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Blood, 15 December 2001, Vol. 98, No. 13, pp. 3853-3856

BRIEF REPORT

Identification and characterization of cis elements in the STAT3 gene regulating STAT3alpha and STAT3beta messenger RNA splicing

Huang Shao, Andres J. Quintero, and David J. Tweardy

From the Section of Infectious Diseases, Department of Medicine, Baylor College of Medicine, Houston, TX; and the University of Pittsburgh Cancer Institute, PA.

Signal transducer and activator of transcription 3 (STAT3) is an oncogene and a critical regulator of multiple cell-fate decisions, including myeloid cell differentiation. Two isoforms of STAT3 have been identified: alpha  (p92) and beta  (p83). These differ structurally in their C-terminal transactivation domains, resulting in distinct functional activities. The cis genetic elements that regulate the ratio of alpha  to beta  messenger RNA (mRNA) are unknown. In this study, cloning, sequencing, and splicing analysis of the human and murine STAT3 genes revealed a highly conserved 5' donor site for generation of both alpha  and beta  mRNA and distinct branch-point sequences, polypyrimidine tracts, and 3' acceptor sites (ASs) for each. The beta  3' AS was found to be located 50 nucleotides downstream of the alpha  3' AS in exon 23. Two additional cryptic 3' ASs (delta  and epsilon ) were also identified. Thus, we identified for the first time the cis regulatory sequences responsible for generation of STAT3alpha and STAT3beta mRNA.

© 2001 by The American Society of Hematology.
 

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