ATP-dependent structural change of the eukaryotic clamp-loader protein, replication factor C

Yasushi Shiomi, Jiro Usukura, Yusuke Masamura, Kunio Takeyasu, Yoshikazu Nakayama, Chikashi Obuse, Hiroshi Yoshikawa, Toshiki Tsurimoto

Research output: Contribution to journalArticlepeer-review

64 Citations (Scopus)

Abstract

The eukaryotic DNA sliding clamp that keeps DNA polymerase engaged at a replication fork, called proliferating cell nuclear antigen (PCNA), is loaded onto the 3′ ends of primer DNA through its interaction with a heteropentameric protein complex called replication factor C (RFC). The ATPase activity of RFC is necessary for formation of a functional PCNA clamp. In the present study, the sensitivity of RFC to partial proteolysis is used to show that addition of ATP, ATPγS, or ADP induces different structural changes in RFC. Direct observation by electron microscopy reveals that RFC has a closed two-finger structure called the U form in the absence of ATP. This is converted into a more open C form on addition of ATP. In contrast, the structural changes induced by ATPγS or ADP are limited. These results suggest that RFC adapts on opened configuration intermediately after ATP hydrolysis. We further observe that PCNA is held between the two fingers of RFC and propose that the RFC structure change we observe during ATP hydrolysis causes the attached PCNA to form its active ring-like clamp on DNA.

Original languageEnglish
Pages (from-to)14127-14132
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume97
Issue number26
DOIs
Publication statusPublished - Dec 19 2000

All Science Journal Classification (ASJC) codes

  • General

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