TY - JOUR
T1 - Histone chaperone FACT action during transcription through chromatin by RNA polymerase II
AU - Hsieh, Fu Kai
AU - Kulaeva, Olga I.
AU - Patel, Smita S.
AU - Dyer, Pamela N.
AU - Luger, Karolin
AU - Reinberg, Danny
AU - Studitsky, Vasily M.
PY - 2013/4/7
Y1 - 2013/4/7
N2 - FACT (facilitates chromatin transcription) is a histone chaperone that promotes chromatin recovery during transcription, with additional roles in cell differentiation. Although several models of the action of FACT during transcription have been proposed, they remain to be experimentally evaluated. Here we show that human FACT (hFACT) facilitates transcription through chromatin and promotes nucleosome recovery in vitro. FACT action depends on the presence of histone H2A/H2B dimers in the nucleosome. Kinetic analysis suggests that hFACT decreases the lifetime of nonproductive RNA polymerase II (Pol II)-nucleosome complexes and facilitates the formation of productive complexes containing nucleosomal DNA partially uncoiled from the octamer. Taken together, our data suggest that hFACT interacts with DNA-binding surfaces of H2A/H2B dimers, facilitating uncoiling of DNA from the histone octamer. Thus, hFACT-H2A/ H2B interactions play a key role in overcoming the nucleosomal barrier by Pol II and promoting nucleosome survival during transcription.
AB - FACT (facilitates chromatin transcription) is a histone chaperone that promotes chromatin recovery during transcription, with additional roles in cell differentiation. Although several models of the action of FACT during transcription have been proposed, they remain to be experimentally evaluated. Here we show that human FACT (hFACT) facilitates transcription through chromatin and promotes nucleosome recovery in vitro. FACT action depends on the presence of histone H2A/H2B dimers in the nucleosome. Kinetic analysis suggests that hFACT decreases the lifetime of nonproductive RNA polymerase II (Pol II)-nucleosome complexes and facilitates the formation of productive complexes containing nucleosomal DNA partially uncoiled from the octamer. Taken together, our data suggest that hFACT interacts with DNA-binding surfaces of H2A/H2B dimers, facilitating uncoiling of DNA from the histone octamer. Thus, hFACT-H2A/ H2B interactions play a key role in overcoming the nucleosomal barrier by Pol II and promoting nucleosome survival during transcription.
KW - Chromatin/chemistry
KW - Cross-Linking Reagents
KW - DNA-Binding Proteins/metabolism
KW - DNA/chemistry
KW - Dimerization
KW - Gene Expression Regulation
KW - High Mobility Group Proteins/metabolism
KW - Histones/metabolism
KW - Humans
KW - Models, Molecular
KW - Mutation
KW - Nucleosomes/metabolism
KW - RNA Polymerase II/metabolism
KW - Transcription, Genetic
KW - Transcriptional Elongation Factors/metabolism
UR - http://www.scopus.com/inward/record.url?scp=84877322380&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:000319327700040&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.1073/pnas.1222198110
DO - 10.1073/pnas.1222198110
M3 - Article
C2 - 23610384
SN - 0027-8424
VL - 110
SP - 7654
EP - 7659
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 19
ER -