Telomere structures

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Telomere Structures. In mammalian cells telomere DNA contains double-stranded tandem repeats of TTAGGG followed by terminal 3 G-rich single- stranded overhangs. A previous structure of human telomerase at a resolution of 8 Å revealed a vertebrate-specific composition and architecture 3 comprising a catalytic core that is flexibly tethered to an H and ACA. Scientists are interested in understanding how telomeres are maintained because telomere shortening has been implicated in aging and telomere lengthening in cancer. Telomerase structures and regulation.

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Loss of proper telomere structure triggers severe. In this review we will bring together recent results on the structure and function of telomeres with the structural information derived from recently determined quadruplex structures formed by the G-strand and from the novel four-stranded structure formed by Abbreviations bp–base pairs. Telomeres are heterochromatic nucleoprotein structures located at the ends of linear eukaryotic chromosomes. These tasks are carried out by the telomerase holoenzyme and a unique nucleoprotein structure in which an array of telomere-associated proteins. The telomeric 3 end terminates as a single-stranded G-rich overhang able to form the t-loop in which the overhang invades the telomeric double helix remodeling the DNA into a circle. Telomeres are at the extremities of chromosome DNA.

Telomeres play an important role in cells by protecting the ends of chromosomes during DNA replication.

The interaction of TERT with TER domains is indicated grey dotted line. Targeting G-quadruplex structures at telomeres The regions of eukaryotic genomes with the highest concentration of potential G4 structures are telomeres 21 23. It consists of short nucleotide sequences which are repeated multiple times. They do not code for any protein. Schematic representation of telomere structure. The general formula for the composition of the repeating units in one strand of the telomeres of all the eukaryotes is as follows.

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Loss of proper telomere structure triggers severe. It consists of short nucleotide sequences which are repeated multiple times. On the basis of the four sstDNA-bound telomerase structures especially the highest resolution structures T3D2 and T5D5 we propose a model for telomere repeat synthesis Fig. Telomerase is a ribonucleoprotein complex composed of a reverse transcriptase enzyme catalytic subunit and a long non-coding RNA that contains the template sequence for telomere synthesis 1 2 and is required for linear chromosome maintenance in most eukaryotes. A previous structure of human telomerase at a resolution of 8 Å revealed a vertebrate-specific composition and architecture 3 comprising a catalytic core that is flexibly tethered to an H and ACA.

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Telomerase is a ribonucleoprotein complex composed of a reverse transcriptase enzyme catalytic subunit and a long non-coding RNA that contains the template sequence for telomere synthesis 1 2 and is required for linear chromosome maintenance in most eukaryotes. Telomerase is a ribonucleoprotein complex composed of a reverse transcriptase enzyme catalytic subunit and a long non-coding RNA that contains the template sequence for telomere synthesis 1 2 and is required for linear chromosome maintenance in most eukaryotes. On the basis of the four sstDNA-bound telomerase structures especially the highest resolution structures T3D2 and T5D5 we propose a model for telomere repeat synthesis Fig. The regulation of telomerase activity is of medical relevance as it has been implicated in human diseases such as cancer as well as in aging. These tasks are carried out by the telomerase holoenzyme and a unique nucleoprotein structure in which an array of telomere-associated proteins.

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Secondary structures of the Tetrahymena and human telomerase TER subunits in which regions corresponding to the pseudo-knot green template boundary element red transactivation domain blue are highlighted. Telomeres are essential nucleoprotein structures at the ends of eukaryotic chromosomes. In mammalian cells telomere DNA contains double-stranded tandem repeats of TTAGGG followed by terminal 3 G-rich single- stranded overhangs. Telomerase structures and regulation. The general formula for the composition of the repeating units in one strand of the telomeres of all the eukaryotes is as follows.

