File Download
  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Emi2 Is Essential for Mouse Spermatogenesis

TitleEmi2 Is Essential for Mouse Spermatogenesis
Authors
Keywordsphosphorylation
meiosis
knockout mice
Emi2
diplotene
Cdk1
APC/C
spermatogenesis
spermatocytes
ovary
Issue Date2017
Citation
Cell Reports, 2017, v. 20, n. 3, p. 697-708 How to Cite?
Abstract© 2017 The Author(s) The meiotic functions of Emi2, an inhibitor of the APC/C complex, have been best characterized in oocytes where it mediates metaphase II arrest as a component of the cytostatic factor. We generated knockout mice to determine the in vivo functions of Emi2—in particular, its functions in the testis, where Emi2 is expressed at high levels. Male and female Emi2 knockout mice are viable but sterile, indicating that Emi2 is essential for meiosis but dispensable for embryonic development and mitotic cell divisions. We found that, besides regulating cell-cycle arrest in mouse eggs, Emi2 is essential for meiosis I progression in spermatocytes. In the absence of Emi2, spermatocytes arrest in early diplotene of prophase I. This arrest is associated with decreased Cdk1 activity and was partially rescued by a knockin mouse model of elevated Cdk1 activity. Additionally, we detected expression of Emi2 in spermatids and sperm, suggesting potential post-meiotic functions for Emi2.
Persistent Identifierhttp://hdl.handle.net/10722/265710
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorGopinathan, Lakshmi-
dc.contributor.authorSzmyd, Radoslaw-
dc.contributor.authorLow, Diana-
dc.contributor.authorDiril, M. Kasim-
dc.contributor.authorChang, Heng Yu-
dc.contributor.authorCoppola, Vincenzo-
dc.contributor.authorLiu, Kui-
dc.contributor.authorTessarollo, Lino-
dc.contributor.authorGuccione, Ernesto-
dc.contributor.authorvan Pelt, Ans M.M.-
dc.contributor.authorKaldis, Philipp-
dc.date.accessioned2018-12-03T01:21:28Z-
dc.date.available2018-12-03T01:21:28Z-
dc.date.issued2017-
dc.identifier.citationCell Reports, 2017, v. 20, n. 3, p. 697-708-
dc.identifier.urihttp://hdl.handle.net/10722/265710-
dc.description.abstract© 2017 The Author(s) The meiotic functions of Emi2, an inhibitor of the APC/C complex, have been best characterized in oocytes where it mediates metaphase II arrest as a component of the cytostatic factor. We generated knockout mice to determine the in vivo functions of Emi2—in particular, its functions in the testis, where Emi2 is expressed at high levels. Male and female Emi2 knockout mice are viable but sterile, indicating that Emi2 is essential for meiosis but dispensable for embryonic development and mitotic cell divisions. We found that, besides regulating cell-cycle arrest in mouse eggs, Emi2 is essential for meiosis I progression in spermatocytes. In the absence of Emi2, spermatocytes arrest in early diplotene of prophase I. This arrest is associated with decreased Cdk1 activity and was partially rescued by a knockin mouse model of elevated Cdk1 activity. Additionally, we detected expression of Emi2 in spermatids and sperm, suggesting potential post-meiotic functions for Emi2.-
dc.languageeng-
dc.relation.ispartofCell Reports-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectphosphorylation-
dc.subjectmeiosis-
dc.subjectknockout mice-
dc.subjectEmi2-
dc.subjectdiplotene-
dc.subjectCdk1-
dc.subjectAPC/C-
dc.subjectspermatogenesis-
dc.subjectspermatocytes-
dc.subjectovary-
dc.titleEmi2 Is Essential for Mouse Spermatogenesis-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1016/j.celrep.2017.06.033-
dc.identifier.pmid28723571-
dc.identifier.scopuseid_2-s2.0-85025091691-
dc.identifier.volume20-
dc.identifier.issue3-
dc.identifier.spage697-
dc.identifier.epage708-
dc.identifier.eissn2211-1247-
dc.identifier.isiWOS:000405690100015-
dc.identifier.issnl2211-1247-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats