Literature DB >> 23401597

Expression of fragile X mental retardation protein and Fmr1 mRNA during folliculogenesis in the rat.

Ianina Ferder1, Fernanda Parborell, Victoria Sundblad, Violeta Chiauzzi, Karina Gómez, Eduardo H Charreau, Marta Tesone, Liliana Dain.   

Abstract

Fragile X mental retardation protein (FMRP) belongs to a small family of RNA-binding proteins. Its absence or inactivity is responsible for fragile X syndrome, the most common cause of inherited mental retardation. Despite its ubiquitous expression, FMRP function and expression remain almost understudied in non-neuronal tissues, though previous studies on germline development during oogenesis may suggest a special function of this protein also in ovarian tissue. In addition, the well-documented association of FMR1 premutation state with fragile X-related premature ovarian insufficiency adds interest to the role of FMRP in ovarian physiology. The aim of the present work was to investigate the expression of Fmr1 mRNA and its protein, FMRP, at different stages of rat follicular development. By immunohistochemical studies we demonstrated FMRP expression in granulosa, theca and germ cells in all stages of follicular development. In addition, changes in Fmr1 expression, both at the protein and mRNA levels, were observed. FMRP levels increased upon follicular development while preantral and early antral follicles presented similar levels of Fmr1 transcripts with decreased expression in preovulatory follicles. These observations suggest that Fmr1 expression in the ovary is regulated at different and perhaps independent levels. In addition, our results show expression of at least four different isoforms of FMRP during all stages of follicular growth with expression patterns that differ from those observed in brain and testis. Our study shows a regulated expression of Fmr1, both at mRNA and protein levels, during rat follicular development.

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Year:  2013        PMID: 23401597     DOI: 10.1530/REP-12-0305

Source DB:  PubMed          Journal:  Reproduction        ISSN: 1470-1626            Impact factor:   3.906


  9 in total

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3.  Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency.

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Journal:  Hum Reprod       Date:  2015-11-03       Impact factor: 6.918

Review 4.  Ovarian Follicular Theca Cell Recruitment, Differentiation, and Impact on Fertility: 2017 Update.

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Review 5.  Use of model systems to understand the etiology of fragile X-associated primary ovarian insufficiency (FXPOI).

Authors:  Stephanie L Sherman; Eliza C Curnow; Charles A Easley; Peng Jin; Renate K Hukema; Maria Isabel Tejada; Rob Willemsen; Karen Usdin
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6.  Reduced RNA expression of the FMR1 gene in women with low (CGGn<26) repeats.

Authors:  Qi Wang; David H Barad; Sarah K Darmon; Vitaly A Kushnir; Yan-Guang Wu; Emanuela Lazzaroni-Tealdi; Lin Zhang; David F Albertini; Norbert Gleicher
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7.  Utilizing FMR1 gene mutations as predictors of treatment success in human in vitro fertilization.

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Journal:  PLoS One       Date:  2014-07-14       Impact factor: 3.240

8.  How the FMR1 gene became relevant to female fertility and reproductive medicine.

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9.  Developmental Dioxin Exposure Alters the Methylome of Adult Male Zebrafish Gonads.

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  9 in total

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