1. TELOMERES Dr. José María Romero Romero

2. TELOMERES are specialized structures at the end of all eukaryotic chromosomes. contain longthy streches of non-coding tandemly repeated sequence, (TTAGGG)n, and specific proteins. ensure chromosome stability and protect the ends from degradation and from fusing with other chromosomes. TELOMERES:

3. TELOMERES Normal somatic cells lose telomeric repeats with ongoing cell division. Telomere length is quite important for cells because they work as a buffer avoiding the loss of coding DNA.

4. TELOMERES The loss of telomeric repeats triggers replicative senescense in cells. Telomeres sequences are extraordinary highly conserved in evolution: all vertebrates have the same simple sequence repeat.

5. TELOMERES There is an important enzyme: TELOMERASE, active only in embryonic, proliferatice cells of renewal tissues, adult male germline and cancer cells, that is the main regulator of telomere´s length. TELOMERASE is a reverse transcriptase ( a RNA- dependent polymerase) that contains an RNA with the sequence complementary to the telomere repeat TTAGGG. RNA´s polymerase is used as the template.

6. TELOMERES The model for telomeres is that they are the physical ends of linear eukaryotic chromosomes that contain up to 15 Kb of non-coding tandemly repeated sequence: (TTAGGG)n, and specific proteins, and an overhang of 50- 200 nucleotides in the chromosome terminus.

7. TELOMERES DNA Chromosome 5-15kb 30-200 nt DNA tandem repeat - (TTAGGG) n Model of a human telomere 5’ 3’

8. 3´overhang T- LOOP D-LOOP AATCCCAATCCCAA TCCCAAT TTAGGGTTAGGGTTAGGGTTA 5´ 3´ TELOMERES 5´

9. 3´overhang AATCCCAATCCCAA TCCCAAT TTAGGGTT 5´ 3´ TELOMERES 5´ 3´overhang erosion This telomere structure hasn´t stability

10. TELOMERES 5´ 3´ 3´overhang erosion Chromosomal destabilization is linked to malignancies Damaged chromosomes are degraded by nucleases and participate in end joining reactions that fuse two free ends.