File Download
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.celrep.2017.06.033
- Scopus: eid_2-s2.0-85025091691
- PMID: 28723571
- WOS: WOS:000405690100015
Supplementary
- Citations:
- Appears in Collections:
Article: Emi2 Is Essential for Mouse Spermatogenesis
Title | Emi2 Is Essential for Mouse Spermatogenesis |
---|---|
Authors | |
Keywords | phosphorylation meiosis knockout mice Emi2 diplotene Cdk1 APC/C spermatogenesis spermatocytes ovary |
Issue Date | 2017 |
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 Identifier | http://hdl.handle.net/10722/265710 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Gopinathan, Lakshmi | - |
dc.contributor.author | Szmyd, Radoslaw | - |
dc.contributor.author | Low, Diana | - |
dc.contributor.author | Diril, M. Kasim | - |
dc.contributor.author | Chang, Heng Yu | - |
dc.contributor.author | Coppola, Vincenzo | - |
dc.contributor.author | Liu, Kui | - |
dc.contributor.author | Tessarollo, Lino | - |
dc.contributor.author | Guccione, Ernesto | - |
dc.contributor.author | van Pelt, Ans M.M. | - |
dc.contributor.author | Kaldis, Philipp | - |
dc.date.accessioned | 2018-12-03T01:21:28Z | - |
dc.date.available | 2018-12-03T01:21:28Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Cell Reports, 2017, v. 20, n. 3, p. 697-708 | - |
dc.identifier.uri | http://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.language | eng | - |
dc.relation.ispartof | Cell Reports | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | phosphorylation | - |
dc.subject | meiosis | - |
dc.subject | knockout mice | - |
dc.subject | Emi2 | - |
dc.subject | diplotene | - |
dc.subject | Cdk1 | - |
dc.subject | APC/C | - |
dc.subject | spermatogenesis | - |
dc.subject | spermatocytes | - |
dc.subject | ovary | - |
dc.title | Emi2 Is Essential for Mouse Spermatogenesis | - |
dc.type | Article | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1016/j.celrep.2017.06.033 | - |
dc.identifier.pmid | 28723571 | - |
dc.identifier.scopus | eid_2-s2.0-85025091691 | - |
dc.identifier.volume | 20 | - |
dc.identifier.issue | 3 | - |
dc.identifier.spage | 697 | - |
dc.identifier.epage | 708 | - |
dc.identifier.eissn | 2211-1247 | - |
dc.identifier.isi | WOS:000405690100015 | - |
dc.identifier.issnl | 2211-1247 | - |