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Regulation of promoter occupancy during activation of cryptobiotic embryos from the crustacean Artemia franciscana
Instituto de Investigaciones Biomédicas CSIC/UAM, C/ Arturo Duperier No. 4, 28029 Madrid, Spain
* Author for correspondence (e-mail: lsastre{at}iib.uam.es)
Accepted 10 February 2003
Artemia franciscana embryos can suspend their development and
metabolism at the gastrula stage to enter a state of cryptobiosis, forming
cysts. Embryonic development and metabolism can be resumed under favorable
environmental conditions to give rise to free-swimming larvae or nauplii. The
mechanisms that mediate these processes are not completely known. Here, we
report our studies of the mechanisms that regulate transcriptional activation
upon exiting cryptobiosis. Regulatory regions of several A.
franciscana gene promoters were identified. Functional analyses in
mammalian cells allowed the identification of transcriptional activator
regions in the Actin302 promoter and in promoter 2 of the
sarco/endoplasmic reticulum Ca2+-ATPase-encoding gene. These
regions were shown to specifically bind protein factors from nuclear extracts
of A. franciscana nauplii by means of electrophoretic mobility shift
assays. Several protein-binding regions were also detected by DNase I
protection analysis in the promoters of the genes encoding the
1
subunit of Na+/K+-ATPase, actin 302 and
sarco/endoplasmic reticulum Ca2+-ATPase. Specific DNA-binding
proteins in nauplius nuclear extracts were detected for all the promoter
regions analyzed. These proteins were either not present in cyst nuclear
extracts or were present in much smaller concentrations. Three of the five
regions analyzed also bound proteins present in cyst nuclear extracts. These
data indicate that transcriptional activation upon exiting cryptobiosis in
A. franciscana involves the expression/activation of DNA-binding
transcription factors that are not present in cyst nuclei
Key words: actin, Artemia franciscana, Ca2+-ATPase, cryptobiosis, development, gene expression, Na+/K+-ATPase, promoter, transcription