Conference Paper
Transcriptome analyses and 3d geometric morphometrics characterization of lacustrine species pairs in Astyanax genus
Ornelas-Garcia, C.P., Powers, A., Berning, D., Rodiles, R., Barluenga, M. and Gross, J.B.
Record Number:
3261
Year:
2017
Journal:
AIM 2017
Abstract:
Independent lineages of lacustrine Astyanax species have shown convergent morphologies mainly
associated with trophic habits differences. Those differences between lacustrine species
corresponded to both body and trophic related traits. Despites the morphological differences,
which have made taxonomist to identified the different lacustrine forms as different genera (e.g.
Astyanax and Bramocharax), there is not a clear correspondence between genetic structure and
morphological divergence. Partial gene flow analyses, have shown a lack of prezygotic barriers
among divergent morphotypes. Based on the previously exposed problematic, the main goal of the
present stifle was to characterized the morphological variation among lacustrine morphs, using
Micro CT- Scans, in order to characterize the major osteological differences among lacustrine
forms and evaluate at this scale convergent patterns of morphological evolution, the previous
analyses were based on Geometric Morphometrics data of four lineages of Astyanax (Catemaco
Lake, Metzabook, Managua Lake and Lake Nicaragua). We also carried out a RNA-seq analysis,
in order to identify differences in expression levels of alternative phenotypes in the four lacustrine
systems within the Astyanax genus, in the Illumina platform. Based on the MANOVA carried out
with the geometric morphometric data, we found significant effect of both species and lakes
(P<0.05). For the RNA-Seq analyses, we identify a correlation index between divergent lacustrine
morphs of 0.83%. Among the most differentiated genes, we found 47 related to metabolic aspects.
The genes that presented the highest differences in the expression levels were: Craniofacial protein
1, CD74, preproinsuline, galactose – 3 – O – Sulfotransferase 1b and acetyl-CoA carboxilase.
Times Cited:
1
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