Switching and Signaling at the Telomere

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Switching and Signaling at the Telomere Elizabeth H. Blackburn  Cell  Volume 106, Issue 6, Pages 661-673 (September 2001) DOI: 10.1016/S0092-8674(01)00492-5

Figure 1 Examples of Demonstrated or Inferred Interactions among the Components of the Structural DNA-Protein Complexes Comprising the Telomeres in Budding Yeast (top) and Humans (bottom) Red line: G-rich telomeric repeat strand synthesized by telomerase (telomerase, not shown here, interacts with and extends the 3′ single-stranded overhang indicated by the arrow); green line, complementary C-rich strand of the telomeric repeats; heavy black lines, subtelomeric DNA. The 3′ terminal single-stranded telomeric DNA in human telomeres might be in alternative forms: either bound by Pot1 protein or engaged in T-loop formation. See text for further description Cell 2001 106, 661-673DOI: (10.1016/S0092-8674(01)00492-5)

Figure 2 Changes Accompanying the Cycle of Capping (telomerase-inaccessible state) and Temporary Uncapping (telomerase-accessible state) of Telomeres in Dividing Cells with Telomerase (McEachern and Blackburn, 1995) A shortened, temporarily uncapped telomeric DNA-protein complex (lower left) becomes competent for telomerase action (telomerase-accessible). The telomeric complex then becomes lengthened by telomerase (top) until it can assume a telomeric structure that is telomerase-inaccessible and therefore capped (lower right). Such capping can persist for many cell divisions even without further lengthening of the telomere by telomerase, until the telomere shortens enough to temporarily uncap again. In a normal situation, in a cell with telomerase, such temporary uncapping elicits a response involving ATM (Tel1) kinase, which acts on the telomere to render it competent for telomerase action (at least in part through phosphorylating the Rad50/Mre11/Xrs2 (NBS1) complex). See text for further description Cell 2001 106, 661-673DOI: (10.1016/S0092-8674(01)00492-5)

Figure 3 Mutually Reinforcing Mechanisms of Telomere Capping Six factors contribute to the functional and structural capping of telomeres. See text for description Cell 2001 106, 661-673DOI: (10.1016/S0092-8674(01)00492-5)

Figure 4 An Example of the Mutual Reinforcement among the Different Molecular Mechanisms that Contribute to Telomere Function Three such molecular mechanisms are depicted as legs that together support a footstool (the capped state). When only one mechanism is compromised or abrogated, such as lack of functional telomerase (middle, left) or short telomeres (middle, right), the other components of the capping system can compensate for its absence. For example, long telomeres compensate for lack of telomerase (middle, left), and telomerase can compensate for short telomeres (middle, right). Capping functions often fail only when two or more mechanisms are compromised, such as in cells with both short telomeres and no telomerase (bottom). See text for description Cell 2001 106, 661-673DOI: (10.1016/S0092-8674(01)00492-5)