Nuclear import of the TATA-binding protein: Mediation by the karyopherin Kap114p and a possible mechanism for intranuclear targeting

被引:103
作者
Pemberton, LF [1 ]
Rosenblum, JS [1 ]
Blobel, G [1 ]
机构
[1] Rockefeller Univ, Cell Biol Lab, Howard Hughes Med Inst, New York, NY 10021 USA
关键词
biological transport; transcription factors; nuclear localization signal; Saccharomyces cerevisiae;
D O I
10.1083/jcb.145.7.1407
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Binding of the TATA-binding protein (TBP) to the promoter is the first and rate limiting step in the formation of transcriptional complexes, We show here that nuclear import of TBP is mediated by a new karyopherin (Kap) (importin) family member, Kap114p. Kap114p is localized to the cytoplasm and nucleus. A complex of Kap114p and TBP was detected in the cytosol and could be reconstituted using recombinant proteins, suggesting that the interaction was direct. Deletion of the KAP114 gene led to specific mislocalization of TBP to the cytoplasm. We also describe two other potential minor import pathways for TBP. Consistent with other Kaps, the dissociation of TBP from Kap114p is dependent on RanGTP. However, we could show that double stranded, TATA-containing DNA stimulates this RanGTP-mediated dissociation of TBP, and is necessary at lower RanGTP concentrations. This suggests a mechanism where, once in the nucleus, TBP is preferentially released from Kap114p at the promoter of genes to be transcribed. In this fashion Kap114p may play a role in the intranuclear targeting of TBP.
引用
收藏
页码:1407 / 1417
页数:11
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