Literature DB >> 17097219

Distal regulatory elements are required for Fshr expression, in vivo.

Brian P Hermann1, Kaori I Hornbaker, Rengasamy R M Maran, Leslie L Heckert.   

Abstract

The gonadotropin follicle-stimulating hormone (FSH) is required for initiation and maintenance of normal gametogenesis and acts through a specific, cell-surface receptor (Fshr) present only on Sertoli and granulosa cells in the gonads. Despite extensive examination of the transcriptional mechanisms regulating Fshr, the sequences directing its expression to these cells remain unidentified. To establish the minimal region necessary for Fshr expression, we generated transgenic mice carrying a yeast artificial chromosome (YAC) that contained 413 kilobases (kb) of the rat Fshr locus (YAC60). Transgene expression, as determined by RT-PCR, was absent from immature testis and Sertoli cells, limited to germ cells of the adult testis, and never observed in the ovary. While the data is limited to only one transgenic line, it suggests that the 413kb region does not specify the normal spatiotemporal expression pattern of Fshr. Comparative genomics was used to identify potential distal regulatory elements, revealing seven regions of high evolutionary conservation (>80% identity over 100bp or more), six of which were absent from the transgene. Functional examination of the evolutionary conserved regions (ECRs) by transient transfection revealed that all of the ECRs had modest transcriptional activity in Sertoli or myoid cells with two, ECR4 and ECR5, showing differential effects in expressing and non-expressing cells. These data reveal that distal regulatory regions (outside the 413kb in YAC60) are required for appropriate temporal and spatial Fshr expression and implicate the identified ECRs in transcriptional regulation of Fshr.

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Year:  2006        PMID: 17097219      PMCID: PMC1764205          DOI: 10.1016/j.mce.2006.01.017

Source DB:  PubMed          Journal:  Mol Cell Endocrinol        ISSN: 0303-7207            Impact factor:   4.102


  41 in total

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2.  Silencing of Fshr occurs through a conserved, hypersensitive site in the first intron.

Authors:  Brian P Hermann; Leslie L Heckert
Journal:  Mol Endocrinol       Date:  2005-04-07

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Authors:  J Levallet; P Koskimies; N Rahman; I Huhtaniemi
Journal:  Mol Endocrinol       Date:  2001-01

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Authors:  Leslie L Heckert; Michael D Griswold
Journal:  Recent Prog Horm Res       Date:  2002

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  12 in total

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6.  In vivo regulation of follicle-stimulating hormone receptor by the transcription factors upstream stimulatory factor 1 and upstream stimulatory factor 2 is cell specific.

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7.  The regulatory repertoire of PLZF and SALL4 in undifferentiated spermatogonia.

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8.  GATA factors and androgen receptor collaborate to transcriptionally activate the Rhox5 homeobox gene in Sertoli cells.

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10.  Metformin inhibits follicle-stimulating hormone (FSH) action in human granulosa cells: relevance to polycystic ovary syndrome.

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