Literature DB >> 18667423

Fusion of OTT to BSAC results in aberrant up-regulation of transcriptional activity.

Taisuke Sawada1, Chiharu Nishiyama, Takuma Kishi, Tomonari Sasazuki, Sachiko Komazawa-Sakon, Xin Xue, Jiang-Hu Piao, Hideko Ogata, Jun-ichi Nakayama, Tomohiko Taki, Yasuhide Hayashi, Mamoru Watanabe, Hideo Yagita, Ko Okumura, Hiroyasu Nakano.   

Abstract

OTT/RBM15-BSAC/MAL/MKL1/MRTF-A was identified as a fusion transcript generated by t(1;22)(p13;q13) in acute megakaryoblastic leukemia. Previous studies have shown that BSAC (basic, SAP, and coiled-coil domain) activates the promoters containing CArG boxes via interaction with serum response factor, and OTT (one twenty-two) negatively regulates the development of megakaryocytes and myeloid cells. However, the mechanism by which OTT-BSAC promotes leukemia is largely unknown. Here we show that OTT-BSAC, but not BSAC or OTT strongly activates several promoters containing a transcription factor Yin Yang 1-binding sequence. In addition, although BSAC predominantly localizes in the cytoplasm and its nuclear translocation is considered to be regulated by the Rho-actin signaling pathway, OTT-BSAC exclusively localizes in the nucleus. Moreover, OTT interacts with histone deacetylase 3, but this interaction is abolished in OTT-BSAC. Collectively, these functional and spatial changes of OTT and BSAC caused by the fusion might perturb their functions, culminating in the development of acute megakaryoblastic leukemia.

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Year:  2008        PMID: 18667423      PMCID: PMC3258922          DOI: 10.1074/jbc.M802315200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


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