TY - JOUR
T1 - DNA polymerase ζ generates tandem mutations in immunoglobulin variable regions
AU - Saribasak, Huseyin
AU - Maul, Robert W.
AU - Cao, Zheng
AU - Yang, William W.
AU - Schenten, Dominik
AU - Kracker, Sven
AU - Gearhart, Patricia J.
PY - 2012/6/4
Y1 - 2012/6/4
N2 - Low-fidelity DNA polymerases introduce nucleotide substitutions in immunoglobulin variable regions during somatic hypermutation. Although DNA polymerase (pol) η is the major low-fidelity polymerase, other DNA polymerases may also contribute. Existing data are contradictory as to whether pol ζ is involved. We reasoned that the presence of pol η may mask the contribution of pol ζ, and therefore we generated mice deficient for pol η and heterozygous for pol ζ. The frequency and spectra of hypermutation was unaltered between Polζ +/- Polη -/- and Polζ +/+ Polη -/- clones. However, there was a decrease in tandem double-base substitutions in Polζ +/- Polη -/- cells compared with Polζ +/+ Polη -/- cells, suggesting that pol ζ generates tandem mutations. Contiguous mutations are consistent with the biochemical property of pol ζ to extend a mismatch with a second mutation. The presence of this unique signature implies that pol ζ contributes to mutational synthesis in vivo. Additionally, data on tandem mutations from wild type, Polζ +/-, Polζ -/-, Ung -/-, Msh2 -/-, Msh6 -/-, and Ung -/- Msh2 -/- clones suggest that pol ζ may function in the MSH2-MSH6 pathway.
AB - Low-fidelity DNA polymerases introduce nucleotide substitutions in immunoglobulin variable regions during somatic hypermutation. Although DNA polymerase (pol) η is the major low-fidelity polymerase, other DNA polymerases may also contribute. Existing data are contradictory as to whether pol ζ is involved. We reasoned that the presence of pol η may mask the contribution of pol ζ, and therefore we generated mice deficient for pol η and heterozygous for pol ζ. The frequency and spectra of hypermutation was unaltered between Polζ +/- Polη -/- and Polζ +/+ Polη -/- clones. However, there was a decrease in tandem double-base substitutions in Polζ +/- Polη -/- cells compared with Polζ +/+ Polη -/- cells, suggesting that pol ζ generates tandem mutations. Contiguous mutations are consistent with the biochemical property of pol ζ to extend a mismatch with a second mutation. The presence of this unique signature implies that pol ζ contributes to mutational synthesis in vivo. Additionally, data on tandem mutations from wild type, Polζ +/-, Polζ -/-, Ung -/-, Msh2 -/-, Msh6 -/-, and Ung -/- Msh2 -/- clones suggest that pol ζ may function in the MSH2-MSH6 pathway.
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U2 - 10.1084/jem.20112234
DO - 10.1084/jem.20112234
M3 - Article
C2 - 22615128
AN - SCOPUS:84864309038
SN - 0022-1007
VL - 209
SP - 1075
EP - 1081
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 6
ER -