Abstract
In embryonic neural retina the enzyme glutamine synthetase [GS; L-glutamate:ammonia ligase (ADP-forming), EC 6.3.1.2] is a glia-specific differentiation marker inducible with cortisol. We show that cortisol elicits GS mRNA accumulation by stimulating transcription of the GS gene and that this stimulation requires cell contacts: in dissociated and separated retina cells GS gene transcription was not induced; when the separated cells were reassembled into multicellular aggregates, restoring cell contacts, accumulation of GS mRNA was again inducible. In cells dissociated from retina tissue that had been preinduced with cortisol, GS gene transcription rapidly declined, despite continued hormone availability. In the separated cells transcription of the histone H3.3 gene and accumulation of carbonic anhydrase II mRNA were unaffected; therefore, cell separation selectively precluded induction of the GS gene. These findings provide direct evidence for the regulatory role of cell contacts in hormonal control of gene transcription.
MeSH Terms
Animals
Cell Aggregation
Cell Communication
Chick Embryo
Glutamate-Ammonia Ligase/genetics
Hydrocortisone/pharmacology
RNA, Messenger/analysis
Retina/enzymology
Transcription, Genetic/drug effects
Chemicals
RNA, Messenger
Glutamate-Ammonia Ligase
Hydrocortisone
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Vardimon L
Department of Molecular Genetics and Cell Biology, University of Chicago, IL 60637.
Fox L L
Degenstein L
Moscona A A
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