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The APC activator fizzy-related-1 (FZR1) is needed for preimplantation mouse embryo development

The APC activator fizzy-related-1 (FZR1) is needed for preimplantation mouse embryo development
The APC activator fizzy-related-1 (FZR1) is needed for preimplantation mouse embryo development
In early embryos of a number of species the anaphase-promoting complex (APC), an important cell cycle regulator, requires only CDC20 for cell division. In contrast, fizzy-related-1 (FZR1), a non-essential protein in many cell types, is thought to play a role in APC activation at later cell cycles, and especially in endoreduplication. In keeping with this, Fzr1 knockout mouse embryos show normal preimplantation development but die due to a lack of endoreduplication needed for placentation. However, interpretation of the role of FZR1 during this period is hindered by the presence of maternal stores. In this study, therefore, we used an oocyte-specific knockout to examine FZR1 function in early mouse embryo development. Maternal FZR1 was not crucial for completion of meiosis, and furthermore viable pups were born to Fzr1 knockout females mated with normal males. However, in early embryos the absence of both maternal and paternal FZR1 led to a dramatic loss in genome integrity, such that the majority of embryos arrested having undergone only a single mitotic division and contained many ?-H2AX foci, consistent with fragmented DNA. A prominent feature of such embryos was the establishment of two independent spindles following pronuclear fusion and thus a failure of the chromosomes to mix (syngamy). These generated binucleate 2-cell embryos. In the 10% of embryos that progressed to the 4-cell stage, division was so slow that compaction occurred prematurely. No embryo development to the blastocyst stage was ever observed. We conclude that Fzr1 is a surprisingly essential gene involved in the establishment of a single spindle from the two pronuclei in 1-cell embryos as well as being involved in the maintenance of genomic integrity during the mitotic divisions of early mammalian embryos.
mammalian embryos, meiosis, oocytes, mitosis, syngamy compaction
0021-9533
6030-6037
Seah, MKY
b9c5ffd0-7d14-4c3c-969c-cecfbad2cc93
Holt, JE
c2b8b241-75af-4c44-972b-af9508fcfc2a
García-Higuera, I
a624ede1-2ccb-4256-a4cc-f068a51a1d0f
Moreno, S
3b8cac11-c963-4222-befd-162ee0587ac2
Jones, KT
73e8e2b5-cd67-4691-b1a9-4e7bc9066af4
Seah, MKY
b9c5ffd0-7d14-4c3c-969c-cecfbad2cc93
Holt, JE
c2b8b241-75af-4c44-972b-af9508fcfc2a
García-Higuera, I
a624ede1-2ccb-4256-a4cc-f068a51a1d0f
Moreno, S
3b8cac11-c963-4222-befd-162ee0587ac2
Jones, KT
73e8e2b5-cd67-4691-b1a9-4e7bc9066af4

Seah, MKY, Holt, JE, García-Higuera, I, Moreno, S and Jones, KT (2012) The APC activator fizzy-related-1 (FZR1) is needed for preimplantation mouse embryo development. Journal of Cell Science, 125 (Pt24), 6030-6037. (doi:10.1242/?jcs.110155). (PMID:23097041)

Record type: Article

Abstract

In early embryos of a number of species the anaphase-promoting complex (APC), an important cell cycle regulator, requires only CDC20 for cell division. In contrast, fizzy-related-1 (FZR1), a non-essential protein in many cell types, is thought to play a role in APC activation at later cell cycles, and especially in endoreduplication. In keeping with this, Fzr1 knockout mouse embryos show normal preimplantation development but die due to a lack of endoreduplication needed for placentation. However, interpretation of the role of FZR1 during this period is hindered by the presence of maternal stores. In this study, therefore, we used an oocyte-specific knockout to examine FZR1 function in early mouse embryo development. Maternal FZR1 was not crucial for completion of meiosis, and furthermore viable pups were born to Fzr1 knockout females mated with normal males. However, in early embryos the absence of both maternal and paternal FZR1 led to a dramatic loss in genome integrity, such that the majority of embryos arrested having undergone only a single mitotic division and contained many ?-H2AX foci, consistent with fragmented DNA. A prominent feature of such embryos was the establishment of two independent spindles following pronuclear fusion and thus a failure of the chromosomes to mix (syngamy). These generated binucleate 2-cell embryos. In the 10% of embryos that progressed to the 4-cell stage, division was so slow that compaction occurred prematurely. No embryo development to the blastocyst stage was ever observed. We conclude that Fzr1 is a surprisingly essential gene involved in the establishment of a single spindle from the two pronuclei in 1-cell embryos as well as being involved in the maintenance of genomic integrity during the mitotic divisions of early mammalian embryos.

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More information

e-pub ahead of print date: 24 October 2012
Published date: 15 December 2012
Keywords: mammalian embryos, meiosis, oocytes, mitosis, syngamy compaction
Organisations: Centre for Biological Sciences

Identifiers

Local EPrints ID: 349640
URI: http://eprints.soton.ac.uk/id/eprint/349640
ISSN: 0021-9533
PURE UUID: 65b5accd-bbcf-446f-9a56-2abd088c698a
ORCID for KT Jones: ORCID iD orcid.org/0000-0002-0294-0851

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Date deposited: 07 Mar 2013 16:30
Last modified: 14 Mar 2024 13:16

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Contributors

Author: MKY Seah
Author: JE Holt
Author: I García-Higuera
Author: S Moreno
Author: KT Jones ORCID iD

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