Abstract

ObjectiveThe early growth response (Egr) family consists of four members (Egr1, Egr2, Egr3, and Egr4) that are zinc finger transcription factors. Among them, Egr3 is involved in transcriptional regulation of target genes during muscle spindle formation and neurite outgrowth. We previously showed that the immunoreactive Egr3 is localized on oocyte spindle and accumulate near the microtubule organizing center during meiosis I in mice. Egr3 was also shown to be localized on spermatocytes. We herein investigated if Egr3 is expressed in mouse gonads and if Egr3 blockade results in any defect in oocyte maturation.MethodsExpression of Egr3 in mouse gonads was examined by reverse transcription-polymerase chain reaction. Full-length Egr3 and truncated Egr3 (ΔEgr3) complementary RNAs (cRNAs) with Xpress tag at N-terminus and DsRed2 at C-terminus, and small interfering RNA (siRNA) targeting Egr3 were microinjected into mouse oocytes at germinal vesicle stage. Localization of microinjected Egr3 was examined by confocal live imaging and immunofluorescence staining.ResultsEgr3 mRNA was detected in mouse ovaries and testes from 1 to 4 week-old mice. An uncharacterized longer transcript containing 5′untranslated region was also detected in 3 and 4 week-old gonads. Microinjected Xpress-Egr3-DsRed2 or Xpress-ΔEgr3-DsRed2 localized to nuclei and chromosomes during meiotic progression. Microinjection of these cRNAs or Egr3 siRNA in oocytes did not affect meiotic maturation. Immunofluorescence staining of Egr3 in Xpress-ΔEgr3-DsRed2-injected oocytes showed a positive signal only on meiotic spindle, suggesting that this antibody does not detect endogenous or exogenous Egr3 in mouse oocytes.ConclusionThe results show that Egr3 localizes to chromosomes during meiotic progression and that certain antibodies may not faithfully represent localization of target proteins in oocytes. Egr3 seems to be dispensable during oocyte maturation in mice.

Highlights

  • The early growth response (Egr) family of zinc finger transcription factors regulates critical genetic programs in cellular growth, differentiation, and function [1,2]

  • Egr1 regulates expression of the luteinizing hormone beta subunit, and Egr1 deficient mice suffer from female infertility resulting from hormone insufficiency [3]

  • Reverse transcription-polymerase chain reaction (RT-PCR) analysis showed that Egr3 mRNA is ex­ pressed in ovaries and testes in all groups

Read more

Summary

Objective

The early growth response (Egr) family consists of four members (Egr, Egr, Egr, and Egr4) that are zinc finger transcription factors. We investigated if Egr is expressed in mouse gonads and if Egr blockade results in any defect in oocyte maturation. Results: Egr mRNA was detected in mouse ovaries and testes from 1 to 4 week-old mice. Microinjected Xpress-Egr3-DsRed or Xpress-ΔEgr3-DsRed localized to nuclei and chromosomes during meiotic progression. Microinjection of these cRNAs or Egr siRNA in oocytes did not affect meiotic maturation. Immunofluorescence staining of Egr in Xpress-ΔEgr3-DsRed2-injected oocytes showed a positive signal only on meiotic spindle, sugges­ ting that this antibody does not detect endogenous or exogenous Egr in mouse oocytes. Conclusion: The results show that Egr localizes to chromosomes during meiotic progression and that certain antibodies may not faithfully represent localization of target proteins in oocytes. Egr seems to be dispensable during oocyte maturation in mice

INTRODUCTION
MATERIALS AND METHODS
F: TCA ATG GAG TAA GCC CAA AG
RESULTS
DISCUSSION
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call