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Francis Bergeron Reproduction, Department of Obstetrics and Gynecology, Perinatal and Child Health, CHUQ Research Centre, CHUL Room T1-49, 2705 Laurier Boulevard, Québec, Québec, Canada G1V 4G2

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Edward T Bagu Reproduction, Department of Obstetrics and Gynecology, Perinatal and Child Health, CHUQ Research Centre, CHUL Room T1-49, 2705 Laurier Boulevard, Québec, Québec, Canada G1V 4G2

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Jacques J Tremblay Reproduction, Department of Obstetrics and Gynecology, Perinatal and Child Health, CHUQ Research Centre, CHUL Room T1-49, 2705 Laurier Boulevard, Québec, Québec, Canada G1V 4G2
Reproduction, Department of Obstetrics and Gynecology, Perinatal and Child Health, CHUQ Research Centre, CHUL Room T1-49, 2705 Laurier Boulevard, Québec, Québec, Canada G1V 4G2

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information regarding the molecular mechanisms that regulate its expression in Leydig cells. However, in vascular smooth muscle cells (VSMC), expression of the rat Pdgfra gene is under the positive regulatory influence of the transcription factor specificity

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JME-10-0145
Volume/Issue:
Volume 46: Issue 2
Free access
V X Jin Human Cancer Genetics Program, Comprehensive Cancer Center, Department of Molecular Virology, Immunology and Medical Genetics, Ohio State University, 420 W 12th Avenue, TMRF 524A, Columbus, Ohio 43210, USA

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H Sun Human Cancer Genetics Program, Comprehensive Cancer Center, Department of Molecular Virology, Immunology and Medical Genetics, Ohio State University, 420 W 12th Avenue, TMRF 524A, Columbus, Ohio 43210, USA

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T T Pohar Human Cancer Genetics Program, Comprehensive Cancer Center, Department of Molecular Virology, Immunology and Medical Genetics, Ohio State University, 420 W 12th Avenue, TMRF 524A, Columbus, Ohio 43210, USA

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S Liyanarachchi Human Cancer Genetics Program, Comprehensive Cancer Center, Department of Molecular Virology, Immunology and Medical Genetics, Ohio State University, 420 W 12th Avenue, TMRF 524A, Columbus, Ohio 43210, USA

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S K Palaniswamy Human Cancer Genetics Program, Comprehensive Cancer Center, Department of Molecular Virology, Immunology and Medical Genetics, Ohio State University, 420 W 12th Avenue, TMRF 524A, Columbus, Ohio 43210, USA

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T H-M Huang Human Cancer Genetics Program, Comprehensive Cancer Center, Department of Molecular Virology, Immunology and Medical Genetics, Ohio State University, 420 W 12th Avenue, TMRF 524A, Columbus, Ohio 43210, USA

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R V Davuluri Human Cancer Genetics Program, Comprehensive Cancer Center, Department of Molecular Virology, Immunology and Medical Genetics, Ohio State University, 420 W 12th Avenue, TMRF 524A, Columbus, Ohio 43210, USA

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has been associated with endocrine diseases such as breast and prostate cancers, and the action of ERs is linked to the growth promotion and invasion of breast cancer cells ( Pearce & Jordan 2004 ). ERs modulate the transcription of target genes when

Article Type:
Research Article
DOI:
https://doi.org/10.1677/jme.1.01839
Volume/Issue:
Volume 35: Issue 2
Free access
Maëlle Pannetier Biologie du Développement et de la Reproduction – UMR 1198 INRA-ENVA, Bât. J Poly, 78350 Jouy-en-Josas, France
Physiologie de la Reproduction et des Comportements – UMR 6175 INRA-CNRS-Université de Tours, Haras Nationaux, 37380 Nouzilly, France
INSERM U709 Génomique et Epigénétique des Pathologies Placentaires (Ex. U361), Hôpital Cochin, Pavillon Baudelocque, 123 Bd de Port Royal, 75014 Paris, France

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Stéphane Fabre Biologie du Développement et de la Reproduction – UMR 1198 INRA-ENVA, Bât. J Poly, 78350 Jouy-en-Josas, France
Physiologie de la Reproduction et des Comportements – UMR 6175 INRA-CNRS-Université de Tours, Haras Nationaux, 37380 Nouzilly, France
INSERM U709 Génomique et Epigénétique des Pathologies Placentaires (Ex. U361), Hôpital Cochin, Pavillon Baudelocque, 123 Bd de Port Royal, 75014 Paris, France

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Frank Batista Biologie du Développement et de la Reproduction – UMR 1198 INRA-ENVA, Bât. J Poly, 78350 Jouy-en-Josas, France
Physiologie de la Reproduction et des Comportements – UMR 6175 INRA-CNRS-Université de Tours, Haras Nationaux, 37380 Nouzilly, France
INSERM U709 Génomique et Epigénétique des Pathologies Placentaires (Ex. U361), Hôpital Cochin, Pavillon Baudelocque, 123 Bd de Port Royal, 75014 Paris, France

