Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Peng, Hui, Chang, Bohao, Lu, Chenglong, Su, Jianmin, Wu, Yongyan, Lv, Pin, Wang, Yongsheng, Liu, Jun, Zhang, Bowei, Quan, Fusheng, Guo, Zekun, Zhang, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
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
_version_ 1782222155781505024
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
work_keys_str_mv AT penghui nlrp2amaternaleffectgenerequiredforearlyembryonicdevelopmentinthemouse
AT changbohao nlrp2amaternaleffectgenerequiredforearlyembryonicdevelopmentinthemouse
AT luchenglong nlrp2amaternaleffectgenerequiredforearlyembryonicdevelopmentinthemouse
AT sujianmin nlrp2amaternaleffectgenerequiredforearlyembryonicdevelopmentinthemouse
AT wuyongyan nlrp2amaternaleffectgenerequiredforearlyembryonicdevelopmentinthemouse
AT lvpin nlrp2amaternaleffectgenerequiredforearlyembryonicdevelopmentinthemouse
AT wangyongsheng nlrp2amaternaleffectgenerequiredforearlyembryonicdevelopmentinthemouse
AT liujun nlrp2amaternaleffectgenerequiredforearlyembryonicdevelopmentinthemouse
AT zhangbowei nlrp2amaternaleffectgenerequiredforearlyembryonicdevelopmentinthemouse
AT quanfusheng nlrp2amaternaleffectgenerequiredforearlyembryonicdevelopmentinthemouse
AT guozekun nlrp2amaternaleffectgenerequiredforearlyembryonicdevelopmentinthemouse
AT zhangyong nlrp2amaternaleffectgenerequiredforearlyembryonicdevelopmentinthemouse