Literature DB >> 19887567

Deletion of the novel oocyte-enriched gene, Gpr149, leads to increased fertility in mice.

Mark A Edson1, Yi-Nan Lin, Martin M Matzuk.   

Abstract

Through in silico subtraction and microarray analysis, we identified mouse Gpr149, a novel, oocyte-enriched transcript that encodes a predicted orphan G-protein-coupled receptor (GPR). Phylogenetic analysis of GPR149 from fish to mammals suggests that it is widely conserved in vertebrates. By multitissue RT-PCR analysis, we found that Gpr149 is highly expressed in the ovary and also in the brain and the digestive tract at low levels. Gpr149 levels are low in newborn ovaries but increase throughout folliculogenesis. In the ovary, we found that granulosa cells did not express Gpr149, whereas germinal vesicle and meiosis II stage oocytes showed high levels of Gpr149 expression. After fertilization, Gpr149 expression declined, becoming undetectable by the two-cell stage. To study the function of GPR149 in oocyte growth and maturation, we generated Gpr149 null mice. Surprisingly, Gpr149 null mice are viable and have normal folliculogenesis, but demonstrate increased fertility, enhanced ovulation, increased oocyte Gdf9 mRNA levels, and increased levels of FSH receptor and cyclin D2 mRNA levels in granulosa cells. Thus, Gpr149 null mice are one of the few models with enhanced fertility, and GPR149 could be a target for small molecules to enhance fertility in the assisted reproductive technology clinic.

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Year:  2009        PMID: 19887567      PMCID: PMC2803152          DOI: 10.1210/en.2009-0760

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  48 in total

Review 1.  Oocyte-expressed genes affecting ovulation rate.

Authors:  K P McNatty; P Smith; L G Moore; K Reader; S Lun; J P Hanrahan; N P Groome; M Laitinen; O Ritvos; J L Juengel
Journal:  Mol Cell Endocrinol       Date:  2005-04-29       Impact factor: 4.102

2.  Efficient in vivo manipulation of mouse genomic sequences at the zygote stage.

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3.  The Gs-linked receptor GPR3 maintains meiotic arrest in mammalian oocytes.

Authors:  Lisa M Mehlmann; Yoshinaga Saeki; Shigeru Tanaka; Thomas J Brennan; Alexei V Evsikov; Frank L Pendola; Barbara B Knowles; John J Eppig; Laurinda A Jaffe
Journal:  Science       Date:  2004-12-10       Impact factor: 47.728

4.  Premature ovarian aging in mice deficient for Gpr3.

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Journal:  Proc Natl Acad Sci U S A       Date:  2005-06-13       Impact factor: 11.205

5.  Transcript profiling during mouse oocyte development and the effect of gonadotropin priming and development in vitro.

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Journal:  Dev Biol       Date:  2005-10-05       Impact factor: 3.582

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Authors:  R Buccione; B C Vanderhyden; P J Caron; J J Eppig
Journal:  Dev Biol       Date:  1990-03       Impact factor: 3.582

7.  The G-protein-coupled receptors GPR3 and GPR12 are involved in cAMP signaling and maintenance of meiotic arrest in rodent oocytes.

Authors:  Mary Hinckley; Sergio Vaccari; Kathleen Horner; Ruby Chen; Marco Conti
Journal:  Dev Biol       Date:  2005-10-17       Impact factor: 3.582

8.  Cyclin D2 is an FSH-responsive gene involved in gonadal cell proliferation and oncogenesis.

Authors:  P Sicinski; J L Donaher; Y Geng; S B Parker; H Gardner; M Y Park; R L Robker; J S Richards; L K McGinnis; J D Biggers; J J Eppig; R T Bronson; S J Elledge; R A Weinberg
Journal:  Nature       Date:  1996-12-05       Impact factor: 49.962

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Journal:  Biochem J       Date:  1995-08-01       Impact factor: 3.857

10.  Regulation of meiotic prophase arrest in mouse oocytes by GPR3, a constitutive activator of the Gs G protein.

Authors:  Leon Freudzon; Rachael P Norris; Arthur R Hand; Shigeru Tanaka; Yoshinaga Saeki; Teresa L Z Jones; Mark M Rasenick; Catherine H Berlot; Lisa M Mehlmann; Laurinda A Jaffe
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  11 in total

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Journal:  Br J Pharmacol       Date:  2013-12       Impact factor: 8.739

2.  Granulosa cell-expressed BMPR1A and BMPR1B have unique functions in regulating fertility but act redundantly to suppress ovarian tumor development.

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Journal:  Mol Endocrinol       Date:  2010-04-02

3.  The testis-enriched histone demethylase, KDM4D, regulates methylation of histone H3 lysine 9 during spermatogenesis in the mouse but is dispensable for fertility.

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Journal:  J Virol       Date:  2014-05-14       Impact factor: 5.103

5.  Two mouse lines selected for large litter size display different lifetime fecundities.

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8.  Contemporary genetic technologies and female reproduction.

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9.  Transcriptome analysis of chicken ES, blastodermal and germ cells reveals that chick ES cells are equivalent to mouse ES cells rather than EpiSC.

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Journal:  Stem Cell Res       Date:  2014-12-05       Impact factor: 2.020

10.  Genome-Wide Analyses Suggest Mechanisms Involving Early B-Cell Development in Canine IgA Deficiency.

Authors:  Mia Olsson; Katarina Tengvall; Marcel Frankowiack; Marcin Kierczak; Kerstin Bergvall; Erik Axelsson; Linda Tintle; Eliane Marti; Petra Roosje; Tosso Leeb; Åke Hedhammar; Lennart Hammarström; Kerstin Lindblad-Toh
Journal:  PLoS One       Date:  2015-07-30       Impact factor: 3.240

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