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ePAD, an oocyte and early embryo-abundant peptidylarginine deiminase-like protein that localizes to egg cytoplasmic sheets.

Publication ,  Journal Article
Wright, PW; Bolling, LC; Calvert, ME; Sarmento, OF; Berkeley, EV; Shea, MC; Hao, Z; Jayes, FC; Bush, LA; Shetty, J; Shore, AN; Reddi, PP ...
Published in: Dev Biol
April 1, 2003

Selected for its high relative abundance, a protein spot of MW approximately 75 kDa, pI 5.5 was cored from a Coomassie-stained two-dimensional gel of proteins from 2850 zona-free metaphase II mouse eggs and analyzed by tandem mass spectrometry (TMS), and novel microsequences were identified that indicated a previously uncharacterized egg protein. A 2.4-kb cDNA was then amplified from a mouse ovarian adapter-ligated cDNA library by RACE-PCR, and a unique 2043-bp open reading frame was defined encoding a 681-amino-acid protein. Comparison of the deduced amino acid sequence with the nonredundant database demonstrated that the protein was approximately 40% identical to the calcium-dependent peptidylarginine deiminase (PAD) enzyme family. Northern blotting, RT-PCR, and in situ hybridization analyses indicated that the protein was abundantly expressed in the ovary, weakly expressed in the testis, and absent from other tissues. Based on the homology with PADs and its oocyte-abundant expression pattern, the protein was designated ePAD, for egg and embryo-abundant peptidylarginine deiminase-like protein. Anti-recombinant ePAD monospecific antibodies localized the molecule to the cytoplasm of oocytes in primordial, primary, secondary, and Graafian follicles in ovarian sections, while no other ovarian cell type was stained. ePAD was also expressed in the immature oocyte, mature egg, and through the blastocyst stage of embryonic development, where expression levels began to decrease. Immunoelectron microscopy localized ePAD to egg cytoplasmic sheets, a unique keratin-containing intermediate filament structure found only in mammalian eggs and in early embryos, and known to undergo reorganization at critical stages of development. Previous reports that PAD-mediated deimination of epithelial cell keratin results in cytoskeletal remodeling suggest a possible role for ePAD in cytoskeletal reorganization in the egg and early embryo.

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Published In

Dev Biol

DOI

ISSN

0012-1606

Publication Date

April 1, 2003

Volume

256

Issue

1

Start / End Page

73 / 88

Location

United States

Related Subject Headings

  • Solubility
  • Sequence Homology, Amino Acid
  • Recombinant Proteins
  • Protein-Arginine Deiminases
  • Protein-Arginine Deiminase Type 4
  • Pregnancy
  • Ovary
  • Oocytes
  • Molecular Sequence Data
  • Microscopy, Immunoelectron
 

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Wright, P. W., Bolling, L. C., Calvert, M. E., Sarmento, O. F., Berkeley, E. V., Shea, M. C., … Coonrod, S. A. (2003). ePAD, an oocyte and early embryo-abundant peptidylarginine deiminase-like protein that localizes to egg cytoplasmic sheets. Dev Biol, 256(1), 73–88. https://doi.org/10.1016/s0012-1606(02)00126-4
Wright, Paul W., Laura C. Bolling, Meredith E. Calvert, Olga F. Sarmento, Elizabeth V. Berkeley, Margaret C. Shea, Zhonglin Hao, et al. “ePAD, an oocyte and early embryo-abundant peptidylarginine deiminase-like protein that localizes to egg cytoplasmic sheets.Dev Biol 256, no. 1 (April 1, 2003): 73–88. https://doi.org/10.1016/s0012-1606(02)00126-4.
Wright PW, Bolling LC, Calvert ME, Sarmento OF, Berkeley EV, Shea MC, et al. ePAD, an oocyte and early embryo-abundant peptidylarginine deiminase-like protein that localizes to egg cytoplasmic sheets. Dev Biol. 2003 Apr 1;256(1):73–88.
Wright, Paul W., et al. “ePAD, an oocyte and early embryo-abundant peptidylarginine deiminase-like protein that localizes to egg cytoplasmic sheets.Dev Biol, vol. 256, no. 1, Apr. 2003, pp. 73–88. Pubmed, doi:10.1016/s0012-1606(02)00126-4.
Wright PW, Bolling LC, Calvert ME, Sarmento OF, Berkeley EV, Shea MC, Hao Z, Jayes FC, Bush LA, Shetty J, Shore AN, Reddi PP, Tung KS, Samy E, Allietta MM, Sherman NE, Herr JC, Coonrod SA. ePAD, an oocyte and early embryo-abundant peptidylarginine deiminase-like protein that localizes to egg cytoplasmic sheets. Dev Biol. 2003 Apr 1;256(1):73–88.
Journal cover image

Published In

Dev Biol

DOI

ISSN

0012-1606

Publication Date

April 1, 2003

Volume

256

Issue

1

Start / End Page

73 / 88

Location

United States

Related Subject Headings

  • Solubility
  • Sequence Homology, Amino Acid
  • Recombinant Proteins
  • Protein-Arginine Deiminases
  • Protein-Arginine Deiminase Type 4
  • Pregnancy
  • Ovary
  • Oocytes
  • Molecular Sequence Data
  • Microscopy, Immunoelectron