| First Author | Prasad R | Year | 2012 |
| Journal | Nucleic Acids Res | Volume | 40 |
| Issue | 22 | Pages | 11571-82 |
| PubMed ID | 23042675 | Mgi Jnum | J:200260 |
| Mgi Id | MGI:5507940 | Doi | 10.1093/nar/gks898 |
| Citation | Prasad R, et al. (2012) Pol beta associated complex and base excision repair factors in mouse fibroblasts. Nucleic Acids Res 40(22):11571-82 |
| abstractText | During mammalian base excision repair (BER) of lesion-containing DNA, it is proposed that toxic strand-break intermediates generated throughout the pathway are sequestered and passed from one step to the next until repair is complete. This stepwise process is termed substrate channeling. A working model evaluated here is that a complex of BER factors may facilitate the BER process. FLAG-tagged DNA polymerase (pol) beta was expressed in mouse fibroblasts carrying a deletion in the endogenous pol beta gene, and the cell extract was subjected to an 'affinity-capture' procedure using anti-FLAG antibody. The pol beta affinity-capture fraction (ACF) was found to contain several BER factors including polymerase-1, X-ray cross-complementing factor1-DNA ligase III and enzymes involved in processing 3'-blocked ends of BER intermediates, e.g. polynucleotide kinase and tyrosyl-DNA phosphodiesterase 1. In contrast, DNA glycosylases, apurinic/aprymidinic endonuclease 1 and flap endonuclease 1 and several other factors involved in BER were not present. Some of the BER factors in the pol beta ACF were in a multi-protein complex as observed by sucrose gradient centrifugation. The pol beta ACF was capable of substrate channeling for steps in vitro BER and was proficient in in vitro repair of substrates mimicking a 3'-blocked topoisomerase I covalent intermediate or an oxidative stress-induced 3'-blocked intermediate. |
