Transcriptomic analysis of crispr/cas9-mediated parp1-knockout cells under the influence of topotecan and tdp1 inhibitor

HIGHLIGHTS

SUMMARY

    Since PARP1 was found to be a key player in the repair of trapped TOP1cc by TDP1, the authors investigated the influence of these compounds separately and in combination with the gene_expression of the wild_type and PARP1-knockout (PARP1-KO) cells. The expression level of DNA glycosylases genes (NEIL1, SMUG1, MPG, NEIL3), and DNA_polymerases or their subunits genes (POLE4, POLD2, POLD4, POLB) decreased. DNA_polymerases δ and ε are replicative polymerases that are responsible for the synthesis of the lagging (DNA_polymerase δ), or the leading (DNA_polymerase ε) strand. FEN1 inhibits strand displacement DNA synthesis catalyzed by DNA_polymerase δ, but stimulates . . .

     

    Logo ScioWire Beta black

    If you want to have access to all the content you need to log in!

    Thanks :)

    If you don't have an account, you can create one here.

     

Scroll to Top

Add A Knowledge Base Question !

+ = Verify Human or Spambot ?