共 88 条
MMEJ repair of double-strand breaks (director's cut): deleted sequences and alternative endings
被引:700
作者:

McVey, Mitch
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机构:
Tufts Univ, Sackler Sch Grad Biomed Sci, Genet Program, Boston, MA 02111 USA
Tufts Univ, Dept Biol, Medford, MA 02155 USA Tufts Univ, Sackler Sch Grad Biomed Sci, Genet Program, Boston, MA 02111 USA

Lee, Sang Eun
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机构:
Univ Texas Hlth Sci Ctr San Antonio, Inst Biotechnol, Dept Mol Med, San Antonio, TX 78245 USA Tufts Univ, Sackler Sch Grad Biomed Sci, Genet Program, Boston, MA 02111 USA
机构:
[1] Tufts Univ, Sackler Sch Grad Biomed Sci, Genet Program, Boston, MA 02111 USA
[2] Tufts Univ, Dept Biol, Medford, MA 02155 USA
[3] Univ Texas Hlth Sci Ctr San Antonio, Inst Biotechnol, Dept Mol Med, San Antonio, TX 78245 USA
关键词:
D O I:
10.1016/j.tig.2008.08.007
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
DNA double-strand breaks are normal consequences of cell division and differentiation and must be repaired faithfully to maintain genome stability. Two mechanistically distinct pathways are known to efficiently repair double-strand breaks: homologous recombination and Ku-dependent non-homologous end joining. Recently, a third, less characterized repair mechanism, named microhomology-mediated end joining (MMEJ), has received increasing attention. MMEJ repairs DNA breaks via the use of substantial microhomology and always results in deletions. Furthermore, it probably contributes to oncogenic chromosome rearrangements and genetic variation in humans. Here, we summarize the genetic attributes of MMEJ from several model systems and discuss the relationship between MMEJ and 'alternative end joining'. We propose a mechanistic model for MMEJ and highlight important questions for future research.
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页码:529 / 538
页数:10
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