The ISWI family of ATP-dependent chromatin remodelers represses transcription by changing nucleosome positions. ISWI regulates nucleosome positioning by requiring a minimal length of extranucleosomal DNA for moving nucleosomes. ISW2 from Saccharomyces cerevisiae, a member of the ISWI family, has a conserved domain called SLIDE (SANT-like ISWI domain) that binds to extranucleosomal DNA ~19 base pairs from the edge of nucleosomes. Loss of SLIDE binding does not perturb binding of the ATPase domain or the initial movement of DNA inside of nucleosomes. Not only is extranucleosomal DNA required to help recruit ISW2, but also the interactions of the SLIDE domain with extranucleosomal DNA are functionally required to move nucleosomes
An ATP-dependent DNA translocase domain consisting of seven conserved motifs is a general feature of...
An ATP-dependent DNA translocase domain con-sisting of seven conserved motifs is a general feature o...
ATP-dependent nucleosome remodelers influence genetic processes by altering nucleosome occupancy, po...
The ISWI family of ATP-dependent chromatin remodelers represses transcription by changing nucleosome...
The ISWI family of ATP-dependent chromatin remodelers represses transcription by changing nucleosome...
Chromatin remodelers utilize the energy derived from ATP hydrolysis to mobilize nucleosomes. ISWI re...
Regulation of chromatin structures in eukaryotes involves ATP-dependent chromatin remodeler complexe...
The ISWI family of ATP-dependent chromatin remodelers represses transcription by changing nucleosome...
ISWI type remodelers mobilize and space nucleosomes. These ATP-dependent remodeling complexes have ...
ATP-dependent chromatin remodeling has an important role in the regulation of cellular differentiati...
ISWI proteins form the catalytic core of a subset of ATP-dependent chromatin remodeling activities i...
Members of the ISWI family of chromatin remodeling factors hydrolyze ATP to reposition nucleosomes a...
Chromatin remodeling complexes (CRCs) mobilize nucleosomes to mediate the access of DNA-binding fact...
ATP dependent Chromatin Remodelers hydrolyze ATP in order to move DNA around nucleosomes. ISWI famil...
The SANT domain is a nucleosome recognition module found in transcriptional regulatory proteins, inc...
An ATP-dependent DNA translocase domain consisting of seven conserved motifs is a general feature of...
An ATP-dependent DNA translocase domain con-sisting of seven conserved motifs is a general feature o...
ATP-dependent nucleosome remodelers influence genetic processes by altering nucleosome occupancy, po...
The ISWI family of ATP-dependent chromatin remodelers represses transcription by changing nucleosome...
The ISWI family of ATP-dependent chromatin remodelers represses transcription by changing nucleosome...
Chromatin remodelers utilize the energy derived from ATP hydrolysis to mobilize nucleosomes. ISWI re...
Regulation of chromatin structures in eukaryotes involves ATP-dependent chromatin remodeler complexe...
The ISWI family of ATP-dependent chromatin remodelers represses transcription by changing nucleosome...
ISWI type remodelers mobilize and space nucleosomes. These ATP-dependent remodeling complexes have ...
ATP-dependent chromatin remodeling has an important role in the regulation of cellular differentiati...
ISWI proteins form the catalytic core of a subset of ATP-dependent chromatin remodeling activities i...
Members of the ISWI family of chromatin remodeling factors hydrolyze ATP to reposition nucleosomes a...
Chromatin remodeling complexes (CRCs) mobilize nucleosomes to mediate the access of DNA-binding fact...
ATP dependent Chromatin Remodelers hydrolyze ATP in order to move DNA around nucleosomes. ISWI famil...
The SANT domain is a nucleosome recognition module found in transcriptional regulatory proteins, inc...
An ATP-dependent DNA translocase domain consisting of seven conserved motifs is a general feature of...
An ATP-dependent DNA translocase domain con-sisting of seven conserved motifs is a general feature o...
ATP-dependent nucleosome remodelers influence genetic processes by altering nucleosome occupancy, po...