Literature DB >> 24823784

Discrimination of pseudogene and parental gene DNA methylation using allelic bisulfite sequencing.

Luke B Hesson1, Robyn L Ward.   

Abstract

Determining the methylation status of genes with pseudogenes can be technically challenging due to sequence homology. High sequence homology can result in the amplification of both pseudogene and parental gene alleles, potentially leading to data misinterpretation. Allelic bisulfite sequencing allows for detection of the methylation status of individual alleles at nucleotide resolution and represents the most reliable method for discriminating pseudogene and parental gene sequences. Here, we discuss important points that should be considered when investigating pseudogene and parental gene methylation status and we describe the method of allelic bisulfite sequencing, including assay design.

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Year:  2014        PMID: 24823784     DOI: 10.1007/978-1-4939-0835-6_18

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  6 in total

1.  Altered promoter nucleosome positioning is an early event in gene silencing.

Authors:  Luke B Hesson; Mathew A Sloane; Jason Wh Wong; Andrea C Nunez; Sameer Srivastava; Benedict Ng; Nicholas J Hawkins; Michael J Bourke; Robyn L Ward
Journal:  Epigenetics       Date:  2014-10       Impact factor: 4.528

2.  The importance of distinguishing pseudogenes from parental genes.

Authors:  Luke B Hesson; Robyn L Ward
Journal:  Clin Epigenetics       Date:  2014-12-31       Impact factor: 6.551

3.  Overexpression of KLHL23 protein from read-through transcription of PHOSPHO2-KLHL23 in gastric cancer increases cell proliferation.

Authors:  Eun-Seok Choi; Hanna Lee; Chang-Hun Lee; Sung-Ho Goh
Journal:  FEBS Open Bio       Date:  2016-10-24       Impact factor: 2.693

Review 4.  Focus on PTEN Regulation.

Authors:  Miriam Bermúdez Brito; Evangelia Goulielmaki; Evangelia A Papakonstanti
Journal:  Front Oncol       Date:  2015-07-27       Impact factor: 6.244

5.  Nucleosome positioning is unaltered at MLH1 splice site mutations in cells derived from Lynch syndrome patients.

Authors:  Mathew A Sloane; Luke B Hesson; Andrea C Nunez; Bryony A Thompson; Robyn L Ward
Journal:  Clin Epigenetics       Date:  2014-12-13       Impact factor: 6.551

6.  Lynch syndrome associated with two MLH1 promoter variants and allelic imbalance of MLH1 expression.

Authors:  Luke B Hesson; Deborah Packham; Chau-To Kwok; Andrea C Nunez; Benedict Ng; Christa Schmidt; Michael Fields; Jason W H Wong; Mathew A Sloane; Robyn L Ward
Journal:  Hum Mutat       Date:  2015-04-17       Impact factor: 4.878

  6 in total

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