The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation

Autores
Ball, Christopher B.; Rodriguez, Karina F.; Stumpo, Deborah J.; Ribeiro Neto, Fernando; Korach, Kenneth S.; Blackshear, Perry J.; Birnbaumer, Lutz; Ramos, Silvia B. V.
Año de publicación
2014
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
ZFP36L2 protein destabilizes AU-rich element-containing transcripts and has been implicated in female fertility. In the C57BL/6NTac mouse, a mutation in Zfp36l2 that results in the decreased expression of a form of ZFP36L2 in which the 29 N-terminal amino acid residues have been deleted, ΔN-ZFP36L2, leads to fertilized eggs that arrest at the two-cell stage. Interestingly, homozygous ΔN-Zfp36l2 females in the C57BL/6NTac strain release 40% fewer eggs than the WT littermates (Ramos et al., 2004), suggesting an additional defect in ovulation and/or oocyte maturation. Curiously, the same ΔN-Zfp36l2 mutation into the SV129 strain resulted in anovulation, prompting us to investigate a potential problem in ovulation and oocyte maturation. Remarkably, only 20% of ΔN-Zfp36l2 oocytes in the 129S6/SvEvTac strain matured ex vivo, suggesting a defect on the oocyte meiotic maturation process. Treatment of ΔN-Zfp36l2 oocytes with a PKA inhibitor partially rescued the meiotic arrested oocytes. Furthermore, cAMP levels were increased in ΔN-Zfp36l2 oocytes, linking the cAMP/PKA pathway and ΔN-Zfp36l2 with meiotic arrest. Since ovulation and oocyte maturation are both triggered by LHR signaling, the downstream pathway was investigated. Adenylyl cyclase activity was increased in ΔN-Zfp36l2 ovaries only upon LH stimulation. Moreover, we discovered that ZFP36L2 interacts with the 3′UTR of LHR mRNA and that decreased expression levels of Zfp36l2 correlates with higher levels of LHR mRNA in synchronized ovaries. Furthermore, overexpression of ZFP36L2 decreases the endogenous expression of LHR mRNA in a cell line. Therefore, we propose that lack of the physiological down regulation of LHR mRNA levels by ZFP36L2 in the ovaries is associated with anovulation and oocyte meiotic arrest.
Fil: Ball, Christopher B.. University of North Carolina; Estados Unidos
Fil: Rodriguez, Karina F.. National Institutes of Health; Estados Unidos
Fil: Stumpo, Deborah J.. National Institutes of Health; Estados Unidos
Fil: Ribeiro Neto, Fernando. National Institutes of Health; Estados Unidos
Fil: Korach, Kenneth S.. National Institutes of Health; Estados Unidos
Fil: Blackshear, Perry J.. University of Duke; Estados Unidos. National Institutes of Health; Estados Unidos
Fil: Birnbaumer, Lutz. National Institutes of Health; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Ramos, Silvia B. V.. University of North Carolina; Estados Unidos
Materia
ZFP36L2
Oocyte Maturation
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/96256

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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturationBall, Christopher B.Rodriguez, Karina F.Stumpo, Deborah J.Ribeiro Neto, FernandoKorach, Kenneth S.Blackshear, Perry J.Birnbaumer, LutzRamos, Silvia B. V.ZFP36L2Oocyte Maturationhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1ZFP36L2 protein destabilizes AU-rich element-containing transcripts and has been implicated in female fertility. In the C57BL/6NTac mouse, a mutation in Zfp36l2 that results in the decreased expression of a form of ZFP36L2 in which the 29 N-terminal amino acid residues have been deleted, ΔN-ZFP36L2, leads to fertilized eggs that arrest at the two-cell stage. Interestingly, homozygous ΔN-Zfp36l2 females in the C57BL/6NTac strain release 40% fewer eggs than the WT littermates (Ramos et al., 2004), suggesting an additional defect in ovulation and/or oocyte maturation. Curiously, the same ΔN-Zfp36l2 mutation into the SV129 strain resulted in anovulation, prompting us to investigate a potential problem in ovulation and oocyte maturation. Remarkably, only 20% of ΔN-Zfp36l2 oocytes in the 129S6/SvEvTac strain matured ex vivo, suggesting a defect on the oocyte meiotic maturation process. Treatment of ΔN-Zfp36l2 oocytes with a PKA inhibitor partially rescued the meiotic arrested oocytes. Furthermore, cAMP levels were increased in ΔN-Zfp36l2 oocytes, linking the cAMP/PKA pathway and ΔN-Zfp36l2 with meiotic arrest. Since ovulation and oocyte maturation are both triggered by LHR signaling, the downstream pathway was investigated. Adenylyl cyclase activity was increased in ΔN-Zfp36l2 ovaries only upon LH stimulation. Moreover, we discovered that ZFP36L2 interacts with the 3′UTR of LHR mRNA and that decreased expression levels of Zfp36l2 correlates with higher levels of LHR mRNA in synchronized