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Telomeric G4 structures have been considered as attractive anticancer targets for many years. The sequence which gets repeated varies in different species. In mammalian cells telomere DNA contains double-stranded tandem repeats of TTAGGG followed by terminal 3 G-rich single- stranded overhangs. Telomere DNA is thought to adopt the T-loop structure where the telomere end folds back on itself and the 3 G strand overhang invades into the double- stranded DNA the so-called D-loop. Scientists are interested in understanding how telomeres are maintained because telomere shortening has been implicated in aging and telomere lengthening in cancer.

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Telomeres are essential nucleoprotein structures at the ends of eukaryotic chromosomes. Telomeres allow cells to distinguish between natural chromosomal termini and double-strand breaks in the DNA and also set the lifespan of normal somatic cells by eliciting cellular senescence when they become critically short. The regulation of telomerase activity is of medical relevance as it has been implicated in human diseases such as cancer as well as in aging. On the basis of the four sstDNA-bound telomerase structures especially the highest resolution structures T3D2 and T5D5 we propose a model for telomere repeat synthesis Fig. Telomeres are present at the chromosomes terminal in all the eukaryotic organisms.

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Schematic representation of telomere structure. Loss of proper telomere structure triggers severe. It consists of short nucleotide sequences which are repeated multiple times. On the basis of the four sstDNA-bound telomerase structures especially the highest resolution structures T3D2 and T5D5 we propose a model for telomere repeat synthesis Fig. Telomerase structures and regulation.

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Telomeric G4 structures have been considered as attractive anticancer targets for many years. 5 C n AT m 384. The sequence which gets repeated varies in different species. Telomerase is a ribonucleoprotein complex composed of a reverse transcriptase enzyme catalytic subunit and a long non-coding RNA that contains the template sequence for telomere synthesis 1 2 and is required for linear chromosome maintenance in most eukaryotes. A previous structure of human telomerase at a resolution of 8 Å revealed a vertebrate-specific composition and architecture 3 comprising a catalytic core that is flexibly tethered to an H and ACA.

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Telomerase structures and regulation. Telomerase structures and regulation. Telomeric G4 structures have been considered as attractive anticancer targets for many years. These tasks are carried out by the telomerase holoenzyme and a unique nucleoprotein structure in which an array of telomere-associated proteins. A previous structure of human telomerase at a resolution of 8 Å revealed a vertebrate-specific composition and architecture 3 comprising a catalytic core that is flexibly tethered to an H and ACA.

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The regulation of telomerase activity is of medical relevance as it has been implicated in human diseases such as cancer as well as in aging. In mammalian cells telomere DNA contains double-stranded tandem repeats of TTAGGG followed by terminal 3 G-rich single- stranded overhangs. Secondary structures of the Tetrahymena and human telomerase TER subunits in which regions corresponding to the pseudo-knot green template boundary element red transactivation domain blue are highlighted. Telomeres play an important role in cells by protecting the ends of chromosomes during DNA replication. Shedding light on the chromosome end During genome replication telomerase adds repeats to the ends of chromosomes to balance the loss of telomeric DNA.

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Targeting G-quadruplex structures at telomeres The regions of eukaryotic genomes with the highest concentration of potential G4 structures are telomeres 21 23. The sequence which gets repeated varies in different species. On the basis of the four sstDNA-bound telomerase structures especially the highest resolution structures T3D2 and T5D5 we propose a model for telomere repeat synthesis Fig. In mammals maintenance of the linear chromosome ends or telomeres involves faithful replication of genetic materials and protection against DNA damage signals to ensure genome stability and integrity. In this review we will bring together recent results on the structure and function of telomeres with the structural information derived from recently determined quadruplex structures formed by the G-strand and from the novel four-stranded structure formed by Abbreviations bp–base pairs.

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The interaction of TERT with TER domains is indicated grey dotted line. A previous structure of human telomerase at a resolution of 8 Å revealed a vertebrate-specific composition and architecture 3 comprising a catalytic core that is flexibly tethered to an H and ACA. Scientists are interested in understanding how telomeres are maintained because telomere shortening has been implicated in aging and telomere lengthening in cancer. The telomeric 3 end terminates as a single-stranded G-rich overhang able to form the t-loop in which the overhang invades the telomeric double helix remodeling the DNA into a circle. Secondary structures of the Tetrahymena and human telomerase TER subunits in which regions corresponding to the pseudo-knot green template boundary element red transactivation domain blue are highlighted.

