DNK polimeraza beta

DNK polimeraza beta
PDB prikaz baziran na 1bno​.
Dostupne strukture
1BPX​, 1BPY​, 1BPZ​, 1MQ2​, 1MQ3​, 1TV9​, 1TVA​, 1ZJM​, 1ZJN​, 1ZQA​, 1ZQB​, 1ZQC​, 1ZQD​, 1ZQE​, 1ZQF​, 1ZQG​, 1ZQH​, 1ZQI​, 1ZQJ​, 1ZQK​, 1ZQL​, 1ZQM​, 1ZQN​, 1ZQO​, 1ZQP​, 1ZQQ​, 1ZQR​, 1ZQS​, 1ZQT​, 2FMP​, 2FMQ​, 2FMS​, 2I9G​, 2ISO​, 2ISP​, 2P66​, 2PXI​, 3C2K​, 3C2L​, 3C2M​, 3GDX​, 3ISB​, 3ISC​, 3ISD​, 3JPN​, 3JPO​, 3JPP​, 3JPQ​, 3JPR​, 3JPS​, 3JPT​, 3LK9​, 3MBY​, 3OGU​, 3RH4​, 3RH5​, 3RH6​, 3RJE​, 3RJF​, 3RJG​, 3RJH​, 3RJI​, 3RJJ​, 3RJK​, 3TFR​, 3TFS​, 7ICE​, 7ICF​, 7ICG​, 7ICH​, 7ICI​, 7ICJ​, 7ICK​, 7ICL​, 7ICM​, 7ICN​, 7ICO​, 7ICP​, 7ICQ​, 7ICR​, 7ICS​, 7ICT​, 7ICU​, 7ICV​, 8ICA​, 8ICB​, 8ICC​, 8ICE​, 8ICF​, 8ICG​, 8ICH​, 8ICI​, 8ICJ​, 8ICK​, 8ICL​, 8ICM​, 8ICN​, 8ICO​, 8ICP​, 8ICQ​, 8ICR​, 8ICS​, 8ICT​, 8ICU​, 8ICV​, 8ICW​, 8ICX​, 8ICY​, 8ICZ​, 9ICA​, 9ICB​, 9ICC​, 9ICE​, 9ICF​, 9ICG​, 9ICH​, 9ICI​, 9ICJ​, 9ICK​, 9ICL​, 9ICM​, 9ICN​, 9ICO​, 9ICP​, 9ICQ​, 9ICR​, 9ICS​, 9ICT​, 9ICU​, 9ICV​, 9ICW​, 9ICX​, 9ICY
Identifikatori
Simboli POLB; MGC125976
Vanjski ID OMIM174760 MGI97740 HomoloGene2013 GeneCards: POLB Gene
EC broj 2.7.7.7
Pregled RNK izražavanja
podaci
Ortolozi
Vrsta Čovek Miš
Entrez 5423 18970
Ensembl ENSG00000070501 ENSMUSG00000031536
UniProt P06746 Q8K409
RefSeq (mRNA) NM_002690.2 NM_011130.2
RefSeq (protein) NP_002681.1 NP_035260.1
Lokacija (UCSC) Chr 8:
42.2 - 42.23 Mb
Chr 8:
23.74 - 23.76 Mb
PubMed pretraga [1] [2]
Regulatorni element u POLB
Predviđena sekundarna struktura stem loopII (M2) regulatornog elementa POLB
Identifikatori
Simbol POLB
Rfam RF01455
Entrez 5423
HUGO POLB
OMIM 174760
RefSeq NM_002690
Drugi podaci
RNK tip Cis-reg
Domain(i) Mammalia
Lokus Hromozom 8 p11.2

DNK polimeraza beta (POLB) je enzim koji kod ljudi kodira POLBgen.[1]

Funkcija

U eukariotskim ćelijama, DNK polimeraza beta (POLB) izvodi popravke ekscizijom baza (BER) koje su neophodne za popravku DNK, replikaciju, rekombinaciju, i otpornost na lekove.[1]