ovaries. Furthermore, overexpression of ZFP36L2 decreases the endogenous expression of LHR mRNA in a cell line. Therefore, we propose that lack of the physiological down regulation of LHR mRNA levels by ZFP36L2 in the ovaries is associated with anovulation and oocyte meiotic arrest.Fil: Ball, Christopher B.. University of North Carolina; Estados UnidosFil: Rodriguez, Karina F.. National Institutes of Health; Estados UnidosFil: Stumpo, Deborah J.. National Institutes of Health; Estados UnidosFil: Ribeiro Neto, Fernando. National Institutes of Health; Estados UnidosFil: Korach, Kenneth S.. National Institutes of Health; Estados UnidosFil: Blackshear, Perry J.. University of Duke; Estados Unidos. National Institutes of Health; Estados UnidosFil: Birnbaumer, Lutz. National Institutes of Health; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Ramos, Silvia B. V.. University of North Carolina; Estados UnidosPublic Library of Science2014-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/96256Ball, Christopher B.; Rodriguez, Karina F.; Stumpo, Deborah J.; Ribeiro Neto, Fernando; Korach, Kenneth S.; et al.; The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation; Public Library of Science; Plos One; 9; 5; 5-2014; 1-121932-6203CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0097324info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0097324info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:16:06Zoai:ri.conicet.gov.ar:11336/96256instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-10 13:16:07.034CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation
title The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation
spellingShingle The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation
Ball, Christopher B.
ZFP36L2
Oocyte Maturation
title_short The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation
title_full The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation
title_fullStr The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation
title_full_unstemmed The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation
title_sort The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation
dc.creator.none.fl_str_mv Ball, Christopher B.
Rodriguez, Karina F.
Stumpo, Deborah J.
Ribeiro Neto, Fernando
Korach, Kenneth S.
Blackshear, Perry J.
Birnbaumer, Lutz
Ramos, Silvia B. V.
author Ball, Christopher B.
author_facet Ball, Christopher B.
Rodriguez, Karina F.
Stumpo, Deborah J.
Ribeiro Neto, Fernando
Korach, Kenneth S.
Blackshear, Perry J.
Birnbaumer, Lutz
Ramos, Silvia B. V.
author_role author
author2 Rodriguez, Karina F.
Stumpo, Deborah J.
Ribeiro Neto, Fernando
Korach, Kenneth S.
Blackshear, Perry J.
Birnbaumer, Lutz
Ramos, Silvia B. V.
author2_role author
author
author
author
author
author
author
dc.subject.none.fl_str_mv ZFP36L2
Oocyte Maturation
topic ZFP36L2
Oocyte Maturation
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv ZFP36L2 protein destabilizes AU-rich element-containing transcripts and has been implicated in female fertility. In the C57BL/6NTac mouse, a mutation in Zfp36l2 that results in the decreased expression of a form of ZFP36L2 in which the 29 N-terminal amino acid residues have been deleted, ΔN-ZFP36L2, leads to fertilized eggs that arrest at the two-cell stage. Interestingly, homozygous ΔN-Zfp36l2 females in the C57BL/6NTac strain release 40% fewer eggs than the WT littermates (Ramos et al., 2004), suggesting an additional defect in ovulation and/or oocyte maturation. Curiously, the same ΔN-Zfp36l2 mutation into the SV129 strain resulted in anovulation, prompting us to investigate a potential problem in ovulation and oocyte maturation. Remarkably, only 20% of ΔN-Zfp36l2 oocytes in the 129S6/SvEvTac strain matured ex vivo, suggesting a defect on the oocyte meiotic maturation process. Treatment of ΔN-Zfp36l2 oocytes with a PKA inhibitor partially rescued the meiotic arrested oocytes. Furthermore, cAMP levels were increased in ΔN-Zfp36l2 oocytes, linking the cAMP/PKA pathway and ΔN-Zfp36l2 with meiotic arrest. Since ovulation and oocyte maturation are both triggered by LHR signaling, the downstream pathway was investigated. Adenylyl cyclase activity was increased in ΔN-Zfp36l2 ovaries only upon LH stimulation. Moreover, we discovered that ZFP36L2 interacts with the 3′UTR of LHR mRNA and that decreased expression levels of Zfp36l2 correlates with higher levels of LHR mRNA in synchronized ovaries. Furthermore, overexpression of ZFP36L2 decreases the endogenous expression of LHR mRNA in a cell line. Therefore, we propose that lack of the physiological down regulation of LHR mRNA levels by ZFP36L2 in the ovaries is associated with anovulation and oocyte meiotic arrest.
Fil: Ball, Christopher B.. University of North Carolina; Estados Unidos
Fil: Rodriguez, Karina F.. National Institutes of Health; Estados Unidos
Fil: Stumpo, Deborah J.. National Institutes of Health; Estados Unidos
Fil: Ribeiro Neto, Fernando. National Institutes of Health; Estados Unidos
Fil: Korach, Kenneth S.. National Institutes of Health; Estados Unidos
Fil: Blackshear, Perry J.. University of Duke; Estados Unidos. National Institutes of Health; Estados Unidos
Fil: Birnbaumer, Lutz. National Institutes of Health; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Ramos, Silvia B. V.. University of North Carolina; Estados Unidos
description ZFP36L2 protein destabilizes AU-rich element-containing transcripts and has been implicated in female fertility. In the C57BL/6NTac mouse, a mutation in Zfp36l2 that results in the decreased expression of a form of ZFP36L2 in which the 29 N-terminal amino acid residues have been deleted, ΔN-ZFP36L2, leads to fertilized eggs that arrest at the two-cell stage. Interestingly, homozygous ΔN-Zfp36l2 females in the C57BL/6NTac strain release 40% fewer eggs than the WT littermates (Ramos et al., 2004), suggesting an additional defect in ovulation and/or oocyte maturation. Curiously, the same ΔN-Zfp36l2 mutation into the SV129 strain resulted in anovulation, prompting us to investigate a potential problem in ovulation and oocyte maturation. Remarkably, only 20% of ΔN-Zfp36l2 oocytes in the 129S6/SvEvTac strain matured ex vivo, suggesting a defect on the oocyte meiotic maturation process. Treatment of ΔN-Zfp36l2 oocytes with a PKA inhibitor partially rescued the meiotic arrested oocytes. Furthermore, cAMP levels were increased in ΔN-Zfp36l2 oocytes, linking the cAMP/PKA pathway and ΔN-Zfp36l2 with meiotic arrest. Since ovulation and oocyte maturation are both triggered by LHR signaling, the downstream pathway was investigated. Adenylyl cyclase activity was increased in ΔN-Zfp36l2 ovaries only upon LH stimulation. Moreover, we discovered that ZFP36L2 interacts with the 3′UTR of LHR mRNA and that decreased expression levels of Zfp36l2 correlates with higher levels of LHR mRNA in synchronized ovaries. Furthermore, overexpression of ZFP36L2 decreases the endogenous expression of LHR mRNA in a cell line. Therefore, we propose that lack of the physiological down regulation of LHR mRNA levels by ZFP36L2 in the ovaries is associated with anovulation and oocyte meiotic arrest.
publishDate 2014
dc.date.none.fl_str_mv 2014-05
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/96256
Ball, Christopher B.; Rodriguez, Karina F.; Stumpo, Deborah J.; Ribeiro Neto, Fernando; Korach, Kenneth S.; et al.; The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation; Public Library of Science; Plos One; 9; 5; 5-2014; 1-12
1932-6203
CONICET Digital
CONICET
url http://hdl.handle.net/11336/96256
identifier_str_mv Ball, Christopher B.; Rodriguez, Karina F.; Stumpo, Deborah J.; Ribeiro Neto, Fernando; Korach, Kenneth S.; et al.; The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation; Public Library of Science; Plos One; 9; 5; 5-2014; 1-12
1932-6203
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0097324
info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0097324
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Public Library of Science
publisher.none.fl_str_mv Public Library of Science
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
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repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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