Special Issue DNA Repair Defects and Telomere Dysfunction in Biology Diagrams

Special Issue DNA Repair Defects and Telomere Dysfunction in Biology Diagrams The maintenance of telomere length is a prerequisite for the continuous division of cells, so telomerase is more active in cells that need to sustain division, such as tumor cells, stem cells, etc. And telomerase is specifically designed as a reverse transcriptase to resist telomere shortening. 1. Telomere structure and maintenance 1) Telomeric DNA and G-quadruplex. Telomeres are comprised of repeat sequences and bound by multiple telomeric interacting proteins. In mammalian cells, telomere DNA contains double-stranded tandem repeats of TTAGGG followed by terminal 3′ G-rich single-stranded overhangs. Telomeres are the physical ends of eukaryotic chromosomes. They protect chromosome ends from DNA degradation, recombination, and DNA end fusions, and they are important for nuclear architecture. Telomeres provide a mechanism for their replication by semiconservative DNA replication and length maintenance by telomerase.

Together these data indicate that aged C19orf43-depleted cells exhibit cohered telomeres in mitosis that are held together by RNA-DNA hybrids and are protected from DNA damage and senescence. RNaseH1 regulates TERRA-telomeric DNA hybrids and telomere maintenance in ALT tumour cells. Nat. Commun 5, 5220. 10.1038/ncomms6220. [PMC free article Mammalian telomeres are composed of TTAGGG repeats bound by a six-protein complex called shelterin. The G-rich 3′ terminating strand forms a ssDNA overhang that is also necessary for telomere maintenance because it can invade into the double-stranded telomeric DNA to form a protective structure called the t-loop [64,65]. MUS81 operates in distinct phases of the cell cycle, during S phase, MUS81 forms a complex with EME2, crucial for fork cleavage and telomere maintenance in cells dependent on the alternative

MUS81 interaction contributes to telomere maintenance ... Biology Diagrams

Dyskerin is a highly conserved, nucleolar RNA-binding protein with established roles in small nuclear ribonucleoprotein biogenesis, telomerase and telomere maintenance and precursor rRNA processing. Telomerase is functional during S phase and the bulk of rRNA maturation occurs during G 1 and S phases; both processes are inactivated during mitosis. Because NHEJ is repressed in mitosis 65, and TRF2 remains bound to deprotected mitotic telomeres to directly inhibit end-joining upon mitotic exit 29, there is no risk of telomere fusions from MAD Interestingly, ALT cancer cells and normal aged cells have another feature in common: persistent telomere cohesion. Thus, similar to tankyrase-depleted or TRF1-mutated cells, telomeres of aged and ALT cells are persistently cohered into mitosis. 15, 25, 26, 27 Persistent cohesion is a direct consequence of telomere shortening; it can be counteracted by introduction of telomerase into aged or

Given that nuclear DNA cannot be fully replicated during mitosis (i.e. end replication problem), telomeres shorten with each round of cell division, unless acted upon by different telomere