Regulacija ekspresije

DNK polimeraza beta održava genomski integritet putem uzimanja učešća u popravci ekscizijom baza. Prekomerno izražavanje POLB iRNK je u korelaciji sa brojnim tipovima kancera, dok deficijencije POLB-a rezultuju u hipersenzitivnosti na alkilirajuće agense, uključujući apoptozu, i prekid hromozoma.[2] Iz tih razloga, esencijalno je precizno održavanje kontrole POLB ekspresije.[3][4][5][6]

Interakcije

DNA polimeraza beta formira interakcije sa PNKP[7] i XRCC1.[8][9][10][11]

Reference

  1. ^ а б „Entrez Gene: POLB polymerase (DNA directed), beta”. 
  2. ^ Narayan S, He F, Wilson SH (1996). „Activation of the human DNA polymerase beta promoter by a DNA-alkylating agent through induced phosphorylation of cAMP response element-binding protein-1”. J. Biol. Chem. 271 (31): 18508—13. PMID 8702497. doi:10.1074/jbc.271.31.18508. 
  3. ^ Y, Canitrot; C, Cazaux; Fréchet M; et al. (1998). „Overexpression of DNA polymerase beta in cell results in a mutator phenotype and a decreased sensitivity to anticancer drugs”. Proc. Natl. Acad. Sci. U.S.A. 95 (21): 12586—90. PMC 22874Слободан приступ. PMID 9770529. doi:10.1073/pnas.95.21.12586. 
  4. ^ V, Bergoglio; MJ, Pillaire; Lacroix-Triki M; et al. (2002). „Deregulated DNA polymerase beta induces chromosome instability and tumorigenesis”. Cancer Res. 62 (12): 3511—4. PMID 12067997. 
  5. ^ V, Bergoglio; Y, Canitrot; Hogarth L; et al. (2001). „Enhanced expression and activity of DNA polymerase beta in human ovarian tumor cells: impact on sensitivity towards antitumor agents”. Oncogene. 20 (43): 6181—7. PMID 11593426. doi:10.1038/sj.onc.1204743. 
  6. ^ Srivastava DK, Husain I, Arteaga CL, Wilson SH (1999). „DNA polymerase beta expression differences in selected human tumors and cell lines”. Carcinogenesis. 20 (6): 1049—54. PMID 10357787. doi:10.1093/carcin/20.6.1049. 
  7. ^ Whitehouse, C J; Taylor R M; Thistlethwaite A; Zhang H; Karimi-Busheri F; Lasko D D, Weinfeld M; Caldecott K W (2001). „XRCC1 stimulates human polynucleotide kinase activity at damaged DNA termini and accelerates DNA single-strand break repair”. Cell. United States. 104 (1): 107—17. ISSN 0092-8674. PMID 11163244. doi:10.1016/S0092-8674(01)00195-7. 
  8. ^ Wang, Liming; Bhattacharyya Nandan; Chelsea Diane M; Escobar Pedro F, Banerjee Sipra (2004). „A novel nuclear protein, MGC5306 interacts with DNA polymerase beta and has a potential role in cellular phenotype”. Cancer Res. United States. 64 (21): 7673—7. ISSN 0008-5472. PMID 15520167. doi:10.1158/0008-5472.CAN-04-2801. 
  9. ^ Fan, Jinshui; Otterlei Marit (2004). „XRCC1 co-localizes and physically interacts with PCNA”. Nucleic Acids Res. England. 32 (7): 2193—201. PMC 407833Слободан приступ. PMID 15107487. doi:10.1093/nar/gkh556. 
  10. ^ Kubota, Y; Nash R A (1996). „Reconstitution of DNA base excision-repair with purified human proteins: interaction between DNA polymerase beta and the XRCC1 protein”. EMBO J. ENGLAND. 15 (23): 6662—70. ISSN 0261-4189. PMC 452490Слободан приступ. PMID 8978692. 
  11. ^ Bhattacharyya, N; Banerjee S (2001). „A novel role of XRCC1 in the functions of a DNA polymerase beta variant”. Biochemistry. United States. 40 (30): 9005—13. ISSN 0006-2960. PMID 11467963. doi:10.1021/bi0028789. 

Literatura

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