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Telomerase structures and regulation. 5 C n AT m 384. Domain structure of the telomerase RNA subunit TER. The interaction of TERT with TER domains is indicated grey dotted line. On the basis of the four sstDNA-bound telomerase structures especially the highest resolution structures T3D2 and T5D5 we propose a model for telomere repeat synthesis Fig.

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The telomeric 3 end terminates as a single-stranded G-rich overhang able to form the t-loop in which the overhang invades the telomeric double helix remodeling the DNA into a circle. Loss of proper telomere structure triggers severe. Telomere DNA is thought to adopt the T-loop structure where the telomere end folds back on itself and the 3 G strand overhang invades into the double- stranded DNA the so-called D-loop. Schematic representation of telomere structure. Telomeric G4 structures have been considered as attractive anticancer targets for many years.

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On the basis of the four sstDNA-bound telomerase structures especially the highest resolution structures T3D2 and T5D5 we propose a model for telomere repeat synthesis Fig. Telomere DNA is thought to adopt the T-loop structure where the telomere end folds back on itself and the 3 G strand overhang invades into the double- stranded DNA the so-called D-loop. Telomeres are at the extremities of chromosome DNA. Telomerase structures and regulation. The general formula for the composition of the repeating units in one strand of the telomeres of all the eukaryotes is as follows.

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Shedding light on the chromosome end During genome replication telomerase adds repeats to the ends of chromosomes to balance the loss of telomeric DNA. Telomeres allow cells to distinguish between natural chromosomal termini and double-strand breaks in the DNA and also set the lifespan of normal somatic cells by eliciting cellular senescence when they become critically short. They play several essential roles preserving genome stability and function including distinguishing chromosome ends from DNA double stranded breaks DSBs and maintenance of chromosome length. This Click Learn discusses the structure and function of telomeres. Telomeric G4 structures have been considered as attractive anticancer targets for many years.

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On the basis of the four sstDNA-bound telomerase structures especially the highest resolution structures T3D2 and T5D5 we propose a model for telomere repeat synthesis Fig. Telomerase structures and regulation. The telomeric 3 end terminates as a single-stranded G-rich overhang able to form the t-loop in which the overhang invades the telomeric double helix remodeling the DNA into a circle. Telomeres are heterochromatic nucleoprotein structures located at the ends of linear eukaryotic chromosomes. Shedding light on the chromosome end During genome replication telomerase adds repeats to the ends of chromosomes to balance the loss of telomeric DNA.

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In this review we will bring together recent results on the structure and function of telomeres with the structural information derived from recently determined quadruplex structures formed by the G-strand and from the novel four-stranded structure formed by Abbreviations bp–base pairs. Molecular genetic studies have shown that the telomere consists of several short sequences which are tandemly repeated Table 88. Targeting G-quadruplex structures at telomeres The regions of eukaryotic genomes with the highest concentration of potential G4 structures are telomeres 21 23. This Click Learn discusses the structure and function of telomeres. Shedding light on the chromosome end During genome replication telomerase adds repeats to the ends of chromosomes to balance the loss of telomeric DNA.

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Telomeres are heterochromatic nucleoprotein structures located at the ends of linear eukaryotic chromosomes. The general formula for the composition of the repeating units in one strand of the telomeres of all the eukaryotes is as follows. Telomere DNA is thought to adopt the T-loop structure where the telomere end folds back on itself and the 3 G strand overhang invades into the double- stranded DNA the so-called D-loop. Targeting G-quadruplex structures at telomeres The regions of eukaryotic genomes with the highest concentration of potential G4 structures are telomeres 21 23. These tasks are carried out by the telomerase holoenzyme and a unique nucleoprotein structure in which an array of telomere-associated proteins.

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