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The rs115160714 TopBP1 may be a genetic marker of etiology and progression in laryngeal cancer.
The innate immune regulator STAT-5 is shown to regulate transcription of the ATR binding factor TopBP1, and this is critical for the induction of the ATR pathway in human papillomavirus-infected keratinocytes.
TOPBP1 physically binds PLK1 (显示 PLK1 ELISA试剂盒) and promotes PLK1 (显示 PLK1 ELISA试剂盒) kinase-mediated phosphorylation of RAD51 (显示 RAD51 ELISA试剂盒) at serine 14, a modification required for RAD51 (显示 RAD51 ELISA试剂盒) recruitment to chromatin.
Functional analyses indicat that the expression TopBP1 and Claspin (显示 CLSPN ELISA试剂盒) positively affects the survival of brain cancer cells after exposure to radiation.
TopBP1 interacts with BLM to maintain genome stability but is dispensable for preventing BLM degradation.Crucial residues mediating TopBP1-MDC1 (显示 MDC1 ELISA试剂盒) interactions identified.
TopBP1 maintains genome integrity in mitosis by controlling chromatin recruitment of SLX4 (显示 BTBD12 ELISA试剂盒) and by facilitating unscheduled DNA synthesis.
Findings demonstrate that TopBP1 and ATR are able to inhibit the synthesis of rRNA and to activate nucleolar stress pathway.
TOPBP1 has a role in recruiting TOP2A (显示 TOP2A ELISA试剂盒) to ultra-fine anaphase bridges to aid in their resolution
The results suggest that interactions between TopBP1 and E2 and between Brd4 (显示 BRD4 ELISA试剂盒) and E2 are required to correctly initiate human papillomavirus 16 DNA replication but are not required for continuing DNA replication.
Phosphorylation of BRIT1 protein coordinates TopBP1 protein recruitment and amplifies ATR signaling in cell DNA damage.
Consistent with prior reports, TopBP1 co-localized in discrete nuclear foci and was in complex with papillomavirus E2 protein (显示 UBE2B ELISA试剂盒).
The deacetylated form of TopBP1 in SIRT1 (显示 SIRT1 ELISA试剂盒) mutant cells repressed replication origin firing, while the acetylated form of TopBP1 lost this function.
Studies identify the SIRT1 (显示 SIRT1 ELISA试剂盒)-TopBP1 axis as a key signaling mode in the regulation of the metabolic checkpoint and the DNA damage checkpoint.
TopBP1 is a crucial factor in V(D)J rearrangement during the development of B, T and iNKT cells.
Our data suggest that, unlike the yeast models, the TopBP1-AAD is the major activator of ATR, sustaining cell proliferation and embryonic development
TopBP1 is crucial for maintaining genome integrity in the early progenitors that drive neurogenesis.
Tethering DNA damage checkpoint mediator proteins topoisomerase IIbeta-binding protein 1 (TopBP1) and Claspin (显示 CLSPN ELISA试剂盒) to DNA activates ataxia-telangiectasia mutated and RAD3-related (ATR (显示 ATR ELISA试剂盒)) phosphorylation of checkpoint kinase 1 (Chk1 (显示 CHEK1 ELISA试剂盒)).
TopBP1 deficiency in untransformed mouse and human primary cells induces cellular senescence rather than apoptosis. These results indicate that TopBP1 is essential for cell proliferation and maintenance of chromosomal integrity.
ATR (显示 ATR ELISA试剂盒) and TopBP1 monitor meiotic recombination and are required for activation of the meiotic recombination checkpoint
TopBP1 is a c-Abl-interacting protein and a repressor for c-Abl expression
Data show that TopBP1 and Nbs1 (显示 NLRP2 ELISA试剂盒) associate with the N-terminal region of Mdc1 (显示 MDC1 ELISA试剂盒) in egg extracts.
The critical ATR (显示 ATR ELISA试剂盒) activator, TopBP1, senses DNA damage and stalled replication forks to initiate assembly of checkpoint signaling complexes.
TopBP1's C-terminal motif containing a putative nuclear localization signal was required for Importin beta (显示 KPNB1 ELISA试剂盒) interaction and that CT100 of Importin beta (显示 KPNB1 ELISA试剂盒) was required for TopBP1 interaction.
these findings indicate that WDR18 (显示 WDR18 ELISA试剂盒) is a bona fide checkpoint protein and that WDR18 (显示 WDR18 ELISA试剂盒) works together with TopBP1 to promote DNA damage checkpoint signaling.
MRN (MRE11 (显示 MRE11A ELISA试剂盒)-RAD50 (显示 RAD50 ELISA试剂盒)-NBS1 (显示 NLRP2 ELISA试剂盒)) complex has role in ATR (显示 ATR ELISA试剂盒) activation via TOPBP1 recruitment.
Cut5 plays an integral role in the recruitment and assembly of the Chk1 (显示 CHEK1 ELISA试剂盒) signaling cascade components following DNA damage
Data show that Rad17 (显示 RAD17 ELISA试剂盒) mediates the interaction of the Rad9 (显示 RAD9A ELISA试剂盒)-Hus1 (显示 HUS1 ELISA试剂盒)-Rad1 (显示 ERCC4 ELISA试剂盒) (9-1-1) complex with the ATR (显示 ATR ELISA试剂盒)-activating protein TopBP1 in Xenopus egg extracts.
Data show that recombinant TopBP1 induces a large increase in the kinase activity of both Xenopus and human ATR (显示 ATR ELISA试剂盒)-ATRIP (显示 ATRIP ELISA试剂盒).
GEMC1 promotes initiation of chromosomal DNA replication in multicellular organisms by mediating TopBP1- and Cdk2-dependent recruitment of Cdc45 onto replication origins.
Cut5 plays a crucial role in the initial amplification step of the ATR (显示 ATR ELISA试剂盒)-Chk1 (显示 CHEK1 ELISA试剂盒) signaling pathway at the stalled replication fork.
This gene encodes a binding protein which interacts with the C-terminal region of topoisomerase II beta. This interaction suggests a supportive role for this protein in the catalytic reactions of topoisomerase II beta through transient breakages of DNA strands.
DNA topoisomerase 2-binding protein 1
, topoisomerase (DNA) II beta binding protein
, topoisomerase (DNA) II binding protein 1
, dna topoisomerase ii binding protein 1 (IC)
, DNA topoisomerase 2-binding protein 1-like
, DNA topoisomerase II-beta-binding protein 1
, DNA topoisomerase II-binding protein 1
, Cut5-related protein
, DNA topoisomerase 2-binding protein 1-A
, DNA topoisomerase 2-binding protein 1-B
, DNA topoisomerase II-binding protein 1-A
, DNA topoisomerase II-binding protein 1-B