The pathways and outcomes of mycobacterial NHEJ depend on the structure of the broken DNA ends Journal Article
| Authors: | Aniukwu, J.; Glickman, M. S.; Shuman, S. |
| Article Title: | The pathways and outcomes of mycobacterial NHEJ depend on the structure of the broken DNA ends |
| Abstract: | Mycobacteria can repair DNA double-strand breaks (DSBs) via a nonhomologous end-joining (NHEJ) system that includes a dedicated DNA ligase (LigD) and the DNA end-binding protein Ku. Here we exploit an improved plasmid-based NHEJ assay and a collection of Mycobacterium smegmatis strains bearing deletions or mutations in Ku or the DNA ligases to interrogate the contributions of LigD's three catalytic activities (polymerase, ligase, and 3′ phosphoesterase) and structural domains (POL, LIG, and PE) to the efficiency and molecular outcomes of NHEJ in vivo. By analyzing in parallel the repair of blunt, 5′ overhang, and 3′ overhang DSBs, we discovered a novel end-joining pathway specific to breaks with 3′ overhangs that is Ku- and LigD-independent and perfectly faithful. This 3′ overhang NHEJ pathway is independent of ligases B and C; we surmise that it relies on NAD+-dependent LigA, the essential replicative ligase. We find that efficient repair of blunt and 5′ overhang DSBs depends stringently on Ku and the LigD POL domain, but not on the LigD polymerase activity, which mainly serves to promote NHEJ infidelity. The lack of an effect of PE-inactivating LigD mutations on NHEJ outcomes, especially the balance between deletions and insertions at blunt or 5′ overhang breaks, argues against LigD being the catalyst of deletion formation. Ligase-inactivating LigD mutations (or deletion of the LIG domain) have a modest impact on the efficiency of blunt and 5′ overhang DSB repair, because the strand sealing activity can be provided in trans by one of the other resident ATP-dependent ligases (likely LigC). Reliance on the backup ligase is accompanied by a drastic loss of fidelity during blunt end and 5′ overhang DSB repair. We conclude that the mechanisms of mycobacterial NHEJ are many and the outcomes depend on the initial structures of the DSBs and the available ensemble of end-processing and end-sealing components, which are not limited to Ku and LigD. © 2008 by Cold Spring Harbor Laboratory Press. |
| Keywords: | controlled study; gene mutation; gene deletion; mutation; dna-binding proteins; nonhuman; outcome assessment; protein domain; animal cell; dna repair; phosphatase; in vivo study; enzyme activity; bacterial strain; dna strand breakage; dna; double stranded dna; dna breaks, double-stranded; plasmids; dna structure; catalysis; dna primers; adenosine triphosphate; sequence homology; gene insertion; polydeoxyribonucleotide synthase; bacterial dna; corynebacterineae; dna ligase; dna ligases; ligase; mycobacterium smegmatis; double-strand breaks; liga; exodeoxyribonuclease v; antigens, nuclear; end-joining; ku |
| Journal Title: | Genes and Development |
| Volume: | 22 |
| Issue: | 4 |
| ISSN: | 0890-9369 |
| Publisher: | Cold Spring Harbor Laboratory Press |
| Date Published: | 2008-01-01 |
| Start Page: | 512 |
| End Page: | 527 |
| Language: | English |
| DOI: | 10.1101/gad.1631908 |
| PUBMED: | 18281464 |
| PROVIDER: | scopus |
| PMCID: | PMC2238672 |
| DOI/URL: | |
| Notes: | --- - "Cited By (since 1996): 22" - "Export Date: 17 November 2011" - "CODEN: GEDEE" - "Source: Scopus" |
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