Literature DB >> 19471314

Expression of SNURF-SNRPN upstream transcripts and epigenetic regulatory genes during human spermatogenesis.

Michaela Wawrzik1, Andrej-Nikolai Spiess, Ralf Herrmann, Karin Buiting, Bernhard Horsthemke.   

Abstract

The imprinted domain in human 15q11-q13 is controlled by a bipartite imprinting centre (IC), which overlaps the 5' part of the paternally expressed SNURF-SNRPN gene. We have recently described two novel genes upstream of SNURF-SNRPN (PWRN1 and PWRN2), which are biallelically expressed in the testis. We have now found that PWRN1 represents an alternative 5' part of SNURF-SNRPN, and that its expression in the brain is imprinted. To determine when the locus is activated during spermatogenesis and which factors are involved in this process, we have mined gene-expression data of testicular biopsies from men with different types of spermatogenic failure. Whereas PWRN1-SNURF-SNRPN and PWRN2 are expressed in post-meiotic germ cells only, a hitherto undetected SNURF-SNRPN upstream transcript is expressed already at meiosis. Several epigenetic factors (eg, MBD1 and MBD2 isoforms, MBD3L1, SUVH39H2, BRDT, and EZH2) are upregulated at specific stages of spermatogenesis, suggesting that they play an important role in the epigenetic reprogramming during spermatogenesis.

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Year:  2009        PMID: 19471314      PMCID: PMC2986690          DOI: 10.1038/ejhg.2009.83

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


  20 in total

1.  A new paradigm for profiling testicular gene expression during normal and disturbed human spermatogenesis.

Authors:  C Feig; C Kirchhoff; R Ivell; O Naether; W Schulze; A-N Spiess
Journal:  Mol Hum Reprod       Date:  2006-11-17       Impact factor: 4.025

2.  The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion.

Authors:  C Färber; B Dittrich; K Buiting; B Horsthemke
Journal:  Hum Mol Genet       Date:  1999-02       Impact factor: 6.150

3.  A mammalian protein with specific demethylase activity for mCpG DNA.

Authors:  S K Bhattacharya; S Ramchandani; N Cervoni; M Szyf
Journal:  Nature       Date:  1999-02-18       Impact factor: 49.962

4.  Expression of the Snurf-Snrpn IC transcript in the oocyte and its putative role in the imprinting establishment of the mouse 7C imprinting domain.

Authors:  Christophe K Mapendano; Tatsuya Kishino; Kazumi Miyazaki; Shinji Kondo; Koh-Ichiro Yoshiura; Yoshitaka Hishikawa; Takehiko Koji; Norio Niikawa; Tohru Ohta
Journal:  J Hum Genet       Date:  2006-01-21       Impact factor: 3.172

5.  MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase complex.

Authors:  H H Ng; Y Zhang; B Hendrich; C A Johnson; B M Turner; H Erdjument-Bromage; P Tempst; D Reinberg; A Bird
Journal:  Nat Genet       Date:  1999-09       Impact factor: 38.330

6.  C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brain.

Authors:  Karin Buiting; Hülya Nazlican; Danuta Galetzka; Michaela Wawrzik; Stephanie Gross; Bernhard Horsthemke
Journal:  Genomics       Date:  2007-03-06       Impact factor: 5.736

7.  Identification of unique, differentiation stage-specific patterns of expression of the bromodomain-containing genes Brd2, Brd3, Brd4, and Brdt in the mouse testis.

Authors:  Enyuan Shang; Glicella Salazar; Thomas E Crowley; Xiang Wang; Rocio A Lopez; Xiangyuan Wang; Debra J Wolgemuth
Journal:  Gene Expr Patterns       Date:  2004-09       Impact factor: 1.224

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Authors:  B Hendrich; A Bird
Journal:  Mol Cell Biol       Date:  1998-11       Impact factor: 4.272

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  12 in total

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2.  Copy number variations at the Prader-Willi syndrome region on chromosome 15 and associations with obesity in whites.

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3.  The C15orf2 gene in the Prader-Willi syndrome region is subject to genomic imprinting and positive selection.

Authors:  Michaela Wawrzik; Unga Arifa Unmehopa; Dick Frans Swaab; Johannes van de Nes; Karin Buiting; Bernhard Horsthemke
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4.  Angelman syndrome imprinting center encodes a transcriptional promoter.

Authors:  Michael W Lewis; Jason O Brant; Joseph M Kramer; James I Moss; Thomas P Yang; Peter J Hansen; R Stan Williams; James L Resnick
Journal:  Proc Natl Acad Sci U S A       Date:  2014-11-05       Impact factor: 11.205

5.  Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

Authors:  Merlin G Butler
Journal:  Curr Genomics       Date:  2011-05       Impact factor: 2.236

6.  Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus.

Authors:  Emily Y Smith; Christopher R Futtner; Stormy J Chamberlain; Karen A Johnstone; James L Resnick
Journal:  PLoS Genet       Date:  2011-12-29       Impact factor: 5.917

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9.  Systematic identification of genes with a cancer-testis expression pattern in 19 cancer types.

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10.  Construction and analysis of a lncRNA (PWRN2)-mediated ceRNA network reveal its potential roles in oocyte nuclear maturation of patients with PCOS.

Authors:  Xin Huang; Jiaping Pan; Bi Wu; Xiaoming Teng
Journal:  Reprod Biol Endocrinol       Date:  2018-08-03       Impact factor: 5.211

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