The capacity to rectify DNA double-strand breaks (DSBs) is crucial for the survival of all species. DSBs can be repaired either by homologous recombination (HR) or non-homologous end joining (NHEJ). The long-standing notion that bacteria rely solely on HR for DSB repair has been overturned by evidence that mycobacteria and other genera have an NHEJ system that depends on a dedicated DNA ligase, LigD, and the DNA-endbinding protein Ku. Recent studies have illuminated the role of NHEJ in protecting the bacterial chromosome against DSBs and other clastogenic stresses. There is also emerging evidence of functional crosstalk between bacterial NHEJ proteins and components of other DNA-repair pathways. Although still a young field, bacterial NHEJ promises to teach us a great deal about the nexus of DNA repair and bacterial pathogenesis.
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Univ East Anglia, Sch Biol Sci, Norwich, Norfolk, England
Univ East Anglia, Norwich Med Sch, Norwich, Norfolk, EnglandUniv East Anglia, Sch Biol Sci, Norwich, Norfolk, England
Manzar, Kamal
Betts, Meghan
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Univ East Anglia, Norwich Med Sch, Norwich, Norfolk, EnglandUniv East Anglia, Sch Biol Sci, Norwich, Norfolk, England
Betts, Meghan
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Bowater, Richard
Reddan, John
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Oakland Univ, Rochester, MI 48063 USAUniv East Anglia, Sch Biol Sci, Norwich, Norfolk, England
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CHA Univ, Dept Biochem, Sch Med, Seongnam Si, Gyeonggi Do, South Korea
CHA Univ, Dept Biomed Sci, Seongnam Si, Gyeonggi Do, South KoreaBeth Israel Deaconess Med Ctr, Dept Pathol, 330 Brookline Ave, Boston, MA 02215 USA
Kang, Youn-Jung
Yan, Catherine T.
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Beth Israel Deaconess Med Ctr, Dept Pathol, 330 Brookline Ave, Boston, MA 02215 USA
Broad Inst MIT & Harvard, Cambridge, MA 02143 USABeth Israel Deaconess Med Ctr, Dept Pathol, 330 Brookline Ave, Boston, MA 02215 USA