Molecular
markers of oocyte differentiation in European eel during hormonally induced
oogenesis
I. Rojo-Bartolomé, L. Martínez-Miguel, A.G. Lafont, M.C. Vílchez, J.F. Asturiano, L. Pérez, I. Cancio
Abstract
I. Rojo-Bartolomé, L. Martínez-Miguel, A.G. Lafont, M.C. Vílchez, J.F. Asturiano, L. Pérez, I. Cancio
Abstract
Reproduction in
captivity is a key study issue in Anguilla
anguilla as a possible solution for its dwindling population. Understanding
the mechanisms controlling the production of ribosomal building blocks during
artificially induced oocyte maturation could be particularly interesting.
Transcription levels of ribosomal biogenesis associated genes could be used as
markers to monitor oogenesis. Eels from the Albufera Lagoon were injected with
carp pituitary extract for 15 weeks and ovaries in previtellogenic (PV) stage
(non-injected), in early-, mid-, late-vitellogenesis (EV, MV, LV), as well as
in nuclear migration migratory nucleus stage (NMN) were analysed. 5S rRNA and
related genes were highly transcribed in ovaries with PV oocytes. As oocytes
developed, transcriptional levels of genes related to 5S rRNA production
(gtf3a), accumulation (gtf3a, 42sp43) and nucleocytoplasmic transport (rpl5,
rpl11) and the 5S/18S rRNA index decreased (PV>EV>MV>LV>MN). On the
contrary, 18S rRNA was at its highest at MN stage while ubtf1 in charge of
activating RNA-polymerase I and synthesising 18S rRNA behaved as 5S related
genes. Individuals that did not respond (NR) to the treatment showed 5S/18S
index values similar to PV females, while studied genes showed EV/LV-like
transcription levels. Therefore, NR females fail to express the largest rRNAs,
which could thus be taken as markers of successful vitellogenesis progression.
In conclusion, we have proved that the transcriptional dynamics of ribosomal
genes provides useful tools to characterize induced ovarian development in
European eels. In the future, such markers should be studied as putative
indicators of response to hormonal treatments and of the quality of obtained
eel oocytes.
Doi: 10.1016/j.cbpa.2017.05.018
Available here: http://www.sciencedirect.com/science/article/pii/S1095643317301216
Doi: 10.1016/j.cbpa.2017.05.018
Available here: http://www.sciencedirect.com/science/article/pii/S1095643317301216
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