| Full text | |
| Author(s): |
Quinet, Annabel
;
Martins, Davi Jardim
;
Vessoni, Alexandre Teixeira
;
Biard, Denis
;
Sarasin, Alain
;
Stary, Anne
;
Martins Menck, Carlos Frederico
Total Authors: 7
|
| Document type: | Journal article |
| Source: | Nucleic Acids Research; v. 44, n. 12, p. 5717-5731, JUL 8 2016. |
| Web of Science Citations: | 10 |
| Abstract | |
Ultraviolet-induced 6-4 photoproducts (6-4PP) and cyclobutane pyrimidine dimers (CPD) can be tolerated by translesion DNA polymerases (TLS Pols) at stalled replication forks or by gap-filling. Here, we investigated the involvement of Pol eta, Rev1 and Rev3L (Pol zeta catalytic subunit) in the specific bypass of 6-4PP and CPD in repair-deficient XP-C human cells. We combined DNA fiber assay and novel methodologies for detection and quantification of single-stranded DNA (ssDNA) gaps on ongoing replication forks and postreplication repair (PRR) tracts in the human genome. We demonstrated that Rev3L, but not Rev1, is required for postreplicative gap-filling, while Pol eta and Rev1 are responsible for TLS at stalled replication forks. Moreover, specific photolyases were employed to show that in XP-C cells, CPD arrest replication forks, while 6-4PP are responsible for the generation of ssDNA gaps and PRR tracts. On the other hand, in the absence of Pol eta or Rev1, both types of lesion block replication forks progression. Altogether, the data directly show that, in the human genome, Pol eta and Rev1 bypass CPD and 6-4PP at replication forks, while only 6-4PP are also tolerated by a Pol zeta-dependent gap-filling mechanism, independent of S phase. (AU) | |
| FAPESP's process: | 14/15982-6 - Consequences of repair deficiencies in damaged genome |
| Grantee: | Carlos Frederico Martins Menck |
| Support type: | Research Projects - Thematic Grants |
| FAPESP's process: | 13/08028-1 - CEGH-CEL - Human Genome and Stem Cell Research Center |
| Grantee: | Mayana Zatz |
| Support type: | Research Grants - Research, Innovation and Dissemination Centers - RIDC |