The length of telomeric G-rich strand 3′-overhang measured by oligonucleotide ligation assay
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作者:
Cimino-Reale, Graziella
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CNR, Ist Neurobiol & Med Mol, I-00137 Rome, Italy
Univ Roma La Sapienza, Dipartimento Med Sperimentale & Patol, Rome, ItalyCNR, Ist Neurobiol & Med Mol, I-00137 Rome, Italy
Cimino-Reale, Graziella
[1
,2
]
Pascale, Esterina
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Univ Aquila, Dipartimento Med Sperimentale, I-67100 Laquila, ItalyCNR, Ist Neurobiol & Med Mol, I-00137 Rome, Italy
Pascale, Esterina
[3
]
Battiloro, Eva
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CNR, Ist Neurobiol & Med Mol, I-00137 Rome, ItalyCNR, Ist Neurobiol & Med Mol, I-00137 Rome, Italy
Battiloro, Eva
[1
]
Starace, Giuseppe
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CNR, Ist Neurobiol & Med Mol, I-00137 Rome, ItalyCNR, Ist Neurobiol & Med Mol, I-00137 Rome, Italy
Starace, Giuseppe
[1
]
Verna, Roberto
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Univ Roma La Sapienza, Dipartimento Med Sperimentale & Patol, Rome, ItalyCNR, Ist Neurobiol & Med Mol, I-00137 Rome, Italy
Verna, Roberto
[2
]
D'Ambrosio, Ettore
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CNR, Ist Neurobiol & Med Mol, I-00137 Rome, ItalyCNR, Ist Neurobiol & Med Mol, I-00137 Rome, Italy
D'Ambrosio, Ettore
[1
]
机构:
[1] CNR, Ist Neurobiol & Med Mol, I-00137 Rome, Italy
[2] Univ Roma La Sapienza, Dipartimento Med Sperimentale & Patol, Rome, Italy
[3] Univ Aquila, Dipartimento Med Sperimentale, I-67100 Laquila, Italy
A typical G-rich telomeric DNA strand, which runs 5'-> 3' toward the chromosome ends, protrudes by several nucleotides in lower eukaryotes. In human chromosomes long G-rich 3'-overhangs have been found. Apart from the standard G-rich tail, several non-canonical terminal structures have been proposed. However, the mechanism of long-tail formation, the presence and the role of these structures in telomere maintenance or shortening are not completely understood. In a search for a simple method to accurately measure the 3'-overhang we have established a protocol based on the ligation of telomeric oligonucleotide hybridized to non-denatured DNA under stringent conditions (oligonucleotide ligation assay with telomeric repeat oligonucleotide). This method enabled us to detect a large proportion of G-rich single-stranded telomeric DNA that was as short as 24 nt. Nevertheless, we showed G-tails longer than 400 nt. In all tested cells the lengths ranging from 108 to 270 nt represented only 37% of the whole molecule population, while 56-62% were <90 nt. Our protocol provides a simple and sensitive method for measuring the length of naturally occurring unpaired repeated DNA.
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Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USAUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Griffith, JD
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Comeau, L
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机构:Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Comeau, L
;
Rosenfield, S
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机构:Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Rosenfield, S
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Stansel, RM
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机构:Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Stansel, RM
;
Bianchi, A
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机构:Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Bianchi, A
;
Moss, H
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机构:Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
机构:
Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USAUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Griffith, JD
;
Comeau, L
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机构:Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Comeau, L
;
Rosenfield, S
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机构:Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Rosenfield, S
;
Stansel, RM
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机构:Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Stansel, RM
;
Bianchi, A
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机构:Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Bianchi, A
;
Moss, H
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机构:Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA