Literature DB >> 8604337

The DNA bend angle and binding affinity of an HMG box increased by the presence of short terminal arms.

M Lnenicek-Allen1, C M Read, C Crane-Robinson.   

Abstract

The HMG box of human LEF-1 (hLEF-1, formerly TCF1alpha) has been expressed in four forms: a parent box of 81 amino acids and constructs having either a 10 amino acid C-terminal extension, a 9 amino acid N-terminal extension, or both. These four species have been compared for DNA binding and bending ability using a 28 bp recognition sequence from the TCR alpha-chain enhancer. In the bending assay, whereas the parent box and that with the N-terminal extension bent the DNA by 57/58 degrees, the box extended at the C-terminus bent the DNA by 77/78 degrees, irrespective of the presence or absence of the N-terminal extension. A 6- fold increase in DNA affinity also resulted from addition of both terminal extensions. These observations redefine the functional boundaries of the HMG box. The structure of a mouse LEF-1/DNA complex recently published [Love et al. (1995) Nature 376, 791-795] implies that the higher DNA affinity and in particular the increased bend angle observed are consequences, at least in part, of the C-terminal extension spanning the major groove on the inside of the DNA bend.

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Year:  1996        PMID: 8604337      PMCID: PMC145749          DOI: 10.1093/nar/24.6.1047

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  35 in total

1.  A thymus-specific member of the HMG protein family regulates the human T cell receptor C alpha enhancer.

Authors:  M L Waterman; W H Fischer; K A Jones
Journal:  Genes Dev       Date:  1991-04       Impact factor: 11.361

2.  The HMG domain of lymphoid enhancer factor 1 bends DNA and facilitates assembly of functional nucleoprotein structures.

Authors:  K Giese; J Cox; R Grosschedl
Journal:  Cell       Date:  1992-04-03       Impact factor: 41.582

3.  DNA-binding properties of the HMG domain of the lymphoid-specific transcriptional regulator LEF-1.

Authors:  K Giese; A Amsterdam; R Grosschedl
Journal:  Genes Dev       Date:  1991-12       Impact factor: 11.361

4.  Solution structure of a DNA-binding domain from HMG1.

Authors:  C M Read; P D Cary; C Crane-Robinson; P C Driscoll; D G Norman
Journal:  Nucleic Acids Res       Date:  1993-07-25       Impact factor: 16.971

5.  The nonspecific DNA-binding and -bending proteins HMG1 and HMG2 promote the assembly of complex nucleoprotein structures.

Authors:  T T Paull; M J Haykinson; R C Johnson
Journal:  Genes Dev       Date:  1993-08       Impact factor: 11.361

6.  A high-mobility-group protein and its cDNAs from Drosophila melanogaster.

Authors:  C R Wagner; K Hamana; S C Elgin
Journal:  Mol Cell Biol       Date:  1992-05       Impact factor: 4.272

7.  LEF-1, a gene encoding a lymphoid-specific protein with an HMG domain, regulates T-cell receptor alpha enhancer function [corrected].

Authors:  A Travis; A Amsterdam; C Belanger; R Grosschedl
Journal:  Genes Dev       Date:  1991-05       Impact factor: 11.361

8.  SRY, like HMG1, recognizes sharp angles in DNA.

Authors:  S Ferrari; V R Harley; A Pontiggia; P N Goodfellow; R Lovell-Badge; M E Bianchi
Journal:  EMBO J       Date:  1992-12       Impact factor: 11.598

9.  The DNA binding site of HMG1 protein is composed of two similar segments (HMG boxes), both of which have counterparts in other eukaryotic regulatory proteins.

Authors:  M E Bianchi; L Falciola; S Ferrari; D M Lilley
Journal:  EMBO J       Date:  1992-03       Impact factor: 11.598

10.  Structure of the HMG box motif in the B-domain of HMG1.

Authors:  H M Weir; P J Kraulis; C S Hill; A R Raine; E D Laue; J O Thomas
Journal:  EMBO J       Date:  1993-04       Impact factor: 11.598

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  12 in total

Review 1.  Regulation of DNA-dependent activities by the functional motifs of the high-mobility-group chromosomal proteins.

Authors:  M Bustin
Journal:  Mol Cell Biol       Date:  1999-08       Impact factor: 4.272

2.  DNA looping in the RNA polymerase I enhancesome is the result of non-cooperative in-phase bending by two UBF molecules.

Authors:  V Y Stefanovsky; G Pelletier; D P Bazett-Jones; C Crane-Robinson; T Moss
Journal:  Nucleic Acids Res       Date:  2001-08-01       Impact factor: 16.971

Review 3.  Priming the nucleosome: a role for HMGB proteins?

Authors:  Andrew A Travers
Journal:  EMBO Rep       Date:  2003-02       Impact factor: 8.807

4.  Dual binding modes for an HMG domain from human HMGB2 on DNA.

Authors:  Micah McCauley; Philip R Hardwidge; L James Maher; Mark C Williams
Journal:  Biophys J       Date:  2005-04-15       Impact factor: 4.033

5.  Solution structure and backbone dynamics of the DNA-binding domain of mouse Sox-5.

Authors:  P D Cary; C M Read; B Davis; P C Driscoll; C Crane-Robinson
Journal:  Protein Sci       Date:  2001-01       Impact factor: 6.725

6.  Mutagenesis of the HMGB (high-mobility group B) protein Cmb1 (cytosine-mismatch binding 1) of Schizosaccharomyces pombe: effects on recognition of DNA mismatches and damage.

Authors:  Christophe Kunz; Karin Zurbriggen; Oliver Fleck
Journal:  Biochem J       Date:  2003-06-01       Impact factor: 3.857

7.  Biophysical characterizations of human mitochondrial transcription factor A and its binding to tumor suppressor p53.

Authors:  Tuck Seng Wong; Sridharan Rajagopalan; Stefan M Freund; Trevor J Rutherford; Antonina Andreeva; Fiona M Townsley; Miriana Petrovich; Alan R Fersht
Journal:  Nucleic Acids Res       Date:  2009-09-15       Impact factor: 16.971

8.  Deciphering the role of the AT-rich interaction domain and the HMG-box domain of ARID-HMG proteins of Arabidopsis thaliana.

Authors:  Adrita Roy; Arkajyoti Dutta; Dipan Roy; Payel Ganguly; Ritesh Ghosh; Rajiv K Kar; Anirban Bhunia; Jayanta Mukhopadhyay; Shubho Chaudhuri
Journal:  Plant Mol Biol       Date:  2016-08-09       Impact factor: 4.076

9.  The DNA binding and bending activities of truncated tail-less HMGB1 protein are differentially affected by Lys-2 and Lys-81 residues and their acetylation.

Authors:  Ivan Elenkov; Petar Pelovsky; Iva Ugrinova; Masayuki Takahashi; Evdokia Pasheva
Journal:  Int J Biol Sci       Date:  2011-06-01       Impact factor: 6.580

10.  High-mobility-group box nuclear factors of Plasmodium falciparum.

Authors:  Sylvie Briquet; Charlotte Boschet; Mathieu Gissot; Emilie Tissandié; Elisa Sevilla; Jean-François Franetich; Isabelle Thiery; Zuhal Hamid; Catherine Bourgouin; Catherine Vaquero
Journal:  Eukaryot Cell       Date:  2006-04
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