Many studies revealed that poly(ADP-ribose) polymerase (Pare) is involved in DNA-damage recovery, cell-death induction and maintenance of genomic stability. We generated mouse
Parp+/- embryonic stem (ES) cell lines by disrupting one allele of
Parp exon 1 with a neomycin-resistance gene-cassette and subsequently produced
Parp-/- ES cells by disrupting the remaining allele with a puromycin-resistance genecassette. Parp activity was decreased to half in
Parp+/- ES cell clones and lost in
Parp-/- ES cell clones. Growth rates of
Parp+/- and
Parp-/- ES cell clones were similar to that of parental J1 ES cells, indicating that Parp is not required for ES cell proliferation. These
Parp-/- ES cells will be useful to study biological role of poly(ADP-ribosyl)ation reaction.
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