Differential Regulation of PIWI-LIKE 2 Expression in Primordial Germ Cell Tumor Cell Lines by Promoter Methylation
, a member of the ARGONAUTE protein family, is exclusively expressed in pre-pachytene and pachytene stages of spermatogenesis. acts in the germ cell development and the silencing of retrotransponsons to maintain the genomic integrity and stem cell character. In the present study we investigated DNA...
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Published in | Frontiers in genetics Vol. 9; p. 375 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
20.09.2018
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Subjects | |
Online Access | Get full text |
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Summary: | , a member of the ARGONAUTE protein family, is exclusively expressed in pre-pachytene and pachytene stages of spermatogenesis.
acts in the germ cell development and the silencing of retrotransponsons to maintain the genomic integrity and stem cell character. In the present study we investigated DNA methylation as potential mechanism for the regulation of human
expression in cell lines related to spermatozoa precursor cells. We detected a high methylation of the
promoter in TCam-2 cells, while in NT2/D1 cells the promoter was hypomethylated. Concordantly,
expression is higher in NT2/D1 cells than in TCam-2 cells. By demethylation of the promoter with 5'-Aza-2'-deoxycytidine,
expression in TCam-2 was increased, while in NT2/D1 no alterations in
expression could be detected. In conclusion, we analyzed the DNA methylation driving
expression in undifferentiated germ cell tumors and demonstrated an epigenetic basis for
expression in this cell type. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Rui Henrique, IPO Porto, Portugal Reviewed by: Alexandra M. Lopes, Universidade do Porto, Portugal; Michael W. Y. Chan, National Chung Cheng University, Taiwan These authors have contributed equally to this work This article was submitted to Epigenomics and Epigenetics, a section of the journal Frontiers in Genetics |
ISSN: | 1664-8021 1664-8021 |
DOI: | 10.3389/fgene.2018.00375 |