spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Martinez-Lamparero, A.
Right arrow Articles by Sastre, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Martinez-Lamparero, A.
Right arrow Articles by Sastre, L.
The Journal of Experimental Biology 206, 1565-1573 (2003)
doi: 10.1242/jeb.00285

Regulation of promoter occupancy during activation of cryptobiotic embryos from the crustacean Artemia franciscana

Ana Martinez-Lamparero, Marie-Carmen Casero, Javier Ortiz-Caro and Leandro Sastre*

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 {alpha}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







© The Company of Biologists Ltd 2003