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Ayhan Kocer Biologie du Développement et de la Reproduction – UMR 1198 INRA-ENVA, Bât. J Poly, 78350 Jouy-en-Josas, France
Physiologie de la Reproduction et des Comportements – UMR 6175 INRA-CNRS-Université de Tours, Haras Nationaux, 37380 Nouzilly, France
INSERM U709 Génomique et Epigénétique des Pathologies Placentaires (Ex. U361), Hôpital Cochin, Pavillon Baudelocque, 123 Bd de Port Royal, 75014 Paris, France

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Lauriane Renault Biologie du Développement et de la Reproduction – UMR 1198 INRA-ENVA, Bât. J Poly, 78350 Jouy-en-Josas, France
Physiologie de la Reproduction et des Comportements – UMR 6175 INRA-CNRS-Université de Tours, Haras Nationaux, 37380 Nouzilly, France
INSERM U709 Génomique et Epigénétique des Pathologies Placentaires (Ex. U361), Hôpital Cochin, Pavillon Baudelocque, 123 Bd de Port Royal, 75014 Paris, France

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Geneviève Jolivet Biologie du Développement et de la Reproduction – UMR 1198 INRA-ENVA, Bât. J Poly, 78350 Jouy-en-Josas, France
Physiologie de la Reproduction et des Comportements – UMR 6175 INRA-CNRS-Université de Tours, Haras Nationaux, 37380 Nouzilly, France
INSERM U709 Génomique et Epigénétique des Pathologies Placentaires (Ex. U361), Hôpital Cochin, Pavillon Baudelocque, 123 Bd de Port Royal, 75014 Paris, France

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Béatrice Mandon-Pépin Biologie du Développement et de la Reproduction – UMR 1198 INRA-ENVA, Bât. J Poly, 78350 Jouy-en-Josas, France
Physiologie de la Reproduction et des Comportements – UMR 6175 INRA-CNRS-Université de Tours, Haras Nationaux, 37380 Nouzilly, France
INSERM U709 Génomique et Epigénétique des Pathologies Placentaires (Ex. U361), Hôpital Cochin, Pavillon Baudelocque, 123 Bd de Port Royal, 75014 Paris, France

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Corinne Cotinot Biologie du Développement et de la Reproduction – UMR 1198 INRA-ENVA, Bât. J Poly, 78350 Jouy-en-Josas, France
Physiologie de la Reproduction et des Comportements – UMR 6175 INRA-CNRS-Université de Tours, Haras Nationaux, 37380 Nouzilly, France
INSERM U709 Génomique et Epigénétique des Pathologies Placentaires (Ex. U361), Hôpital Cochin, Pavillon Baudelocque, 123 Bd de Port Royal, 75014 Paris, France

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Reiner Veitia Biologie du Développement et de la Reproduction – UMR 1198 INRA-ENVA, Bât. J Poly, 78350 Jouy-en-Josas, France
Physiologie de la Reproduction et des Comportements – UMR 6175 INRA-CNRS-Université de Tours, Haras Nationaux, 37380 Nouzilly, France
INSERM U709 Génomique et Epigénétique des Pathologies Placentaires (Ex. U361), Hôpital Cochin, Pavillon Baudelocque, 123 Bd de Port Royal, 75014 Paris, France

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Eric Pailhoux Biologie du Développement et de la Reproduction – UMR 1198 INRA-ENVA, Bât. J Poly, 78350 Jouy-en-Josas, France
Physiologie de la Reproduction et des Comportements – UMR 6175 INRA-CNRS-Université de Tours, Haras Nationaux, 37380 Nouzilly, France
INSERM U709 Génomique et Epigénétique des Pathologies Placentaires (Ex. U361), Hôpital Cochin, Pavillon Baudelocque, 123 Bd de Port Royal, 75014 Paris, France

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Introduction Recent accumulating evidence indicates that the transcription factor FOXL2 is a crucial actor in early ovarian differentiation and maintenance. Natural mutations affecting FOXL2 have been shown to be involved in two

Article Type:
Research Article
DOI:
https://doi.org/10.1677/jme.1.01947
Volume/Issue:
Volume 36: Issue 3
Free access
Raghunath Chatterjee
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Paramita Bhattacharya
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Oksana Gavrilova Laboratory of Metabolism, Mouse Metabolism Laboratory, Physics Department, SAIC Frederick, Veterinary Resources Program, National Cancer Institute, National Institutes of Health, Building 37, Room 3128, Bethesda, Maryland 20892, USA

