ERCC5 (xeroderma pigmentosum, complementation group G)
2001-05-01 Anne Stary  , Alain Sarasin   AffiliationLaboratory of Genetic Instability, Cancer, UPR2169 CNRS, Institut de Recherches sur le Cancer, 7, rue guy Moquet, BP 8, 94801 VILLEJUIF, France
Identity
HGNC
LOCATION
13q33.1
IMAGE

LEGEND
XPG (13q32-33) - Courtesy Mariano Rocchi, Resources for Molecular Cytogenetics.
LOCUSID
DNA/RNA
Description
30 kb; 15 exons (from 61 to 1074 bp) and 14 introns (250 to 5763 bp)
Transcription
Proteins
Description
xeroderma pigmentosum group G complementing factor; DNA-repair protein complementing XPG cells
Function
The XPG protein has DNA endonuclease activity without preference for damaged DNA and is responsible for the 3 incision made during Nucleotide Excision Repair (NER). At the site of a lesion NER proteins create a DNA bubble structure over a length of approximately 25 nucleotides and the XPG protein incises the damaged DNA strand 0-2 nucleotides 3 to the ssDNA-dsDNA junction. In most studies the 3-incision made by the XPG protein appeared to be performed prior to and independently of the 5-incision by XPF-ERCC1. The XPG protein is required non-enzymatically for subsequent 5=D5incision by the XPF/ERCC1 heterodimer during the NER process. Patients belonging to the XP-G complementation group clinically exhibit heterogeneous symptoms, from mild to very severe, sometimes associated with CS. XP-G cells are almost completely repair-deficient and as UV-sensitive as XP-A cells. About half of the described XPG patients exhibit also CS symptoms. In that case, the XPG protein is also involved in the transcription-coupled repair of oxidative DNA lesions.
Homology
Extensive sequence similarities, in bipartite domain A and B, to products of RAD repair genes of two yeasts, Saccharomyces cerevisae RAD2 and Schizosaccharomyces pombe RAD13
Mutations
Germinal
5 XPG sequence alterations: 3 point mutations and two small deletions
Implicated in
Entity name
xeroderma pigmentosum, XP group G / cockayne=D5s syndrome, XP/CS
Disease
Early skin tumours
Article Bibliography
| Pubmed ID | Last Year | Title | Authors |
|---|---|---|---|
| 7697716 | 1995 | Mammalian DNA nucleotide excision repair reconstituted with purified protein components. | Aboussekhra A et al |
| 11259578 | 2001 | Strong functional interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosome. | Araújo SJ et al |
| 11037299 | 2001 | Xeroderma pigmentosum and related disorders: defects in DNA repair and transcription. | Berneburg M et al |
| 9927729 | 1999 | Nucleotide excision repair 3' endonuclease XPG stimulates the activity of base excision repairenzyme thymine glycol DNA glycosylase. | Bessho T et al |
| 11104904 | 2001 | Induced mutagenic effects in the nucleotide excision repair deficient Drosophila mutant mus201(D1), expressing a truncated XPG protein. | Calléja FM et al |
| 10910954 | 2000 | Reduced expression levels of nucleotide excision repair genes in lung cancer: a case-control analysis. | Cheng L et al |
| 7651464 | 1995 | XPG protein has a structure-specific endonuclease activity. | Cloud KG et al |
| 10026181 | 1999 | Conserved residues of human XPG protein important for nuclease activity and function in nucleotide excision repair. | Constantinou A et al |
| 9020084 | 1997 | RETRACTED: Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G. | Cooper PK et al |
| 11266544 | 2001 | The human XPG gene: gene architecture, alternative splicing and single nucleotide polymorphisms. | Emmert S et al |
| 9034344 | 1997 | Open complex formation around a lesion during nucleotide excision repair provides a structure for cleavage by human XPG protein. | Evans E et al |
| 9351836 | 1997 | Mechanism of open complex and dual incision formation by human nucleotide excision repair factors. | Evans E et al |
| 9305916 | 1997 | The DNA repair endonuclease XPG binds to proliferating cell nuclear antigen (PCNA) and shares sequence elements with the PCNA-binding regions of FEN-1 and cyclin-dependent kinase inhibitor p21. | Gary R et al |
| 8078765 | 1994 | Human xeroderma pigmentosum group G gene encodes a DNA endonuclease. | Habraken Y et al |
| 8818951 | 1996 | Xeroderma pigmentosum--Cockayne syndrome complex: a further case. | Hamel BC et al |
| 10839526 | 2000 | DNA repair. The bases for Cockayne syndrome. | Hanawalt PC et al |
| 10022922 | 1999 | Postnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G gene. | Harada YN et al |
| 7700386 | 1995 | RPA involvement in the damage-recognition and incision steps of nucleotide excision repair. | He Z et al |
| 8652557 | 1996 | Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein. | Iyer N et al |
| 10024877 | 1999 | Base excision repair of oxidative DNA damage activated by XPG protein. | Klungland A et al |
| 8632779 | 1996 | Multiple nuclear localization signals in XPG nuclease. | Knauf JA et al |
| 10786832 | 2000 | Transcription-coupled repair of 8-oxoguanine: requirement for XPG, TFIIH, and CSB and implications for Cockayne syndrome. | Le Page F et al |
| 8413238 | 1993 | Human ERCC5 cDNA-cosmid complementation for excision repair and bipartite amino acid domains conserved with RAD proteins of Saccharomyces cerevisiae and Schizosaccharomyces pombe. | MacInnes MA et al |
| 8626644 | 1996 | Replication protein A confers structure-specific endonuclease activities to the XPF-ERCC1 and XPG subunits of human DNA repair excision nuclease. | Matsunaga T et al |
| 8660947 | 1996 | Roles of XPG and XPF/ERCC1 endonucleases in UV-induced immunostaining of PCNA in fibroblasts. | Miura M et al |
| 8823375 | 1996 | DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cells. | Moriwaki S et al |
| 3620347 | 1987 | Xeroderma pigmentosum complementation group G--report of two cases. | Norris PG et al |
| 10669734 | 2000 | Terminally differentiated human neurons repair transcribed genes but display attenuated global DNA repair and modulation of repair gene expression. | Nouspikel T et al |
| 8090225 | 1994 | XPG endonuclease makes the 3' incision in human DNA nucleotide excision repair. | O'Donovan A et al |
| 7504187 | 1994 | Complementation of xeroderma pigmentosum cells by microinjection of mRNA fractionated under denaturing conditions: an estimation of sizes of XP-E and XP-G mRNA. | Okuno Y et al |
| 8710877 | 1996 | Ultraviolet-induced movement of the human DNA repair protein, Xeroderma pigmentosum type G, in the nucleus. | Park MS et al |
| 9346928 | 1997 | Characterization of a putative helix-loop-helix motif in nucleotide excision repair endonuclease, XPG. | Park MS et al |
| 8088806 | 1994 | The human gene for xeroderma pigmentosum complementation group G (XPG) maps to 13q33 by fluorescence in situ hybridization. | Samec S et al |
| 8483504 | 1993 | Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2. | Scherly D et al |
| 7510366 | 1994 | An ERCC5 gene with homology to yeast RAD2 is involved in group G xeroderma pigmentosum. | Shiomi T et al |
| 9678065 | 1998 | Enhancement of XPG mRNA expression by human interferon-beta in Cockayne syndrome cells. | Sugita K et al |
| 11340641 | 2001 | Purkinje cell degeneration in mice lacking the xeroderma pigmentosum group G gene. | Sun XZ et al |
| 9864391 | 1999 | Enhancement of XPG mRNA transcription by human interferon-beta in Cockayne syndrome cells with complementation group B. | Suzuki Y et al |
| 1483924 | 1992 | Precise localization of the excision repair gene, ERCC5, to human chromosome 13q32.3-q33.1 by direct R-banding fluorescence in situ hybridization. | Takahashi E et al |
| 8317483 | 1993 | Xeroderma pigmentosum complementation group G associated with Cockayne syndrome. | Vermeulen W et al |
| 7799936 | 1995 | An XPG DNA repair defect causing mutagen hypersensitivity in mouse leukemia L1210 cells. | Vilpo JA et al |
| 9618470 | 1998 | Assembly, subunit composition, and footprint of human DNA repair excision nuclease. | Wakasugi M et al |
| 11141066 | 2001 | Novel functional interactions between nucleotide excision DNA repair proteins influencing the enzymatic activities of TFIIH, XPG, and ERCC1-XPF. | Winkler GS et al |
| 8162019 | 1994 | Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11. | Wu YQ et al |
| 11228268 | 2001 | Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy. | Zafeiriou DI et al |
| 9553721 | 1998 | Retrovirus-mediated DNA repair gene transfer into xeroderma pigmentosum cells: perspectives for a gene therapy. | Zeng L et al |
| 10891549 | 2000 | Computer based analyses of the 5'-flanking regions of selected genes involved in the nucleotide excision repair complex. | Zhong X et al |
| 10197977 | 1999 | Molecular mechanism of nucleotide excision repair. | de Laat WL et al |
Other Information
Locus ID:
NCBI: 2073
MIM: 133530
HGNC: 3437
Ensembl: ENSG00000134899
Variants:
dbSNP: 2073
ClinVar: 2073
TCGA: ENSG00000134899
COSMIC: ERCC5
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
PharmGKB
| Entity ID | Name | Type | Evidence | Association | PK | PD | PMIDs |
|---|---|---|---|---|---|---|---|
| PA150595617 | platinum | Chemical | ClinicalAnnotation | associated | PD | 22158331 | |
| PA445204 | Ovarian Neoplasms | Disease | ClinicalAnnotation | associated | PD | 22158331 |
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38285784 | 2024 | Genetic Polymorphisms of XPC, XPD, XPG Genes and their Association with Radiotherapy Induced Toxicity among Head and Neck Cancer Patients: A Hospital Based Study from Maharashtra. | 0 |
| 38285784 | 2024 | Genetic Polymorphisms of XPC, XPD, XPG Genes and their Association with Radiotherapy Induced Toxicity among Head and Neck Cancer Patients: A Hospital Based Study from Maharashtra. | 0 |
| 35691022 | 2023 | The interplay between XPG-Asp1104His polymorphism and reproductive risk factors elevates risk of breast cancer in Tanzanian women: A multiple interaction analysis. | 2 |
| 36195778 | 2023 | Elucidation of Increased Cervical Cancer Risk Due to Polymorphisms in XRCC1 (R399Q and R194W), ERCC5 (D1104H), and NQO1 (P187S). | 2 |
| 35691022 | 2023 | The interplay between XPG-Asp1104His polymorphism and reproductive risk factors elevates risk of breast cancer in Tanzanian women: A multiple interaction analysis. | 2 |
| 36195778 | 2023 | Elucidation of Increased Cervical Cancer Risk Due to Polymorphisms in XRCC1 (R399Q and R194W), ERCC5 (D1104H), and NQO1 (P187S). | 2 |
| 35780063 | 2022 | Association of nonsynonymous SNPs of nucleotide excision repair genes ERCC4 rs1800067 (G/A) and ERCC5 rs17655 (G/C) as predisposing risk factors for gallbladder cancer. | 0 |
| 35802638 | 2022 | A stable XPG protein is required for proper ribosome biogenesis: Insights on the phenotype of combinate Xeroderma Pigmentosum/Cockayne Syndrome patients. | 1 |
| 35852645 | 2022 | Variants of ERCC5 and the outcome of platinum-based regimens in non-small cell lung cancer: a prospective cohort study. | 2 |
| 35934844 | 2022 | ERCC5, HES6 and RORA are potential diagnostic markers of coronary artery disease. | 1 |
| 35780063 | 2022 | Association of nonsynonymous SNPs of nucleotide excision repair genes ERCC4 rs1800067 (G/A) and ERCC5 rs17655 (G/C) as predisposing risk factors for gallbladder cancer. | 0 |
| 35802638 | 2022 | A stable XPG protein is required for proper ribosome biogenesis: Insights on the phenotype of combinate Xeroderma Pigmentosum/Cockayne Syndrome patients. | 1 |
| 35852645 | 2022 | Variants of ERCC5 and the outcome of platinum-based regimens in non-small cell lung cancer: a prospective cohort study. | 2 |
| 35934844 | 2022 | ERCC5, HES6 and RORA are potential diagnostic markers of coronary artery disease. | 1 |
| 33219753 | 2021 | COFS type 3 in an Indian family with antenatally detected arthrogryposis. | 1 |
Citation
Anne Stary ; Alain Sarasin
ERCC5 (xeroderma pigmentosum, complementation group G)
Atlas Genet Cytogenet Oncol Haematol. 2001-05-01
Online version: http://atlasgeneticsoncology.org/gene/300/ercc5
