Follicular expression of follicle stimulating hormone receptor variants in the ewe

dc.citation.doidoi:10.1186/1477-7827-11-113en_US
dc.citation.issue1en_US
dc.citation.jtitleReproductive Biology and Endocrinologyen_US
dc.citation.spage113en_US
dc.citation.volume11en_US
dc.contributor.authorSullivan, Rachael R.
dc.contributor.authorFaris, Brian R.
dc.contributor.authorEborn, Douglas
dc.contributor.authorGrieger, David M.
dc.contributor.authorCino-Ozuna, Ada G.
dc.contributor.authorRozell, Timothy G.
dc.contributor.authoreidrachworken_US
dc.contributor.authoreidbrfarisen_US
dc.contributor.authoreiddgriegeren_US
dc.contributor.authoreidtrozellen_US
dc.contributor.authoreidgcino
dc.date.accessioned2014-02-25T21:14:55Z
dc.date.available2014-02-25T21:14:55Z
dc.date.issued2014-02-25
dc.date.published2013en_US
dc.description.abstractBackground: Several alternatively-spliced mRNA transcripts of the follicle stimulating hormone receptor (FSHR) have been identified in sheep, including FSHR-1 (G protein-coupled form), FSHR-2 (dominant negative form), and FSHR-3 (growth factor type-1 form). Our objective was to determine which of these variants is predominantly expressed in follicles collected from ewes at various times after estrus. Methods: Suffolk-cross ewes (n = 8) were allowed to come into estrus naturally and were euthanized 24 (n = 3), 36 (n = 3), or 48 (n = 2) hours after the onset of estrus. All visible follicles were measured, aspirated and pooled according to follicular diameter: small (<= 2.0 mm), medium (2.1-4.0 mm), large (4.1-6.0 mm), and preovulatory (> = 6.1 mm). Aspirated cells were separated from follicular fluid by centrifugation. Total RNA was extracted from cell pellets and reverse transcribed. The resulting cDNA was subjected to qPCR, using primer sets designed to amplify each variant specifically. Gene expression was normalized to that of beta–actin within samples, and compared by analysis of variance with the level of significant differences set at p < .05. Results: Relative expression of FSHR-3 exceeded that of both FSHR-1 and FSHR-2 in medium follicles, and tended to be higher in small follicles (p = .09) regardless of time after onset of estrus, and thus results from different time points were pooled. Expression of FSHR-3 was greater than that of FSHR-2 and luteinizing hormone receptor (LHR) in small and medium follicles. Expression of LHR was greatest in preovulatory follicles. Conclusions: These experiments show that in addition to the well characterized G protein-coupled form of the FSHR, alternatively spliced variants of the FSHR may participate in follicular dynamics during follicular waves of the sheep estrous cycle. Furthermore, these results indicate that an “alternatively” spliced form of the FSHR (FSHR-3) is the predominant form of the FSHR in the sheep.en_US
dc.identifier.urihttp://hdl.handle.net/2097/17186
dc.language.isoen_USen_US
dc.relation.urihttp://www.rbej.com/content/11/1/113en_US
dc.subjectFSH receptoren_US
dc.subjectFollicle developmenten_US
dc.subjectEween_US
dc.subjectCIDRen_US
dc.subjectAlternate splicingen_US
dc.titleFollicular expression of follicle stimulating hormone receptor variants in the eween_US
dc.typeArticle (publisher version)en_US

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