Expression of RNA-binding proteins DND1 and FXR1 in the porcine ovary, and during oocyte maturation and early embryo development

被引:22
作者
Yang, Cai-Xia [1 ,2 ]
Wright, Elane C. [1 ]
Ross, Jason W. [1 ,2 ]
机构
[1] Iowa State Univ, Dept Anim Sci, Ames, IA 50011 USA
[2] Iowa State Univ, Ctr Integrated Anim Genom, Ames, IA 50011 USA
基金
美国食品与农业研究所;
关键词
GENE-EXPRESSION; GERM-CELL; DEAD-END; ANIMAL DEVELOPMENT; MESSENGER-RNA; STEM-CELLS; CUMULUS CELLS; MICRORNAS; DIFFERENTIATION; IDENTIFICATION;
D O I
10.1002/mrd.22059
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The porcine oocyte and early embryo are transcriptionally quiescent following germinal vesicle breakdown in the oocyte and prior to activation of the embryonic genome, at approximately the 4-cell stage of development. Despite a lack of new transcription, mRNA and protein repertoires are subject to regulation during this time. One potential mechanism of regulation is through the functional activity of miRNAs and/or the presence of specific RNA-binding proteins. Both DND1 (dead end homolog 1) and FXR1 (fragile-X-mental retardation-related protein 1) are RNA-binding proteins that have been demonstrated to impact miRNA-mediated, post-transcriptional gene regulation. The objective was to characterize the presence and the expression changes in DND1 and FXR1 during pig oocyte maturation and early embryo development. DND1 and FXR1 expression were evaluated in oocytes and cumulus cells during meiotic progression and in 4-cell stage embryos using quantitative RT-PCR, Western blot analysis, and immunostaining. These data demonstrate DND1 and FXR1 mRNA are expressed in the maturing oocyte and early in vitro-fertilized embryos, with significantly less DND1 in 4-cell stage embryos as compared to germinal vesicle and metaphase II-arrested oocytes. Based on immunohistochemistry, DND1 protein abundance is greater in secondary follicles in comparison to primary and tertiary follicles. Using ribonucleoprotein immunoprecipitation from germinal vesicle-stage oocytes, DND1 was demonstrated to interact with several mRNAs associated with pluripotency. This work provides a better understanding of the biological relevance of DND1 and FXR1 during female gametogenesis and embryo development in pigs.Mol. Reprod. Dev. 79: 541-552, 2012. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:541 / 552
页数:12
相关论文
共 53 条
[1]  
Abramoff M.D., 2004, Biophotonics International, V11, P36
[2]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[3]   The mouse dead-end gene isoform α is necessary for germ cell and embryonic viability [J].
Bhattacharya, Chitralekha ;
Aggarwal, Sita ;
Zhu, Rui ;
Kumar, Madhu ;
Zhao, Ming ;
Meistrich, Marvin L. ;
Matin, Angabin .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 355 (01) :194-199
[4]   MicroRNA expression profiling of elongated cloned and in vitro-fertilized bovine embryos [J].
Castro, F. O. ;
Sharbati, S. ;
Rodriguez-Alvarez, L. L. ;
Cox, J. F. ;
Hultschig, C. ;
Einspanier, R. .
THERIOGENOLOGY, 2010, 73 (01) :71-85
[5]   Fragile X protein family member FXR1P is regulated by microRNAs [J].
Cheever, Anne ;
Blackwell, Ernest ;
Ceman, Stephanie .
RNA, 2010, 16 (08) :1530-1539
[6]   Gene expression and chromatin organization during mouse oocyte growth [J].
Christians, E ;
Boiani, M ;
Garagna, S ;
Dessy, C ;
Redi, CA ;
Renard, JP ;
Zuccotti, M .
DEVELOPMENTAL BIOLOGY, 1999, 207 (01) :76-85
[7]   Regulation of male germ cell cycle arrest and differentiation by DND1 is modulated by genetic background [J].
Cook, Matthew S. ;
Munger, Steven C. ;
Nadeau, Joseph H. ;
Capel, Blanche .
DEVELOPMENT, 2011, 138 (01) :23-32
[8]   Fragile X protein controls the efficacy of mRNA transport in Drosophila neurons [J].
Estes, Patricia S. ;
O'Shea, Michele ;
Clasen, Sara ;
Zarnescu, Daniela C. .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2008, 39 (02) :170-179
[9]   Protein kinase C and mitogen-activated protein kinase cascade in mouse cumulus cells: Cross talk and effect on meiotic resumption of oocyte [J].
Fan, HY ;
Huo, LJ ;
Chen, DY ;
Schatten, H ;
Sun, QY .
BIOLOGY OF REPRODUCTION, 2004, 70 (04) :1178-1187
[10]   Zebrafish MiR-430 promotes deadenylation and clearance of maternal mRNAs [J].
Giraldez, AJ ;
Mishima, Y ;
Rihel, J ;
Grocock, RJ ;
Van Dongen, S ;
Inoue, K ;
Enright, AJ ;
Schier, AF .
SCIENCE, 2006, 312 (5770) :75-79