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Identification and Epigenetic Analysis of a Maternally Imprinted Gene Qpct
Most imprinted genes are concerned with embryonic development, especially placental development. Here, we identified a placenta-specific imprinted gene Qpct. Our results show that Qpct is widely expressed during early embryonic development and can be detected in the telecephalon, midbrain, and rhomb...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Molecular and Cellular Biology
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625067/ https://www.ncbi.nlm.nih.gov/pubmed/26447138 http://dx.doi.org/10.14348/molcells.2015.0098 |
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author | Guo, Jing He, Hongjuan Liu, Qi Zhang, Fengwei Lv, Jie Zeng, Tiebo Gu, Ning Wu, Qiong |
author_facet | Guo, Jing He, Hongjuan Liu, Qi Zhang, Fengwei Lv, Jie Zeng, Tiebo Gu, Ning Wu, Qiong |
author_sort | Guo, Jing |
collection | PubMed |
description | Most imprinted genes are concerned with embryonic development, especially placental development. Here, we identified a placenta-specific imprinted gene Qpct. Our results show that Qpct is widely expressed during early embryonic development and can be detected in the telecephalon, midbrain, and rhombencephalon at E9.5–E11.5. Moreover, Qpct is strikingly expressed in the brain, lung and liver in E15.5. Expression signals for Qpct achieved a peak at E15.5 during placental development and were only detected in the labyrinth layer in E15.5 placenta. ChIP assay results suggest that the modification of histone H3K4me3 can result in maternal activating of Qpct. |
format | Online Article Text |
id | pubmed-4625067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Korean Society for Molecular and Cellular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-46250672015-11-03 Identification and Epigenetic Analysis of a Maternally Imprinted Gene Qpct Guo, Jing He, Hongjuan Liu, Qi Zhang, Fengwei Lv, Jie Zeng, Tiebo Gu, Ning Wu, Qiong Mol Cells Article Most imprinted genes are concerned with embryonic development, especially placental development. Here, we identified a placenta-specific imprinted gene Qpct. Our results show that Qpct is widely expressed during early embryonic development and can be detected in the telecephalon, midbrain, and rhombencephalon at E9.5–E11.5. Moreover, Qpct is strikingly expressed in the brain, lung and liver in E15.5. Expression signals for Qpct achieved a peak at E15.5 during placental development and were only detected in the labyrinth layer in E15.5 placenta. ChIP assay results suggest that the modification of histone H3K4me3 can result in maternal activating of Qpct. Korean Society for Molecular and Cellular Biology 2015-10-31 2015-10-12 /pmc/articles/PMC4625067/ /pubmed/26447138 http://dx.doi.org/10.14348/molcells.2015.0098 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/. |
spellingShingle | Article Guo, Jing He, Hongjuan Liu, Qi Zhang, Fengwei Lv, Jie Zeng, Tiebo Gu, Ning Wu, Qiong Identification and Epigenetic Analysis of a Maternally Imprinted Gene Qpct |
title | Identification and Epigenetic Analysis of a Maternally Imprinted Gene Qpct |
title_full | Identification and Epigenetic Analysis of a Maternally Imprinted Gene Qpct |
title_fullStr | Identification and Epigenetic Analysis of a Maternally Imprinted Gene Qpct |
title_full_unstemmed | Identification and Epigenetic Analysis of a Maternally Imprinted Gene Qpct |
title_short | Identification and Epigenetic Analysis of a Maternally Imprinted Gene Qpct |
title_sort | identification and epigenetic analysis of a maternally imprinted gene qpct |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625067/ https://www.ncbi.nlm.nih.gov/pubmed/26447138 http://dx.doi.org/10.14348/molcells.2015.0098 |
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