Jason Tchieu; Rudolf Jaenisch; Kathrin Plath; Konrad Hochedlinger
Journal:  Cell Stem Cell       Date:  2007-06-07       Impact factor: 24.633

6.  Brief report: non-random X chromosome inactivation in females with autism.

Authors:  Z Talebizadeh; D C Bittel; O J Veatch; N Kibiryeva; M G Butler
Journal:  J Autism Dev Disord       Date:  2005-10

7.  X-inactivation reveals epigenetic anomalies in most hESC but identifies sublines that initiate as expected.

Authors:  Lisa L Hall; Meg Byron; John Butler; Klaus A Becker; Angel Nelson; Michal Amit; Joseph Itskovitz-Eldor; Janet Stein; Gary Stein; Carol Ware; Jeanne B Lawrence
Journal:  J Cell Physiol       Date:  2008-08       Impact factor: 6.384

8.  Variations of X chromosome inactivation occur in early passages of female human embryonic stem cells.

Authors:  Tamar Dvash; Neta Lavon; Guoping Fan
Journal:  PLoS One       Date:  2010-06-25       Impact factor: 3.240

9.  Detection of nonrandom X chromosome inactivation.

Authors:  Melissa M Thouin; James M Giron; Eric P Hoffman
Journal:  Curr Protoc Hum Genet       Date:  2003-02

10.  Molecular analysis of Fragile X syndrome.

Authors:  Monica J Basehore; Michael J Friez
Journal:  Curr Protoc Hum Genet       Date:  2009-10
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  6 in total

Review 1.  Inducing iPSCs to escape the dish.

Authors:  Bonnie Barrilleaux; Paul S Knoepfler
Journal:  Cell Stem Cell       Date:  2011-08-05       Impact factor: 24.633

2.  Copy number variation analysis in 83 children with early-onset developmental and epileptic encephalopathy after targeted resequencing of a 109-epilepsy gene panel.

Authors:  Kyoko Hirabayashi; Daniela Tiaki Uehara; Hidetoshi Abe; Atsushi Ishii; Keiji Moriyama; Shinichi Hirose; Johji Inazawa
Journal:  J Hum Genet       Date:  2019-08-30       Impact factor: 3.172

3.  FMR1 epigenetic silencing commonly occurs in undifferentiated fragile X-affected embryonic stem cells.

Authors:  Michal Avitzour; Hagar Mor-Shaked; Shira Yanovsky-Dagan; Shira Aharoni; Gheona Altarescu; Paul Renbaum; Talia Eldar-Geva; Oshrat Schonberger; Ephrat Levy-Lahad; Silvina Epsztejn-Litman; Rachel Eiges
Journal:  Stem Cell Reports       Date:  2014-10-03       Impact factor: 7.765

4.  EPHRIN-B1 Mosaicism Drives Cell Segregation in Craniofrontonasal Syndrome hiPSC-Derived Neuroepithelial Cells.

Authors:  Terren K Niethamer; Andrew R Larson; Audrey K O'Neill; Marina Bershteyn; Edward C Hsiao; Ophir D Klein; Jason H Pomerantz; Jeffrey O Bush
Journal:  Stem Cell Reports       Date:  2017-02-23       Impact factor: 7.765

5.  Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation.

Authors:  David B Beck; Mohammed A Basar; Anthony J Asmar; Joyce J Thompson; Hirotsugu Oda; Daniela T Uehara; Ken Saida; Sander Pajusalu; Inga Talvik; Precilla D'Souza; Joann Bodurtha; Weiyi Mu; Kristin W Barañano; Noriko Miyake; Raymond Wang; Marlies Kempers; Tomoko Tamada; Yutaka Nishimura; Satoshi Okada; Tomoki Kosho; Ryan Dale; Apratim Mitra; Ellen Macnamara; Naomichi Matsumoto; Johji Inazawa; Magdalena Walkiewicz; Katrin Õunap; Cynthia J Tifft; Ivona Aksentijevich; Daniel L Kastner; Pedro P Rocha; Achim Werner
Journal:  Sci Adv       Date:  2021-01-20       Impact factor: 14.136

6.  Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features.

Authors:  Cristiane Benincá; Vanessa Zanette; Michele Brischigliaro; Mark Johnson; Aurelio Reyes; Daniel Almeida do Valle; Alan J Robinson; Andrea Degiorgi; Anna Yeates; Bruno Augusto Telles; Julien Prudent; Enrico Baruffini; Mara Lucia S F Santos; Ricardo Lehtonen R de Souza; Erika Fernandez-Vizarra; Alexander J Whitworth; Massimo Zeviani
Journal:  J Med Genet       Date:  2020-05-21       Impact factor: 6.318

  6 in total

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