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Nlrp2, a Maternal Effect Gene Required for Early Embryonic Development in the Mouse
Maternal effect genes encode proteins that are produced during oogenesis and play an essential role during early embryogenesis. Genetic ablation of such genes in oocytes can result in female subfertility or infertility. Here we report a newly identified maternal effect gene, Nlrp2, which plays a rol...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266252/ https://www.ncbi.nlm.nih.gov/pubmed/22295082 http://dx.doi.org/10.1371/journal.pone.0030344 |
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author | Peng, Hui Chang, Bohao Lu, Chenglong Su, Jianmin Wu, Yongyan Lv, Pin Wang, Yongsheng Liu, Jun Zhang, Bowei Quan, Fusheng Guo, Zekun Zhang, Yong |
author_facet | Peng, Hui Chang, Bohao Lu, Chenglong Su, Jianmin Wu, Yongyan Lv, Pin Wang, Yongsheng Liu, Jun Zhang, Bowei Quan, Fusheng Guo, Zekun Zhang, Yong |
author_sort | Peng, Hui |
collection | PubMed |
description | Maternal effect genes encode proteins that are produced during oogenesis and play an essential role during early embryogenesis. Genetic ablation of such genes in oocytes can result in female subfertility or infertility. Here we report a newly identified maternal effect gene, Nlrp2, which plays a role in early embryogenesis in the mouse. Nlrp2 mRNAs and their proteins (∼118 KDa) are expressed in oocytes and granulosa cells during folliculogenesis. The transcripts show a striking decline in early preimplantation embryos before zygotic genome activation, but the proteins remain present through to the blastocyst stage. Immunogold electron microscopy revealed that the NLRP2 protein is located in the cytoplasm, nucleus and close to nuclear pores in the oocytes, as well as in the surrounding granulosa cells. Using RNA interference, we knocked down Nlrp2 transcription specifically in mouse germinal vesicle oocytes. The knockdown oocytes could progress through the metaphase of meiosis I and emit the first polar body. However, the development of parthenogenetic embryos derived from Nlrp2 knockdown oocytes mainly blocked at the 2-cell stage. The maternal depletion of Nlrp2 in zygotes led to early embryonic arrest. In addition, overexpression of Nlrp2 in zygotes appears to lead to normal development, but increases blastomere apoptosis in blastocysts. These results provide the first evidence that Nlrp2 is a member of the mammalian maternal effect genes and required for early embryonic development in the mouse. |
format | Online Article Text |
id | pubmed-3266252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32662522012-01-31 Nlrp2, a Maternal Effect Gene Required for Early Embryonic Development in the Mouse Peng, Hui Chang, Bohao Lu, Chenglong Su, Jianmin Wu, Yongyan Lv, Pin Wang, Yongsheng Liu, Jun Zhang, Bowei Quan, Fusheng Guo, Zekun Zhang, Yong PLoS One Research Article Maternal effect genes encode proteins that are produced during oogenesis and play an essential role during early embryogenesis. Genetic ablation of such genes in oocytes can result in female subfertility or infertility. Here we report a newly identified maternal effect gene, Nlrp2, which plays a role in early embryogenesis in the mouse. Nlrp2 mRNAs and their proteins (∼118 KDa) are expressed in oocytes and granulosa cells during folliculogenesis. The transcripts show a striking decline in early preimplantation embryos before zygotic genome activation, but the proteins remain present through to the blastocyst stage. Immunogold electron microscopy revealed that the NLRP2 protein is located in the cytoplasm, nucleus and close to nuclear pores in the oocytes, as well as in the surrounding granulosa cells. Using RNA interference, we knocked down Nlrp2 transcription specifically in mouse germinal vesicle oocytes. The knockdown oocytes could progress through the metaphase of meiosis I and emit the first polar body. However, the development of parthenogenetic embryos derived from Nlrp2 knockdown oocytes mainly blocked at the 2-cell stage. The maternal depletion of Nlrp2 in zygotes led to early embryonic arrest. In addition, overexpression of Nlrp2 in zygotes appears to lead to normal development, but increases blastomere apoptosis in blastocysts. These results provide the first evidence that Nlrp2 is a member of the mammalian maternal effect genes and required for early embryonic development in the mouse. Public Library of Science 2012-01-25 /pmc/articles/PMC3266252/ /pubmed/22295082 http://dx.doi.org/10.1371/journal.pone.0030344 Text en Peng et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Peng, Hui Chang, Bohao Lu, Chenglong Su, Jianmin Wu, Yongyan Lv, Pin Wang, Yongsheng Liu, Jun Zhang, Bowei Quan, Fusheng Guo, Zekun Zhang, Yong Nlrp2, a Maternal Effect Gene Required for Early Embryonic Development in the Mouse |
title |
Nlrp2, a Maternal Effect Gene Required for Early Embryonic Development in the Mouse |
title_full |
Nlrp2, a Maternal Effect Gene Required for Early Embryonic Development in the Mouse |
title_fullStr |
Nlrp2, a Maternal Effect Gene Required for Early Embryonic Development in the Mouse |
title_full_unstemmed |
Nlrp2, a Maternal Effect Gene Required for Early Embryonic Development in the Mouse |
title_short |
Nlrp2, a Maternal Effect Gene Required for Early Embryonic Development in the Mouse |
title_sort | nlrp2, a maternal effect gene required for early embryonic development in the mouse |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266252/ https://www.ncbi.nlm.nih.gov/pubmed/22295082 http://dx.doi.org/10.1371/journal.pone.0030344 |
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