Literature DB >> 9477961

Characterization of the RNA binding properties of Ku protein.

S Yoo1, W S Dynan.   

Abstract

Ku protein, a heterodimer of 70 and 83 kDa polypeptides, is the regulatory component of the DNA-dependent protein kinase (DNA-PK). Ku protein binds to DNA ends and is essential for DNA double-strand break repair and V(D)J recombination. Although there is some evidence that Ku protein also binds RNA, its RNA binding properties have not been systematically explored. In the present study, Ku-binding RNAs were identified using systematic evolution of ligands by exponential enrichment (SELEX) technology. These RNAs were assigned to three classes based on common sequence motifs. Most of the selected RNAs bound to Ku protein with a Kd < or = 2 nM, comparable to the affinity of DNA fragments for Ku protein under similar conditions. Many of the RNAs inhibited DNA-PK activity by competing with DNA for a common binding site in Ku protein. None of several RNAs that were tested activated DNA-PK in the absence of DNA. The identification of diverse RNAs that bind avidly to Ku protein is consistent with the idea that natural RNAs may serve as modulators of DNA-PK activity. Moreover, the RNAs identified in this study may have utility as tools for experimental manipulation of DNA double-strand break repair activity in cells and cell extracts.

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Year:  1998        PMID: 9477961     DOI: 10.1021/bi972100w

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  26 in total

1.  Ku complex interacts with and stimulates the Werner protein.

Authors:  M P Cooper; A Machwe; D K Orren; R M Brosh; D Ramsden; V A Bohr
Journal:  Genes Dev       Date:  2000-04-15       Impact factor: 11.361

2.  Subnuclear localization of Ku protein: functional association with RNA polymerase II elongation sites.

Authors:  Xianming Mo; William S Dynan
Journal:  Mol Cell Biol       Date:  2002-11       Impact factor: 4.272

3.  Enhancement of extra chromosomal recombination in somatic cells by affecting the ratio of homologous recombination (HR) to non-homologous end joining (NHEJ).

Authors:  Gretchen M Zaunbrecher; Patrick W Dunne; Bashir Mir; Matthew Breen; Jorge A Piedrahita
Journal:  Anim Biotechnol       Date:  2008       Impact factor: 2.282

Review 4.  The Ku complex: recent advances and emerging roles outside of non-homologous end-joining.

Authors:  Sanna Abbasi; Gursimran Parmar; Rachel D Kelly; Nileeka Balasuriya; Caroline Schild-Poulter
Journal:  Cell Mol Life Sci       Date:  2021-04-15       Impact factor: 9.261

5.  Dynamic interaction of Y RNAs with chromatin and initiation proteins during human DNA replication.

Authors:  Alice Tianbu Zhang; Alexander R Langley; Christo P Christov; Eyemen Kheir; Thomas Shafee; Timothy J Gardiner; Torsten Krude
Journal:  J Cell Sci       Date:  2011-05-24       Impact factor: 5.285

6.  An analysis of CAF-1-interacting proteins reveals dynamic and direct interactions with the KU complex and 14-3-3 proteins.

Authors:  Maarten Hoek; Michael P Myers; Bruce Stillman
Journal:  J Biol Chem       Date:  2011-01-05       Impact factor: 5.157

Review 7.  Charity begins at home: non-coding RNA functions in DNA repair.

Authors:  Dipanjan Chowdhury; Young Eun Choi; Marie Eve Brault
Journal:  Nat Rev Mol Cell Biol       Date:  2013-02-06       Impact factor: 94.444

8.  Ku interacts with telomerase RNA to promote telomere addition at native and broken chromosome ends.

Authors:  Anne E Stellwagen; Zara W Haimberger; Joshua R Veatch; Daniel E Gottschling
Journal:  Genes Dev       Date:  2003-09-15       Impact factor: 11.361

9.  Ku heterodimer binds to both ends of the Werner protein and functional interaction occurs at the Werner N-terminus.

Authors:  Parimal Karmakar; Carey M Snowden; Dale A Ramsden; Vilhelm A Bohr
Journal:  Nucleic Acids Res       Date:  2002-08-15       Impact factor: 16.971

10.  RNA recognition by the DNA end-binding Ku heterodimer.

Authors:  Andrew B Dalby; Karen J Goodrich; Jennifer S Pfingsten; Thomas R Cech
Journal:  RNA       Date:  2013-04-22       Impact factor: 4.942

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