Literature DB >> 14697757

Identification of DNA-PK in the arthropods. Evidence for the ancient ancestry of vertebrate non-homologous end-joining.

Andrew S Doré1, Adam C B Drake, Suzanne C Brewerton, Tom L Blundell.   

Abstract

Cellular life depends upon the preservation and transmission of genetic material. Double stranded DNA breaks (DSBs) cause catastrophic gene loss in cell division and must be promptly and accurately repaired. In eukaryotes DSBs may be repaired by either non-homologous end-joining (NHEJ), single strand annealing or homologous recombination (HR). Vertebrate NHEJ has been shown to depend upon the DNA-dependent protein kinase (DNA-PK) consisting of the phosphatidylinositol 3 (PI 3)-kinase like (PIKK) catalytic sub-unit (DNA-PKcs) and the DNA targeting factor Ku. Our analysis of recently completed genomes found several novel PIKKs in Anopheles gambiae and Drosophila melanogaster including a novel mosquito DNA-PKcs orthologue, the first non-vertebrate DNA-PKcs described to date. We also detected a DNA-PKcs fragment in the high quality EST set of Apis mellifera ligustica (honey bee) suggesting that DNA-PK is a far older and more important eukaryotic complex than previously thought.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 14697757     DOI: 10.1016/j.dnarep.2003.09.003

Source DB:  PubMed          Journal:  DNA Repair (Amst)        ISSN: 1568-7856


  10 in total

1.  In silico identification and analysis of new Artemis/Artemis-like sequences from fungal and metazoan species.

Authors:  Diego Bonatto; Martin Brendel; João Antonio Pêgas Henriques
Journal:  Protein J       Date:  2005-08       Impact factor: 2.371

2.  The Ku protein complex is involved in length regulation of Drosophila telomeres.

Authors:  Larisa Melnikova; Harald Biessmann; Pavel Georgiev
Journal:  Genetics       Date:  2005-03-21       Impact factor: 4.562

Review 3.  The DNA-dependent protein kinase: A multifunctional protein kinase with roles in DNA double strand break repair and mitosis.

Authors:  Nicholas Jette; Susan P Lees-Miller
Journal:  Prog Biophys Mol Biol       Date:  2014-12-27       Impact factor: 3.667

4.  Mutations of the Yku80 C terminus and Xrs2 FHA domain specifically block yeast nonhomologous end joining.

Authors:  Phillip L Palmbos; James M Daley; Thomas E Wilson
Journal:  Mol Cell Biol       Date:  2005-12       Impact factor: 4.272

5.  Causes and Effects of Loss of Classical Nonhomologous End Joining Pathway in Parasitic Eukaryotes.

Authors:  Anna Nenarokova; Kristína Záhonová; Marija Krasilnikova; Ondřej Gahura; Richard McCulloch; Alena Zíková; Vyacheslav Yurchenko; Julius Lukeš
Journal:  mBio       Date:  2019-07-16       Impact factor: 7.867

6.  A pathway linking translation stress to checkpoint kinase 2 signaling in Neurospora crassa.

Authors:  Axel C R Diernfellner; Linda Lauinger; Anton Shostak; Michael Brunner
Journal:  Proc Natl Acad Sci U S A       Date:  2019-08-14       Impact factor: 11.205

7.  Ku heterodimer-independent end joining in Trypanosoma brucei cell extracts relies upon sequence microhomology.

Authors:  Peter Burton; David J McBride; Jonathan M Wilkes; J David Barry; Richard McCulloch
Journal:  Eukaryot Cell       Date:  2007-08-10

8.  Uncovering DNA-PKcs ancient phylogeny, unique sequence motifs and insights for human disease.

Authors:  James P Lees-Miller; Alexander Cobban; Panagiotis Katsonis; Albino Bacolla; Susan E Tsutakawa; Michal Hammel; Katheryn Meek; Dave W Anderson; Olivier Lichtarge; John A Tainer; Susan P Lees-Miller
Journal:  Prog Biophys Mol Biol       Date:  2020-10-06       Impact factor: 4.799

Review 9.  DNA Damage Responses during the Cell Cycle: Insights from Model Organisms and Beyond.

Authors:  Delisa E Clay; Donald T Fox
Journal:  Genes (Basel)       Date:  2021-11-25       Impact factor: 4.096

Review 10.  Structural insights into the role of DNA-PK as a master regulator in NHEJ.

Authors:  Siyu Chen; James P Lees-Miller; Yuan He; Susan P Lees-Miller
Journal:  Genome Instab Dis       Date:  2021-07-23
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.