Literature DB >> 11867548

The structure of the Dead ringer-DNA complex reveals how AT-rich interaction domains (ARIDs) recognize DNA.

Junji Iwahara1, Mizuho Iwahara, Gary W Daughdrill, Joseph Ford, Robert T Clubb.   

Abstract

The AT-rich interaction domain (ARID) is a DNA-binding module found in many eukaryotic transcription factors. Using NMR spectroscopy, we have determined the first ever three-dimensional structure of an ARID--DNA complex (mol. wt 25.7 kDa) formed by Dead ringer from Drosophila melanogaster. ARIDs recognize DNA through a novel mechanism involving major groove immobilization of a large loop that connects the helices of a non-canonical helix-turn-helix motif, and through a concomitant structural rearrangement that produces stabilizing contacts from a beta-hairpin. Dead ringer's preference for AT-rich DNA originates from three positions within the ARID fold that form energetically significant contacts to an adenine-thymine base step. Amino acids that dictate binding specificity are not highly conserved, suggesting that ARIDs will bind to a range of nucleotide sequences. Extended ARIDs, found in several sequence-specific transcription factors, are distinguished by the presence of a C-terminal helix that may increase their intrinsic affinity for DNA. The prevalence of serine amino acids at all specificity determining positions suggests that ARIDs within SWI/SNF-related complexes will interact with DNA non-sequence specifically.

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Year:  2002        PMID: 11867548      PMCID: PMC125891          DOI: 10.1093/emboj/21.5.1197

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  65 in total

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4.  Characterization of the dead ringer gene identifies a novel, highly conserved family of sequence-specific DNA-binding proteins.

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Journal:  Mol Cell Biol       Date:  1996-03       Impact factor: 4.272

5.  Protein backbone angle restraints from searching a database for chemical shift and sequence homology.

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Authors:  M Vázquez; L Moore; J A Kennison
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  25 in total

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2.  Preparation and optimization of protein-DNA complexes suitable for detailed NMR studies.

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Journal:  Methods Mol Biol       Date:  2012

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6.  Compensating increases in protein backbone flexibility occur when the Dead ringer AT-rich interaction domain (ARID) binds DNA: a nitrogen-15 relaxation study.

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8.  Structural basis of DNA recognition by the alternative sigma-factor, sigma54.

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Review 9.  Plant proteins containing high mobility group box DNA-binding domains modulate different nuclear processes.

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