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Telomeres

Trends in Biochemical Sciences, 1986
Telomeres are specialized structures at the ends of eukaryotic linear chromosomes, consisting of protein-bound tandemly repeated simple DNA sequences. Telomeric DNA is unique in that it is copied from an RNA template that forms part of the enzyme, telomerase. This review discusses the synthesis and maintenance of these unusual structures.
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Telomere Neurobiology

2008
The ends of chromosomes consist of a hexanucleotide DNA repeat sequence and specialized DNA-binding and telomere-associated proteins. An enzyme activity called telomerase maintains telomere length by using an RNA template (TR) and a reverse transcriptase (TERT) to add the hexanucleotide sequence to the free chromosome end. The structure of telomeres is
Mark P, Mattson   +2 more
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Telomeres II

Experimental Gerontology, 2007
The extent and potential significance of telomere erosion, as a function of age in human tissues, is becoming increasingly apparent. In this, the second yearly review on telomeres and ageing, I review a small selection of papers published between July 2006 and June 2007.
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Telomeres in evolution and evolution of telomeres

Chromosome Research, 2005
This paper examines telomeres from an evolutionary perspective. In the monocot plant order Asparagales two evolutionary switch-points in telomere sequence are known. The first occurred when the Arabidopsis-type telomere was replaced by a telomere based on a repeat motif more typical of vertebrates. The replacement is associated with telomerase activity,
Jirí, Fajkus   +2 more
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Telomere‐associated proteins: cross‐talk between telomere maintenance and telomere‐lengthening mechanisms

The Journal of Pathology, 2009
AbstractTelomeres, the ends of eukaryotic chromosomes, have been the subject of intense investigation over the last decade. As telomere dysfunction has been associated with ageing and developing cancer, understanding the exact mechanisms regulating telomere structure and function is essential for the prevention and treatment of human cancers and age ...
De Boeck, Gitte   +3 more
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Telomeres--Unsticky Ends

Science, 1998
Cells are equipped with surveillance mechanisms that carefully scan the DNA for breaks and repair any that are found. So what happens when this quality control apparatus comes upon the end of the chromosome, the telomere? An ill-placed repair at this position will join two chromosomes together or, worse, join the end of one chromosome to internal ...
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Telomere uncapping and alternative lengthening of telomeres

Mechanisms of Ageing and Development, 2008
A substantial number of human tumors utilize a telomerase-independent telomere length maintenance mechanism referred to as alternative lengthening of telomeres (ALT). Although it is known that ALT is a telomere-specific, loss of function phenotype, which involves lengthening of telomeres by homologous recombination-mediated replication of telomeric DNA,
Anthony J, Cesare, Roger R, Reddel
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Centromeres and telomeres

Current Opinion in Cell Biology, 1992
Centromeres and telomeres are both composed of specific DNA sequences and unique chromosomal proteins. Isolation and characterization of some of these sequences and proteins has greatly increased our knowledge of centromere and telomere structure. This information is allowing us to determine how centromeres and telomeres perform their various roles in ...
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TELOMERE LENGTH REGULATION

Annual Review of Biochemistry, 1996
Telomeres are the components of chromosome ends that provide stability and allow the complete replication of the ends. Telomere length is maintained by a balance between processes that lengthen and those that shorten telomeres. Telomeraseis a ribonucleoprotein polymerase that specifically elongates telomeres.
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Human Telomeres and Telomere Biology Disorders

2014
Telomeres consist of long nucleotide repeats and a protein complex at chromosome ends essential for chromosome stability. Telomeres shorten with each cell division and thus are markers of cellular age. Dyskeratosis congenita (DC) is a cancer-prone inherited bone marrow failure syndrome caused by germ-line mutations in key telomere biology genes that ...
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