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Kimberly Glass Laboratory of Metabolism, Mouse Metabolism Laboratory, Physics Department, SAIC Frederick, Veterinary Resources Program, National Cancer Institute, National Institutes of Health, Building 37, Room 3128, Bethesda, Maryland 20892, USA

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Jaideep Moitra
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Max Myakishev
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Stephanie Pack Laboratory of Metabolism, Mouse Metabolism Laboratory, Physics Department, SAIC Frederick, Veterinary Resources Program, National Cancer Institute, National Institutes of Health, Building 37, Room 3128, Bethesda, Maryland 20892, USA

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William Jou Laboratory of Metabolism, Mouse Metabolism Laboratory, Physics Department, SAIC Frederick, Veterinary Resources Program, National Cancer Institute, National Institutes of Health, Building 37, Room 3128, Bethesda, Maryland 20892, USA

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Lionel Feigenbaum Laboratory of Metabolism, Mouse Metabolism Laboratory, Physics Department, SAIC Frederick, Veterinary Resources Program, National Cancer Institute, National Institutes of Health, Building 37, Room 3128, Bethesda, Maryland 20892, USA

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Michael Eckhaus Laboratory of Metabolism, Mouse Metabolism Laboratory, Physics Department, SAIC Frederick, Veterinary Resources Program, National Cancer Institute, National Institutes of Health, Building 37, Room 3128, Bethesda, Maryland 20892, USA

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Charles Vinson
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function of both the CCAAT-enhancer-binding protein (C/EBP) and the JUN families of transcription factors ( Vinson et al . 1993 ) implicated in adipocyte growth and development ( Herrera et al . 1989 , Linhart et al . 2001 ). The resulting TG mice, A

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JME-10-0172
Volume/Issue:
Volume 46: Issue 3
Free access
Z Tong
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G R Pitts
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D N Foster
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M E El Halawani
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ABSTRACT

The present study examined turkey prolactin (PRL) transcription and PRL mRNA stability during different reproductive stages. Nuclear run-on transcription assays were performed using isolated nuclei from pituitaries of turkeys at different reproductive stages. Meanwhile, cytoplasmic PRL mRNA and plasma PRL were measured by slot blot and RIA respectively. The PRL transcription, pituitary cytoplasmic PRL mRNA abundance and plasma PRL levels increased after photostimulation and peaked at the incubating stage (P<0·05). A decrease in PRL transcription, pituitary cytoplasmic PRL mRNA and plasma PRL (P<0·05) was observed during the transition from incubation to photorefractoriness. Nest-deprivation reduced circulating PRL (P<0·05), whereas pituitary cytoplasmic PRL mRNA and PRL transcription were not significantly altered from those in incubating birds (P>0·05). The half-life of PRL mRNA was determined in pituitaries of non-photostimulated, laying, incubating and photorefractory hens. Primary pituitary cell cultures were treated with the transcription inhibitor actinomycin-D and the decay of the pre-existing PRL mRNA was quantified using Northern blot analysis. The PRL mRNA half-life was 1·5- and 1·4-fold greater in incubating and laying birds respectively than in non-photostimulated turkeys (P<0·05). The half-life of PRL mRNA in photorefractory and incubating hens was similar in spite of great differences in pituitary PRL mRNA steady-state levels and PRL transcription. Our data suggest that photoinduced changes in pituitary PRL mRNA and plasma PRL are due to changes in both PRL transcription and PRL mRNA stability. Nest-deprivation inhibits the PRL releasing mechanism(s) independently of PRL transcription in turkeys.

Article Type:
Research Article
DOI:
https://doi.org/10.1677/jme.0.0180223
Volume/Issue:
Volume 18: Issue 3
Restricted access
Pulak R Manna Department of Cell Biology and Biochemistry Texas Tech University Health Sciences Center, Lubbock, Texas 79430, USA

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Douglas M Stocco Department of Cell Biology and Biochemistry Texas Tech University Health Sciences Center, Lubbock, Texas 79430, USA

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-mediated mechanisms that involve transcriptional induction. Despite our current knowledge surrounding the regulation of the StAR gene, a complete understanding of the cAMP-dependent signaling events involved in this process is still lacking. Transcriptional

Article Type:
Research Article
DOI:
https://doi.org/10.1677/JME-07-0065
Volume/Issue:
Volume 39: Issue 4
Free access
A Blondet Inserm U418-Inra UMR 1245 and IFR 62, Hôpital Debrousse and Claude Bernard University, Lyon, France

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J Gout Inserm U418-Inra UMR 1245 and IFR 62, Hôpital Debrousse and Claude Bernard University, Lyon, France

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P Durand Inserm U418-Inra UMR 1245 and IFR 62, Hôpital Debrousse and Claude Bernard University, Lyon, France

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M Bégeot Inserm U418-Inra UMR 1245 and IFR 62, Hôpital Debrousse and Claude Bernard University, Lyon, France

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D Naville Inserm U418-Inra UMR 1245 and IFR 62, Hôpital Debrousse and Claude Bernard University, Lyon, France

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transcriptional activation of the hMC4-R gene. Materials and methods Materials Penicillin, streptomycin, fetal calf serum (FCS), Dulbecco’s Modified Eagle’s Medium/Ham’s nutrient mixture (DMEM/F-12, 15 mM Hepes

Article Type:
Research Article
DOI:
https://doi.org/10.1677/jme.1.01614
Volume/Issue:
Volume 34: Issue 2
Free access
Syed Kashif Zaidi Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA
Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA

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Wen-Jun Shen Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA
Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA

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Stefanie Bittner Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA

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Alex Bittner Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA

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Mark P McLean Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA

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Jiahuai Han Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA

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Roger J Davis Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA

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Fredric B Kraemer Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA
Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA

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Salman Azhar Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA
Geriatric Research, Division of Endocrinology, Division of Gastroenterology and Hepatology, Department of Obstetrics and Gynecology, State Key Laboratory of Cellular Stress Biology, Program in Molecular Medicine, Education and Clinical Center (GRECC-182B), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, California 94304, USA

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. 2010 ). These isoforms differ in their organ/tissue distribution, regulation of kinase activation and subsequent phosphorylation of downstream substrates, kinases or transcription factors, and sensitivity to pharmacological inhibition by pyridinyl

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JME-13-0287
Volume/Issue:
Volume 53: Issue 1
Free access
M Udelhoven Department of Internal Medicine II, Center for Molecular Medicine Cologne (CMMC), and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Kerpener Strasse 62, 50937 Cologne, Germany

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U Leeser Department of Internal Medicine II, Center for Molecular Medicine Cologne (CMMC), and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Kerpener Strasse 62, 50937 Cologne, Germany

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S Freude Department of Internal Medicine II, Center for Molecular Medicine Cologne (CMMC), and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Kerpener Strasse 62, 50937 Cologne, Germany

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M M Hettich Department of Internal Medicine II, Center for Molecular Medicine Cologne (CMMC), and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Kerpener Strasse 62, 50937 Cologne, Germany

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M Laudes Department of Internal Medicine II, Center for Molecular Medicine Cologne (CMMC), and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Kerpener Strasse 62, 50937 Cologne, Germany

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J Schnitker Department of Internal Medicine II, Center for Molecular Medicine Cologne (CMMC), and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Kerpener Strasse 62, 50937 Cologne, Germany

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W Krone Department of Internal Medicine II, Center for Molecular Medicine Cologne (CMMC), and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Kerpener Strasse 62, 50937 Cologne, Germany

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M Schubert Department of Internal Medicine II, Center for Molecular Medicine Cologne (CMMC), and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Kerpener Strasse 62, 50937 Cologne, Germany

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abundance of every single IRS protein in a specific tissue. One of the most important aspects of protein expression is its transcriptional regulation in different tissues ( Vassen et al . 1999 ). The mechanisms leading to transcriptional activation of the

Article Type:
Research Article
DOI:
https://doi.org/10.1677/JME-08-0182
Volume/Issue:
Volume 44: Issue 2
Free access
Yi Lu Center for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People’s Republic of China
Shanghai Key Laboratory for Assisted Reproduction and Reproductive Genetics, Shanghai, People’s Republic of China

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Wang-sheng Wang Center for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People’s Republic of China
Shanghai Key Laboratory for Assisted Reproduction and Reproductive Genetics, Shanghai, People’s Republic of China

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Yi-kai Lin Center for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People’s Republic of China
Shanghai Key Laboratory for Assisted Reproduction and Reproductive Genetics, Shanghai, People’s Republic of China

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Jiang-wen Lu Center for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People’s Republic of China
Shanghai Key Laboratory for Assisted Reproduction and Reproductive Genetics, Shanghai, People’s Republic of China

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Wen-jiao Li Center for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People’s Republic of China
Shanghai Key Laboratory for Assisted Reproduction and Reproductive Genetics, Shanghai, People’s Republic of China

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Chu-yue Zhang Center for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People’s Republic of China
Shanghai Key Laboratory for Assisted Reproduction and Reproductive Genetics, Shanghai, People’s Republic of China

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Kang Sun Center for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People’s Republic of China
Shanghai Key Laboratory for Assisted Reproduction and Reproductive Genetics, Shanghai, People’s Republic of China

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parturition. The signal transducer and activator of transcription 3 (STAT3) is a transcription factor, which can be activated upon phosphorylation at Tyr 705 ( Darnell 1997 ). In silico analysis of the SAA1 gene reveals putative STAT3-binding sites in

Article Type:
Research Article
DOI:
https://doi.org/10.1530/JME-18-0263
Volume/Issue:
Volume 62: Issue 4
Free access