Abstract
Artemis, a member of the beta-CASP family, has been implicated in the regulation of both telomere stability and length. Prompted by this, we examined whether the other two putative DNA-binding members of this family, hSnm1A and hSnm1B, may associate with telomeres. hSnm1A was found to not interact with the telomere. Conversely, hSnm1B was found to associate with telomeres in vivo by both immunofluorescence and chromatin immunoprecipitation. Furthermore, the C terminus of hSnm1B was shown to interact with the TRF homology domain of TRF2 indicating that hSnm1B is likely recruited to the telomere via interaction with the double-stranded telomere-binding protein TRF2.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Binding Sites
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Cell Line
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Chromatin Immunoprecipitation
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DNA Repair Enzymes
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DNA-Binding Proteins / chemistry*
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DNA-Binding Proteins / genetics
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DNA-Binding Proteins / metabolism*
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Exodeoxyribonucleases
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Fluorescent Antibody Technique
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Humans
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Nuclear Proteins / chemistry*
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Nuclear Proteins / genetics
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Nuclear Proteins / metabolism*
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Peptide Mapping
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Protein Binding
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Protein Structure, Tertiary
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Recombinant Proteins / chemistry
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Recombinant Proteins / genetics
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Recombinant Proteins / metabolism
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Sequence Deletion
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TATA Box Binding Protein-Like Proteins / chemistry
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TATA Box Binding Protein-Like Proteins / genetics
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TATA Box Binding Protein-Like Proteins / metabolism
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Telomere / metabolism*
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Telomeric Repeat Binding Protein 2
Substances
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DNA-Binding Proteins
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Nuclear Proteins
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Recombinant Proteins
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TATA Box Binding Protein-Like Proteins
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TERF2 protein, human
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Telomeric Repeat Binding Protein 2
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DCLRE1B protein, human
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Exodeoxyribonucleases
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DNA Repair Enzymes