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Mre11 complex and DNA replication: linkage to E2F and sites of DNA synthesis.
Mol Cell Biol. 2001 Sep;21(17):6006-16
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A plant gene encoding a Myb-like protein that binds telomeric GGTTTAG repeats in vitro.
J Biol Chem. 2001 May 11;276(19):16511-9
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An Arabidopsis Minute-like phenotype caused by a semi-dominant mutation in a RIBOSOMAL PROTEIN S5 gene.
Development. 2001 Nov;128(21):4289-99
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Promotion of Dnl4-catalyzed DNA end-joining by the Rad50/Mre11/Xrs2 and Hdf1/Hdf2 complexes.
Mol Cell. 2001 Nov;8(5):1105-15
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Human Rad50/Mre11 is a flexible complex that can tether DNA ends.
Mol Cell. 2001 Nov;8(5):1129-35
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The plant Rad50-Mre11 protein complex.
FEBS Lett. 2002 Apr 10;516(1-3):164-6
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Telomere length deregulation and enhanced sensitivity to genotoxic stress in Arabidopsis mutants deficient in Ku70.
EMBO J. 2002 Jun 3;21(11):2819-26
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Increased telomere length and hypersensitivity to DNA damaging agents in an Arabidopsis KU70 mutant.
Nucleic Acids Res. 2002 Aug 1;30(15):3395-400
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Identification of new genes required for meiotic recombination in Saccharomyces cerevisiae.
Genetics. 1993 Jan;133(1):51-66
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Cloning and characterisation of the Schizosaccharomyces pombe rad32 gene: a gene required for repair of double strand breaks and recombination.
Nucleic Acids Res. 1995 Feb 11;23(3):383-8
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Interaction of Mre11 and Rad50: two proteins required for DNA repair and meiosis-specific double-strand break formation in Saccharomyces cerevisiae.
Genetics. 1995 Apr;139(4):1521-32
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Structural and functional similarities between the SbcCD proteins of Escherichia coli and the RAD50 and MRE11 (RAD32) recombination and repair proteins of yeast.
Mol Microbiol. 1995 Sep;17(6):1215-7
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The DNA-binding protein Hdf1p (a putative Ku homologue) is required for maintaining normal telomere length in Saccharomyces cerevisiae.
Nucleic Acids Res. 1996 Feb 15;24(4):582-5
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Cell cycle and genetic requirements of two pathways of nonhomologous end-joining repair of double-strand breaks in Saccharomyces cerevisiae.
Mol Cell Biol. 1996 May;16(5):2164-73
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Mutations in two Ku homologs define a DNA end-joining repair pathway in Saccharomyces cerevisiae.
Mol Cell Biol. 1996 Aug;16(8):4189-98
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Human Rad50 is physically associated with human Mre11: identification of a conserved multiprotein complex implicated in recombinational DNA repair.
Mol Cell Biol. 1996 Sep;16(9):4832-41
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Control of telomere length by the human telomeric protein TRF1.
Nature. 1997 Feb 20;385(6618):740-3
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Conditional gene targeted deletion by Cre recombinase demonstrates the requirement for the double-strand break repair Mre11 protein in murine embryonic stem cells.
Nucleic Acids Res. 1997 Aug 1;25(15):2985-91
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mre11S--a yeast mutation that blocks double-strand-break processing and permits nonhomologous synapsis in meiosis.
Genes Dev. 1997 Sep 1;11(17):2272-90
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Chromosome segregation during meiosis: building an unambivalent bivalent.
Curr Top Dev Biol. 1998;37:263-99
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A novel mre11 mutation impairs processing of double-strand breaks of DNA during both mitosis and meiosis.
Mol Cell Biol. 1998 Jan;18(1):260-8
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Mre11 is essential for the maintenance of chromosomal DNA in vertebrate cells.
EMBO J. 1999 Dec 1;18(23):6619-29
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T-DNA as an insertional mutagen in Arabidopsis.
Plant Cell. 1999 Dec;11(12):2283-90
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The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder.
