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Title

High Transcript Level of Fatty Acid-Binding Protein 11 but Not of Very Low-Density Lipoprotein Receptor Is Correlated to Ovarian Follicle Atresia in a Teleost Fish (Solea senegalensis)

AuthorsAgulleiro Gozalbo, Maria Josep ; André, Michèle; Morais, Sofia; Cerdà, Joan ; Babin, Patrick J.
KeywordsFollicular development
Gametogenesis
Gene regulation
Oocyte development
Ovary
Issue Date2007
PublisherSociety for the Study of Reproduction
CitationBiology of Reproduction 77, 504–516 (2007)
AbstractTranscripts encoding a fatty acid-binding protein (FABP), Fabp11, and two isoforms of very low-density lipoprotein receptor (Vldlr; vitellogenin receptor) were characterized from the ovary of Senegalese sole (Solea senegalensis). Phylogenetic analyses of vertebrate FABPs demonstrated that Senegalese sole Fabp11, as zebrafish (Danio rerio) homologous sequences, is part of a newly defined teleost fish FABP subfamily that is a sister clade of tetrapod FABP4/FABP5/FABP8/FABP9. RT-PCR revealed high levels of vldlr transcript splicing variants in the ovaries and, to a lesser extent, in somatic tissues, whereas fabp11 was highly expressed in the ovaries, liver, and adipose tissue. In situ hybridization analysis showed vldlr and fabp11 mRNAs in previtellogenic oocytes, whereas no hybridization signals were detected in the larger vitellogenic oocytes. Transcript expression of fabp11 was strongly upregulated in somatic cells surrounding atretic follicles. Real-time quantitative RT-PCR demonstrated that ovarian transcript levels of vldlr and fabp11 had a significant positive correlation with the percentage of follicles in previtellogenesis and atresia, respectively. These results suggest that the expression level of vldlr transcripts may be used as a precocious functional marker to quantify the number of oocytes recruited for vitellogenesis and that fabp11 mRNA may be a very useful molecular marker for determining cellular events and environmental factors that regulate follicular atresia in fish.
Description13 pages, 8 figures
Publisher version (URL)http://dx.doi.org/10.1095/biolreprod.107.061598
URIhttp://hdl.handle.net/10261/20856
DOI10.1095/biolreprod.107.061598
ISSN0006-3363
Appears in Collections:(ICM) Artículos
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