TopBP1 controls BLM protein level to maintain genome stability.

Abstract

Human TopBP1 is a key mediator protein involved in DNA replication checkpoint control. In this study, we report a specific interaction between TopBP1 and Bloom syndrome helicase (BLM) that is phosphorylation and cell-cycle dependent. Interestingly, TopBP1 depletion led to decreased BLM protein level and increased sister chromatid exchange (SCE). Moreover, our data indicated that BLM was ubiquitinated by E3 ligase MIB1 and degraded in G1 cells but was stabilized by TopBP1 in S phase cells. Depletion of MIB1 restored BLM protein level and rescued the elevated SCE phenotype in TopBP1-depleted cells. In addition, cells expressing an undegradable BLM mutant showed radiation sensitivity, probably by triggering end resection and inhibiting the nonhomologous end-joining (NHEJ) pathway in G1 phase. Altogether, these data suggest that, although BLM is downregulated in G1 phase in order to promote NHEJ-mediated DNA repair, it is stabilized by TopBP1 in S phase cells in order to suppress SCE and thereby prevent genomic instability.

• Authors: Jiadong Wang, Junjie Chen, Zihua Gong
• Journal: Molecular cell (Mol Cell) Vol. 52 Issue 5 Pg. 667-78 (Dec 12 2013) ISSN: 1097-4164 [Electronic] United States
• PMID: 24239288 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, Non-P.H.S.)
• Copyright: Copyright © 2013 Elsevier Inc. All rights reserved.

Chemical References

• Carrier Proteins
• DNA-Binding Proteins
• Nuclear Proteins
• TOPBP1 protein, human
• MIB1 ligase, human
• Ubiquitin-Protein Ligases
• Bloom syndrome protein
• RecQ Helicases

Topics

• Carrier Proteins (genetics, metabolism)
• Cell Line
• Cell Line, Tumor
• DNA End-Joining Repair
• DNA-Binding Proteins (genetics, metabolism)
• Down-Regulation
• G1 Phase (genetics)
• Genomic Instability
• HEK293 Cells
• HeLa Cells
• Humans
• Nuclear Proteins (genetics, metabolism)
• Phosphorylation
• RecQ Helicases (genetics, metabolism)
• S Phase (genetics)
• Sister Chromatid Exchange
• Ubiquitin-Protein Ligases (genetics, metabolism)