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. 2005 Apr 18;201(8):1191–1196. doi: 10.1084/jem.20050292

Table II.

Pattern of nucleotide changes in JH4 intronic sequences of normal, polη-, and MSH2-deficient mice

Within G/C
Within A/T
Trans.
Transv.
Trans.
Transv.
GC:AT Transitions:
transversions
G/AC/T G/TC/A G/CC/G A/GT/C A/TT/A A/CT/G
Mouse
Controls 1a 44.3:55.7 53.7:46.3 61.4 18.5 20.1 47.6 26.2 26.2
Controls 1b 49.9:50.1 53.3:46.7 54.5 16.8 28.7 52.1 25.9 22.0
Polη−/− c 85.5:14.5 51.3:48.7 57.1 12.7 30.2 17.2 26.2 56.2
Msh2 −/− d 87.0:13.0 71.2:28.8 74.0 14.0 12.0 52.7 25.7 21.6
Human
Controls 1e 46.0:54.0 51.2:48.8 55.4 16.5 28.1 47.6 25.0 27.4
XP-V e 89.3:10.7 46.6:53.4 51.1 17.1 31.8 9.4 36.4 54.2

Values in bold represent significant differences from controls discussed in the text.

a

This study (122 mutations).

b

From a larger sample (334 mutations; reference 36).

c

This study, data from all deficient mice together (366 mutations).

d

Data from mice deficient in the MSH2-dependent pathway (Msh2 −/−, Exo1 −/−, Msh2 G674A) were pooled (326 mutations obtained by Pfu polymerase; references 8, 11, 12).

e

From ref. 17 (168 mutations).