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. Author manuscript; available in PMC: 2009 Oct 1.
Published in final edited form as: DNA Repair (Amst). 2008 Aug 3;7(10):1636–1646. doi: 10.1016/j.dnarep.2008.06.008

Table 2.

DNA sequence analysis of descendants of a gap-lesion plasmid carrying a site-specific TT CPD after repair in polη-proficient and polη-deficient human cells

DNA sequence
opposite
TT CPD
Primary fibroblasts SV40-transformed
fibroblasts
Burkitt's lymphoma

POLH+/+ POLH−/− POLH+/+ POLH−/− POLH+/+ POLH−/−

Number of isolates (%)
C-AA-C 78 (99) 54 (78) 84 (94) 73 (81) 64 (89) 44 (56)
A-AA-C - 2 (3) - 1 (1) 1 (1.5) -
G-AA-C - 1 (1) - 1 (1) - -
C-CA-C - - - 1 (1) - -
C-GA-C - 3 (4) - 5 (6) - 6 (8)
C-TA-C - 2 (3) - 5 (6) - 7 (9)
C-AA-A - 2 (3) - 1 (1) - 1 (1)
Δ-AA-C - - 1 (1) - - -
C-AT-A - - - 1 (1) - -
C-TA-A - - - - 1 (1.5) -

Non-TLS events 1 (1) 5 (7) 4 (4) 2 (2) 6 (8) 20 (26)

   Total 79 (100) 69 (100) 89 (100) 90 (100) 72 (100) 78 (100)

Plasmids were extracted from kanR colonies obtained in the experiments described in Table 1, and subjected to DNA sequence analysis. The sequence opposite the site of the TT CPD is shown in the 5' to 3' direction. Accurate TLS is represented by the sequence 5'-CAAC-3'. The underlined nucleotides are those located opposite the original TT CPD. Mutations are presented by bold type. Δ represents a single-nucleotide deletion. Non-TLS events include big deletions and insertion of sequences from the control plasmid.