ERCC6 Antibody

1. Case Reports: Cockayne Syndrome patients with a novel splice site ERCC6 mutation (c.2382+2T>G), and a previously described nonsense ERCC6 mutation (c.3259C>T, p.Arg1087X) in a biallelic state. PMID: 29944916
2. CSB interacts via its newly identified winged helix domain with RIF1, an effector of 53BP1, and that this interaction mediates CSB recruitment to DSBs in S phase. At double strand breaks, CSB remodels chromatin by evicting histones, which limits RIF1 and its effector MAD2L2 but promotes BRCA1 accumulation. PMID: 29203878
3. UV-induced dissociation of CSB domain interactions is a necessary step in repairing UV-induced DNA damage and that the WHD (winged helix domain) of CSB plays a key role in this dissociation. PMID: 29957539
4. CSB recruitment to DSBs is dependent upon an interaction between CSB's newly described winged-helix domain and the NHEJ factor RIF1, but subsequent remodelling activity undertaken by CSB following DSB induction inhibits RIF1 accumulation while promoting BRCA1-mediated HR repair. In vivo remodelling assays are used to demonstrate that CSB evicts histones following generation of DSBs in a manner controlled by ATM and CDK1. PMID: 29203878
5. CSB regulates double strand break repair choice by recruiting HR factors BRCA1, RPA and Rad51 while suppressing NHEJ factors at damaged chromatin in S/G2 cells. Loss of CSB impairs activation of ATM and downstream targets following induction of double strand breaks, and promotes premature exit from the G2/M checkpoint. PMID: 25820262
6. ERCC6 rs1917799, ERCC8 rs158572 and rs158916 demonstrated pairwise epistatic interactions to associate with chronic atrophic gastritis and gastric cancer risk. The ERCC6 rs1917799-ERCC8 rs158572 pair significantly influence ERCC6 and ERCC6-ERCC8 expression. PMID: 28562347
7. Let-7c-5p acted as a tumor suppressor in breast cancer possibly by negatively regulating ERCC6. PMID: 28731186
8. Loss of Cockayne syndrome group A protein (CSA) or Cockayne syndrome group B protein (CSB) leads to polymerase stalling at non-B DNA in a neuroblastoma cell line, in particular at G-quadruplex structures. PMID: 27791127
9. The present study reported two novel causative mutations on ERCC6 loci, and the clinical characteristics are described. These results add to clinical and molecular data for elucidating genotype-phenotype correlations in CS PMID: 28440418
10. Gene analysis showed mutations in exons 4 and 18 of the ERCC6 gene. Multiple ocular abnormalities were observed in a patient with Cockayne syndrome. A detailed ophthalmic evaluation of children with Cockayne syndrome is advised. PMID: 27186691
11. The role of ERCC6 in regulating response to 5-fluorouracil and drug resistance in colorectal cancer.Elevated expression of ERCC6 is associated with poor colorectal cancer patient survival. PMID: 28665687
12. NAP1L1 increases CSB processivity by decreasing the pausing probability during translocation. Our study, therefore, uncovers the different steps of CSB-mediated chromatin remodeling that can be regulated by NAP1L1. PMID: 28369616
13. pro-apoptotic effects observed after CSB ablation PMID: 28253359
14. the Elongin A ubiquitin ligase and the CSB protein function together in a common pathway in response to Pol II stalling and DNA damage PMID: 28292928
15. The discovery has been described that G1/G0 cells exhibit Cockayne syndrome B-dependent assembly of homologous recombination factors at double strand break sites within actively transcribed regions. (Review) PMID: 27233112
16. No significant association exists between ERCC6 polymorphisms and bladder cancer risk. PMID: 27791261
17. CSB plays a role in the homeostasis and function of human neurons. CSB-deficient neural networks displayed altered electrophysiological activity, including decreased synchrony, and reduced synapse density. PMID: 26755826
18. Study found that ERCC6 transcription may be epigenetically regulated in lens epithelial cells of age-related nuclear cataract leading to its repression. PMID: 27231489
19. Mutation of Cockayne syndrome B (CSB) affects neuronal gene expression and differentiation, so we attempted to bypass its function by expressing downstream target genes. PMID: 26972010
20. new role of VCP/p97 segregase in the timely processing of ubiquitinated CSB from damaged chromatin. PMID: 26826127
21. CSB and CTCF can regulate each other's chromatin association, thereby modulating chromatin structure and coordinating gene expression in response to oxidative stress. PMID: 26578602
