How Proteins Recognize the TATA Box
The crystal structure of a complex of human TATA-binding protein with TATA-sequence DNA has been solved, complementing earlier TBP/DNA analyses from Saccharomyces cerevisiaeand Arabidopsis thaliana. Special insight into TATA box specificity is provided by considering the TBP/DNA complex, not as a pr...
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Veröffentlicht in: | Journal of molecular biology 1996-08, Vol.261 (2), p.239-254 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The crystal structure of a complex of human TATA-binding protein with TATA-sequence DNA has been solved, complementing earlier TBP/DNA analyses from
Saccharomyces cerevisiaeand
Arabidopsis thaliana. Special insight into TATA box specificity is provided by considering the TBP/DNA complex, not as a protein molecule with bound DNA, but as a DNA duplex with a particularly large minor groove ligand. This point of view provides explanations for: (1) why T·A base-pairs are required rather than C·G; (2) why an alternation of T and A bases is needed; (3) how TBP recognizes the upstream and downstream ends of the TATA box in order to bind properly; and (4) why the second half of the TATA box can be more variable than the first. |
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ISSN: | 0022-2836 1089-8638 |
DOI: | 10.1006/jmbi.1996.0456 |