DNA-binding properties of ARID family proteins
AUTOR(ES)
Patsialou, Antonia
FONTE
Oxford University Press
RESUMO
The ARID (A–T Rich Interaction Domain) is a helix–turn–helix motif-based DNA-binding domain, conserved in all eukaryotes and diagnostic of a family that includes 15 distinct human proteins with important roles in development, tissue-specific gene expression and proliferation control. The 15 human ARID family proteins can be divided into seven subfamilies based on the degree of sequence identity between individual members. Most ARID family members have not been characterized with respect to their DNA-binding behavior, but it is already apparent that not all ARIDs conform to the pattern of binding AT-rich sequences. To understand better the divergent characteristics of the ARID proteins, we undertook a survey of DNA-binding properties across the entire ARID family. The results indicate that the majority of ARID subfamilies (i.e. five out of seven) bind DNA without obvious sequence preference. DNA-binding affinity also varies somewhat between subfamilies. Site-specific mutagenesis does not support suggestions made from structure analysis that specific amino acids in Loop 2 or Helix 5 are the main determinants of sequence specificity. Most probably, this is determined by multiple interacting differences across the entire ARID structure.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=546134Documentos Relacionados
- Multivalent DNA-binding properties of the HMG-1 proteins.
- Rapid isolation of specific DNA-binding proteins and their DNA-binding domains.
- Using electrostatic potentials to predict DNA-binding sites on DNA-binding proteins
- DNA-binding activity of papillomavirus proteins.
- The DNA-binding properties of the ARID-containing subunits of yeast and mammalian SWI/SNF complexes