journal article·2013-02

The Distribution and Possible Role of ERK8 in Mouse Oocyte Meiotic Maturation and Early Embryo Cleavage

Shang-Wu Yang, Hao Huang, Chen Gao, Lei Chen, Shu-Tao Qi, Fei Lin, Jian-Xin Wang, Yi Hou, Fu-Qi Xing, Qing-Yuan Sun

Microscopy and Microanalysis· Volume 19· Issue 1
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Abstract

Abstract It is well known that extracellular signal-regulated kinase 8 (ERK8) plays pivotal roles in various mitotic events. But its physiological roles in oocyte meiotic maturation remain unclear. In this study, we found that although no specific ERK8 signal was detected in oocyte at the germinal vesicle stage, ERK8 began to migrate to the periphery of chromosomes shortly after germinal vesicle breakdown. At prometaphase I, metaphase I (MI), anaphase I, telophase I, and metaphase II (MII) stages, ERK8 was stably detected at the spindles. By taxol treatment, we clarified that the ERK8 signal was stained on the spindle fibers as well as microtubule asters in MI and MII oocytes. In fertilized eggs, the ERK8 signal was not observed in the two pronuclei stages. At prometaphase, metaphase, and anaphase of the first mitosis, ERK8 was detected on the mitotic spindle. ERK8 knock down by antibody microinjection and specific siRNA caused abnormal spindles, failed chromosome congression, and decreased first polar body extrusion. Taken together, our results suggest that ERK8 plays an important role in spindle organization during mouse oocyte meiotic maturation and early embryo cleavage.
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Research context

OpenAlex topics: Reproductive Biology and Fertility · Microtubule and mitosis dynamics · Kruppel-like factors research

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References (39)

Show source-provided references
1. 10.1074/jbc.M11248320010.1074/jbc.M112483200 ↗
2. 10.1262/jrd.2003410.1262/jrd.20034 ↗
3. 10.1006/dbio.1993.119210.1006/dbio.1993.1192 ↗
4. 10.1371/journal.pone.001124710.1371/journal.pone.0011247 ↗
5. 10.1016/j.cell.2006.11.05310.1016/j.cell.2006.11.053 ↗
6. 10.1158/0008-5472.CAN-09-430610.1158/0008-5472.CAN-09-4306 ↗
7. 10.4161/cc.8.20.988510.4161/cc.8.20.9885 ↗
8. 10.1016/S0074-7696(04)38001-010.1016/S0074-7696(04)38001-0 ↗
9. 10.1017/S143192761009445610.1017/S1431927610094456 ↗
10. 10.1083/jcb.20051002810.1083/jcb.200510028 ↗
11. Mitogen-activated protein (MAP) kinase pathways: Regulation and physiological functions
12. 10.1146/annurev.biochem.69.1.9510.1146/annurev.biochem.69.1.95 ↗
13. 10.1016/0955-0674(95)80063-810.1016/0955-0674(95)80063-8 ↗
14. 10.1007/s00418-008-0427-610.1007/s00418-008-0427-6 ↗
15. 10.1074/jbc.M51339720010.1074/jbc.M513397200 ↗
16. 10.1016/j.cellsig.2004.05.00410.1016/j.cellsig.2004.05.004 ↗
17. 10.1016/j.cell.2007.06.02510.1016/j.cell.2007.06.025 ↗
18. 10.1007/s10815-010-9456-x10.1007/s10815-010-9456-x ↗
19. 10.1186/1747-1028-6-1710.1186/1747-1028-6-17 ↗
20. 10.4161/cc.2027910.4161/cc.20279 ↗
21. 10.1111/j.1747-0285.2011.01156.x10.1111/j.1747-0285.2011.01156.x ↗
22. 10.1017/S143192761100027410.1017/S1431927611000274 ↗
23. 10.1016/j.cell.2006.05.02510.1016/j.cell.2006.05.025 ↗
24. 10.1017/S143192760808034310.1017/S1431927608080343 ↗
25. 10.1083/jcb.20100212410.1083/jcb.201002124 ↗
26. 10.1016/S0065-230X(08)60765-410.1016/S0065-230X(08)60765-4 ↗
27. 10.1095/biolreprod.108.06924510.1095/biolreprod.108.069245 ↗
28. 10.1016/j.ydbio.2010.01.00910.1016/j.ydbio.2010.01.009 ↗
29. 10.1016/S0955-0674(97)80061-010.1016/S0955-0674(97)80061-0 ↗
30. 10.1017/S143192761100001810.1017/S1431927611000018 ↗
31. 10.1095/biolreprod67.2.54610.1095/biolreprod67.2.546 ↗
32. 10.1007/s00709-010-0205-x10.1007/s00709-010-0205-x ↗
33. 10.1002/mrd.2138010.1002/mrd.21380 ↗
34. 10.1095/biolreprod.108.06964110.1095/biolreprod.108.069641 ↗
35. 10.1095/biolreprod.103.02515510.1095/biolreprod.103.025155 ↗
36. 10.1016/S0074-7696(07)65003-710.1016/S0074-7696(07)65003-7 ↗
37. 10.1002/mrd.2061310.1002/mrd.20613 ↗
38. 10.1002/dvdy.2272510.1002/dvdy.22725 ↗
39. 10.1016/S0955-0674(03)00046-210.1016/S0955-0674(03)00046-2 ↗