Cell. 1999 Dec 10;99(6):577-87
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Disruption of the telomerase catalytic subunit gene from Arabidopsis inactivates telomerase and leads to a slow loss of telomeric DNA.
Proc Natl Acad Sci U S A. 1999 Dec 21;96(26):14813-8
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Control of human telomere length by TRF1 and TRF2.
Mol Cell Biol. 2000 Mar;20(5):1659-68
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Cell-cycle-regulated association of RAD50/MRE11/NBS1 with TRF2 and human telomeres.
Nat Genet. 2000 Jul;25(3):347-52
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Response to RAG-mediated VDJ cleavage by NBS1 and gamma-H2AX.
Science. 2000 Dec 8;290(5498):1962-5
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Disruption of the Arabidopsis RAD50 gene leads to plant sterility and MMS sensitivity.
Plant J. 2001 Jan;25(1):31-41
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RAD50 function is essential for telomere maintenance in Arabidopsis.
Proc Natl Acad Sci U S A. 2001 Feb 13;98(4):1711-6
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C. elegans mre-11 is required for meiotic recombination and DNA repair but is dispensable for the meiotic G(2) DNA damage checkpoint.
Genes Dev. 2001 Mar 1;15(5):522-34
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Mutations in the MRE11, RAD50, XRS2, and MRE2 genes alter chromatin configuration at meiotic DNA double-stranded break sites in premeiotic and meiotic cells.
Proc Natl Acad Sci U S A. 1998 Jan 20;95(2):646-51
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Components of the Ku-dependent non-homologous end-joining pathway are involved in telomeric length maintenance and telomeric silencing.
EMBO J. 1998 Mar 16;17(6):1819-28
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Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome.
Cell. 1998 May 1;93(3):467-76
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The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response.
Cell. 1998 May 1;93(3):477-86
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Telomere maintenance is dependent on activities required for end repair of double-strand breaks.
Curr Biol. 1998 May 21;8(11):657-60
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The 3' to 5' exonuclease activity of Mre 11 facilitates repair of DNA double-strand breaks.
Mol Cell. 1998 Jun;1(7):969-79
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Nuclease activities in a complex of human recombination and DNA repair factors Rad50, Mre11, and p95.
J Biol Chem. 1998 Aug 21;273(34):21447-50
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Alteration of N-terminal phosphoesterase signature motifs inactivates Saccharomyces cerevisiae Mre11.
Genetics. 1998 Oct;150(2):591-600
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Developmental control of telomere lengths and telomerase activity in plants.
Plant Cell. 1998 Oct;10(10):1691-8
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Distinct roles of two separable in vitro activities of yeast Mre11 in mitotic and meiotic recombination.
EMBO J. 1998 Nov 2;17(21):6412-25
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The many interfaces of Mre11.
Cell. 1998 Nov 25;95(5):583-6
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Complex formation and functional versatility of Mre11 of budding yeast in recombination.
Cell. 1998 Nov 25;95(5):705-16
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The nuclease activity of Mre11 is required for meiosis but not for mating type switching, end joining, or telomere maintenance.
Mol Cell Biol. 1999 Jan;19(1):556-66
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Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana.
Plant J. 1998 Dec;16(6):735-43
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Nbs1 potentiates ATP-driven DNA unwinding and endonuclease cleavage by the Mre11/Rad50 complex.
Genes Dev. 1999 May 15;13(10):1276-88
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The role of Schizosaccharomyces pombe Rad32, the Mre11 homologue, and other DNA damage response proteins in non-homologous end joining and telomere length maintenance.
Nucleic Acids Res. 1999 Jul 1;27(13):2655-61
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Mre11 and Ku70 interact in somatic cells, but are differentially expressed in early meiosis.
Nat Genet. 1999 Oct;23(2):194-8
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Living with genome instability: plant responses to telomere dysfunction.
Science. 2001 Mar 2;291(5509):1797-800
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Effects of DNA nonhomologous end-joining factors on telomere length and chromosomal stability in mammalian cells.
Curr Biol. 2001 Aug 7;11(15):1192-6
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