INVESTIGADORES
CAVIEDES VIDAL enrique juan raul
congresos y reuniones científicas
Título:
Ontogeny and dietary effect on gene expression of intestinal carbohydrases in birds with the altricial mode of development
Autor/es:
CAVIEDES VIDAL, E; GATICA-SOSA CP; BRZEK, P.; KARASOV WH
Lugar:
Salzburg
Reunión:
Encuentro; Annual Meeting of the Society for Experimental Biology; 2012
Institución organizadora:
Society for Experimental Biology
Resumen:
In birds, developmental changes in digestive enzymes occur during
transition from a lipid-rich yolk diet inside the egg to a carbohydrate- and
protein-based diet post hatching. Carbohydrase activity, which is critical
for starch digestion, increases per unit intestine under control of intrinsic
regulatory (?hard-wired?) mechanisms and, in some species, environmental
signals such as increased dietary starch (called dietary induction). We
predicted that in altricial birds such increases are paralleled by increases
in expression of genes, which is the case in mammals and chickens.
House sparrows and zebra finch nestlings were each raised on two
diets that differed in starch content. Seemingly hard-wired increases
in intestinal maltase and sucrase activity prior to fledging occurred in
the absence of significant increases in mRNA for enzymes maltaseglucoamylase and sucrase-isomaltase, in contrast to our prediction.
Carbohydrase activities were induced by dietary starch only in the house
sparrow, and increased activity was correlated with increased mRNA
for both maltase-glucoamylase and sucrase-isomaltase, suggesting
transcriptional control of the diet-induced response.
Post-fledging changes were then studied in house sparrows. Parallel
up and down changes in carbohydrase activities and mRNA were
inducible by dietary carbohydrate changes in house sparrow fledglings,
demonstrating reversible flexibility under apparent transcriptional control.
We conclude that in altricial birds ontogenetic changes in enzyme
activity are under the control of both transcriptional and post-transcriptional
mechanisms.
Supported by USA National Science Foundation IOS 0615678 and
1025886, and by Argentina PICT2007-01320 and UNSL CyT 4-9502