Abstract

Ordered nucleosome disassembly and reassembly are required for eukaryotic DNA replication. The facilitates chromatin transcription (FACT) complex, a histone chaperone comprising Spt16 and SSRP1, is involved in DNA replication as well as transcription. FACT associates with the MCM helicase, which is involved in DNA replication initiation and elongation. Although the FACT-MCM complex is reported to regulate DNA replication initiation, its functional role in DNA replication elongation remains elusive. To elucidate the functional role of FACT in replication fork progression during DNA elongation in the cells, we generated and analyzed conditional SSRP1 gene knock-out chicken (Gallus gallus) DT40 cells. SSRP1-depleted cells ceased to grow and exhibited a delay in S-phase cell cycle progression, although SSRP1 depletion did not affect the level of chromatin-bound DNA polymerase α or nucleosome reassembly on daughter strands. The tracking length of newly synthesized DNA, but not origin firing, was reduced in SSRP1-depleted cells, suggesting that the S-phase cell cycle delay is mainly due to the inhibition of replication fork progression rather than to defects in the initiation of DNA replication in these cells. We discuss the mechanisms of how FACT promotes replication fork progression in the cells.

Highlights

  • Ordered nucleosome disassembly and reassembly are required for eukaryotic DNA replication

  • A pioneering study using Xenopus egg extracts in a cellular DNA replication system showed that the histone chaperone facilitates chromatin transcription (FACT) is required for DNA replication [29]

  • To further elucidate the functional roles of FACT in DNA replication, we examined the rates of DNA replication elongation (Fig. 4) and initiation (Fig. 5), the amounts DNA replication enzymes/factors (Fig. 6), and nucleosome assembly activity on newly synthesized daughter strands (Fig. 7) under dysfunctional FACT conditions (Figs. 1 and 2)

Read more

Summary

Introduction

Ordered nucleosome disassembly and reassembly are required for eukaryotic DNA replication. To elucidate the functional role of FACT in replication fork progression during DNA elongation in the cells, we generated and analyzed conditional SSRP1 gene knock-out chicken (Gallus gallus) DT40 cells.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call