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Identification and characterization of cis elements in the STAT3 gene regulating STAT3α and STAT3β messenger RNA splicing
被引:39
|作者:
Shao, H
Quintero, AJ
Tweardy, DJ
机构:
[1] Baylor Coll Med, Infect Dis Sect, Dept Med, Houston, TX 77030 USA
[2] Univ Pittsburgh, Inst Canc, Pittsburgh, PA 15260 USA
来源:
关键词:
D O I:
10.1182/blood.V98.13.3853
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
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 STAT3 alpha, and STAT3 beta mRNA. (C) 2001 by The American Society of Hematology.
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页码:3853 / 3856
页数:4
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