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ARS Home » Southeast Area » Stoneville, Mississippi » Warmwater Aquaculture Research Unit » Research » Publications at this Location » Publication #297744
Title: Transcriptional regulation of teleost aicda genes. Pt 1 suppressors of promiscuous promoters

Author
item VOLLOTA-HERDOIZA, D. - University Of Alberta
item PILA, E - University Of Alberta
item Quiniou, Sylvie
item Waldbieser, Geoffrey - Geoff
item MAGOR, B - University Of Alberta

Submitted to: Fish and Shellfish Immunology
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: 9/30/2013
Publication Date: 10/24/2013
Citation: Vollota-Herdoiza, D., Pila, E.A., Quiniou, S., Waldbieser, G.C., Magor, B. 2013. Transcriptional regulation of teleost aicda genes. Pt 1 suppressors of promiscuous promoters. Fish and Shellfish Immunology. 35(6):1981-1987.

Interpretive Summary: Cooperative research between scientists at the USDA, ARS, Warmwater Aquaculture Research Unit and the University of Alberta led to the production of gene constructs for investigations into the mechanisms of regulation of the Activation- Induced Cytidine Deaminase (AID) gene. Gene constructs that contained the basal regulatory regions of the gene were active in cells that do not normally express this gene, but when additional regions of the gene were added to the gene construct, gene activity was suppressed. This research provided basic information regarding gene control and regulation in catfish cells.

Technical Abstract: In order to better understand antibody affinity maturation in fishes we sought to identify gene regulatory elements that could drive expression of activated B-cell specific fluorescent reporter transgenes in zebrafish. Specifically the promoter and several non-coding regions of the channel catfish (Ictalurus punctatus) and zebrafish (Danio rerio) were tested for transcriptional activity using a dual luciferase reporter system in transfected fish leukocytes and two mammalian cell lines that constitutively express Aicda. The promoters of both fish Aicda genes were as transcriptionally active as an SV40 promoter control in all cell lines tested, regardless of the cells ability to express Aicda. Coupling of a putative intron 1 enhancer or a region 10 kb upstream of the zebrafish promoter effectively silenced transcription from the fish Aicda promoter. Paradoxically these suppressor elements enhanced transcription when they were coupled to the mouse Aicda intron 1 enhancer. The results are considered in context of similar observations for Aicda transcriptional regulation in mice and in light of recent evidence that Aicda is utilized for epigenetic reprograming of several non-lymphoid cell types.