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Nucleic Acids Research, 1992, Vol. 20, No. 16 4187-4192
© 1992


MOLECULAR BIOLOGY

Isolation and characterization of the chicken bcl–2 gene: expression in a variety of tissues including lymphoid and neuronal organs in adult and embryo

Yutaka Eguchi+, Donald L. Ewert and Yoshihide Tsujimoto*,+

The Wistar Institute of Anatomy and Biology 36th Street at Spruce, Philadelphia, PA 19104, USA

*To whom correspondence should be addressed

Received June 3, 1992. Revised July 17, 1992. Accepted July 17, 1992.

The expression of human bcl–2 gene is de-regulated by t(14;18) translocatlon in most of follicular lymphoma. Recent studies indicated that the bcl–2 gene product has an ability to block apoptosis of nematopoletic cells. To facilitate the analysis of the role of this gene in normal development using an animal model, we have isolated and partially characterized the chicken homologue of human bcl–2 gene. The analysis of nucleotlde sequence showed that the organization of the chicken bcl–2 gene is very similar to that of human bcl–2 gene. The primary transcript is spliced to encode a 25,687 dalton (233 a.a.) protein. The chicken bcl–2 protein has two regions highly homologous to human bcl–2 protein surrounding a totally non-homologous region. The expression of the chicken bcl–2 gene was analyzed in various chicken tissues. In the adult chicken, bcl–2 transcripts were detected in thymus, spleen, kidney, heart, ovary and brain, with the highest levels being detected In the thymus. However, the bursa of Fabriclus, which is the site of early B cell development, expressed much less amounts of bcl–2 RNA. On the other hand, in embryo, the gene is extensively expressed in the bursa, as well as in muscle and the above tissues. Our findings indicate that a homologue of the human bcl–2 gene does exist in the chicken and that its expression Is developmentally regulated in some tissues.


+Present address: Biomedical Research Center, Osaka University Medical School, 2–2 Yamadaoka, Suita, Osaka 565, Japan


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