ERCC8 (gene)

From Wikipedia, the free encyclopedia

Excision repair cross-complementing rodent repair deficiency, complementation group 8

Identifiers

ERCC8; CKN1; CSA

External IDs

OMIM: 609412 MGI: 1919241 HomoloGene: 62

Gene ontology
Molecular Function:	• protein binding
Cellular Component:	• nucleotide-excision repair complex • nucleus • nuclear matrix
Biological Process:	• transcription-coupled nucleotide-excision repair • transcription • regulation of transcription, DNA-dependent • sensory perception of sound

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

Refseq

NM_000082 (mRNA)
NP_000073 (protein)

NM_028042 (mRNA)
NP_082318 (protein)

Location

Chr 5: 60.21 - 60.28 Mb

Chr 13: 109.28 - 109.32 Mb

Pubmed search

[1]

[2]

Excision repair cross-complementing rodent repair deficiency, complementation group 8, also known as ERCC8, is a human gene.^[1]

This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). The CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.^[1]

[edit] References

^ ^a ^b Entrez Gene: ERCC8 excision repair cross-complementing rodent repair deficiency, complementation group 8.

[edit] Further reading

van Gool AJ, van der Horst GT, Citterio E, Hoeijmakers JH (1997). "Cockayne syndrome: defective repair of transcription?". EMBO J. 16 (14): 4155-62. PMID 9250659.
Henning KA, Li L, Iyer N, et al. (1995). "The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH.". Cell 82 (4): 555-64. PMID 7664335.
Itoh T, Shiomi T, Shiomi N, et al. (1996). "Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome complementation group A.". Mutat. Res. 362 (2): 167-74. PMID 8596535.
Bregman DB, Halaban R, van Gool AJ, et al. (1996). "UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells.". Proc. Natl. Acad. Sci. U.S.A. 93 (21): 11586-90. PMID 8876179.
Selby CP, Sancar A (1997). "Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II.". J. Biol. Chem. 272 (3): 1885-90. PMID 8999876.
Nakatsu Y, Asahina H, Citterio E, et al. (2001). "XAB2, a novel tetratricopeptide repeat protein involved in transcription-coupled DNA repair and transcription.". J. Biol. Chem. 275 (45): 34931-7. doi:10.1074/jbc.M004936200. PMID 10944529.
Kamiuchi S, Saijo M, Citterio E, et al. (2002). "Translocation of Cockayne syndrome group A protein to the nuclear matrix: possible relevance to transcription-coupled DNA repair.". Proc. Natl. Acad. Sci. U.S.A. 99 (1): 201-6. doi:10.1073/pnas.012473199. PMID 11782547.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi:10.1073/pnas.242603899. PMID 12477932.
Groisman R, Polanowska J, Kuraoka I, et al. (2003). "The ubiquitin ligase activity in the DDB2 and CSA complexes is differentially regulated by the COP9 signalosome in response to DNA damage.". Cell 113 (3): 357-67. PMID 12732143.
Cao H, Williams C, Carter M, Hegele RA (2004). "CKN1 (MIM 216400): mutations in Cockayne syndrome type A and a new common polymorphism.". J. Hum. Genet. 49 (1): 61-3. doi:10.1007/s10038-003-0107-2. PMID 14661080.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40-5. doi:10.1038/ng1285. PMID 14702039.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121-7. doi:10.1101/gr.2596504. PMID 15489334.
Ridley AJ, Colley J, Wynford-Thomas D, Jones CJ (2005). "Characterisation of novel mutations in Cockayne syndrome type A and xeroderma pigmentosum group C subjects.". J. Hum. Genet. 50 (3): 151-4. doi:10.1007/s10038-004-0228-2. PMID 15744458.
Sarker AH, Tsutakawa SE, Kostek S, et al. (2006). "Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome.". Mol. Cell 20 (2): 187-98. doi:10.1016/j.molcel.2005.09.022. PMID 16246722.
Groisman R, Kuraoka I, Chevallier O, et al. (2006). "CSA-dependent degradation of CSB by the ubiquitin-proteasome pathway establishes a link between complementation factors of the Cockayne syndrome.". Genes Dev. 20 (11): 1429-34. doi:10.1101/gad.378206. PMID 16751180.
Fousteri M, Vermeulen W, van Zeeland AA, Mullenders LH (2006). "Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo.". Mol. Cell 23 (4): 471-82. doi:10.1016/j.molcel.2006.06.029. PMID 16916636.
Saijo M, Hirai T, Ogawa A, et al. (2007). "Functional TFIIH is required for UV-induced translocation of CSA to the nuclear matrix.". Mol. Cell. Biol. 27 (7): 2538-47. doi:10.1128/MCB.01288-06. PMID 17242193.
D'Errico M, Parlanti E, Teson M, et al. (2007). "The role of CSA in the response to oxidative DNA damage in human cells.". Oncogene 26 (30): 4336-43. doi:10.1038/sj.onc.1210232. PMID 17297471.