22. Transcription inhibition reduced accumulation of CSB at sites of monoadducts and interstrand crosslinks, but it did not affect recruitment to (although slightly affected retention at) oxidative DNA damage. PMID: 26616585
23. Data suggest that both the most C-terminal region and SUMOylation of a lysine residue in N-terminal region are important for functions of CSB/ERCC6 in transcription-coupled nucleotide excision repair following DNA breakage from UV light. PMID: 26620705
24. ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination. This report expands the disease spectrum associated with ERCC6 mutations. PMID: 25251875
25. 33 proteins that were not previously known to interact with CSB. PMID: 26030138
26. Data indicate that Cockayne syndrome group B protein CSB function is necessary for the recruitment of recombinational factors. PMID: 26100862
27. These studies have provided significant functional and mechanistic insights of Rad26p/CSB in regulation of gene expression and genome integrity as described here. PMID: 25484185
28. The present report describes a case of Cockayne syndrome in a Chinese family, with the patients carrying two missense mutations (c.1595A>G, p.Asp532Gly and c.1607T>G, p.Leu536Trp) in the ERCC6 gene in an apparently compound heterozygote. PMID: 25463447
29. new splicing ERCC6 defect causal of Cockayne syndrome. PMID: 25376329
30. Data indicate that Cockayne syndrome group B protein CSB is required for transdifferentiation of fibroblasts to neurons. PMID: 25249633
31. CSB-mutated cells, but not UVSSA-deficient cells, have increased levels of intramitochondrial reactive oxygen species (ROS), especially when mitochondrial complex I is inhibited by rotenone. PMID: 25136123
32. CSB has a crucial role in coordinated regulation of transcription and chromatin remodeling activities that are required during neurogenesis. PMID: 24874740
33. An interaction effect of pri-let-7a-1 rs10739971 polymorphism with ERCC6 rs1917799 polymorphism was observed for the risk of gastric cancer. PMID: 24586594
34. Decreased CSB occupancy of TPA-response elements when c-Jun levels were diminished. PMID: 24743307
35. CSB protein stimulates NEIL2 DNA glycosylase activity PMID: 24406253
36. ERCC6 rs1917799 polymorphism is associated with gastric cancer risk. PMID: 24289633
37. Double heterozygote for mutations of ERCC6 is associated with Cockayne syndrome. PMID: 24928003
38. Mitochondrial CSA and CSB: protein interactions and protection from ageing associated DNA mutations. PMID: 23562423
39. The role of CSA and CSB protein in the oxidative stress response. PMID: 23562424
40. CSB has been shown to regulate processes such as the transcriptional recovery after DNA damage, the p53 transcriptional response, the response to hypoxia, the response IGF-1, transactivation of nuclear receptors, transcription of housekeeping genes PMID: 23562425
41. Structure, function and regulation of CSB PMID: 23422418
42. The review focuses on the participation of the CSB and CSA proteins in many different protein interactions and complexes, and how these interactions inform us about pathways that are defective in the disease. PMID: 23583689
43. CSB and PCAF play cooperative roles to establish the active state of rRNA genes by histone acetylation PMID: 23667505
44. In CSB-deficient cells ATF3 remains bound to the promoter, thereby preventing the arrival of polymerase II and the restart of transcription. PMID: 23733932
45. In tumor cell lines, CSB is overexpressed and controls cell proliferation and apoptosis. PMID: 23419237
46. CSB modulates the CPT-induced formation of discrete p53-binding protein 1 (53BP1) nuclear foci at sites of transcription-mediated DNA strand breaks PMID: 23229313
47. Eighteen polymorphisms in four DNA repair genes were genotyped in 789 age related cataract patients and 531 normal controls from the Jiangsu Eye Study. PMID: 23322570
48. Involvement of CSB and XPC in the repair of oxidative DNA lesions independent of the remainder of the nucleotide excision repair reaction. PMID: 23253478
49. Patient-derived CSB-deficient cells exhibited a defect in efficient mitochondrial transcript production and that CSB specifically promoted elongation by the mitochondrial RNA polymerase in vitro. PMID: 22743267
50. CSB-PGBD3 fusion protein is important in both health and disease, and could play a role in Cockayne syndrome. PMID: 22483866

Show More

Hide All

HGNC: 3438

OMIM: 133540

KEGG: hsa:2074

STRING: 9606.ENSP00000348089

UniGene: Hs.49063