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

First Author  Ball CB Year  2014
Journal  PLoS One Volume  9
Issue  5 Pages  e97324
PubMed ID  24830504 Mgi Jnum  J:217353
Mgi Id  MGI:5613784 Doi  10.1371/journal.pone.0097324
Citation  Ball CB, et al. (2014) The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation. PLoS One 9(5):e97324
abstractText  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, DeltaN-ZFP36L2, leads to fertilized eggs that arrest at the two-cell stage. Interestingly, homozygous DeltaN-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 DeltaN-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 DeltaN-Zfp36l2 oocytes in the 129S6/SvEvTac strain matured ex vivo, suggesting a defect on the oocyte meiotic maturation process. Treatment of DeltaN-Zfp36l2 oocytes with a PKA inhibitor partially rescued the meiotic arrested oocytes. Furthermore, cAMP levels were increased in DeltaN-Zfp36l2 oocytes, linking the cAMP/PKA pathway and DeltaN-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 DeltaN-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.
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