Molecular Mechanism of Telomerase Action

Project: Research project

Project Details


Telomerase is a specialized reverse transcriptase (RT) that synthesizes telomere DNA repeats at chromosome ends, using only a very short region of its intrinsic telomerase RNA (TR) subunit as template. This highly specialized function of telomerase relies on a special mechanism whereby the template RNA and the telomeric DNA dissociate and realign during the processive synthesis of repeats. However, the detailed mechanism of telomerase template translocation remains to be determined. This research program aims to articulate the unique mechanism of telomerase action and identify elements that regulate specific steps of template translocation. Although telomerase uses the single-stranded telomeric DNA as its native substrate, we have recently discovered that telomerase can act as a conventional RT utilizing RNA/DNA duplex as substrate. More surprisingly, telomerase recognizes the duplex substrate with a sequence-specificity. These crucial findings have provided great insights into the molecular mechanism of telomerase action. We hypothesize that duplex-binding and duplex-dissociation are important steps of the telomere-repeat synthesis cycle, and regulate telomere-repeat addition rate and processivity. Specific Aims of the research program include (1) Determining the role duplex-binding affinity in template translocation efficiency, (2) Determining the rate-limiting step of template translocation, and (3) characterize the sequence-dependent termination of nucleotide addition by telomerase. We expect the outcomes of these experiments will greatly add to our understanding of telomerase mechanism.


The long-term objective of this work is to understand the biochemical mechanism of the telomerase enzyme. Telomerase is a highly specialized reverse transcriptase (RT), responsible for the maintenance of the telomeric ends capping linear eukaryotic chromosomes. This is wholly essential for genome stability and central to human cellular aging, cancer biology and disease.

Telomerase synthesizes telomeric DNA repeats by reverse transcribing a precisely defined short template within the vastly larger internal telomerase RNA (TR) component. For human telomerase, we have recently reported that the TR template self-defines its boundary through an exceptionally unusual mechanism, whereby telomerase recognizes a single-nucleotide embedded in the DNA product to terminate DNA synthesis at the end of the template. We will build on this exciting discovery by investigating the mechanism for which this pause signal is recognized and facilities the complex telomerase catalytic cycle.

Beyond merely providing the RNA template for DNA synthesis, the TR component contains essential and evolutionarily conserved RNA structural domains: the pseudoknot and CR4/5. The catalytic telomerase RT (TERT) protein component contains the hallmark RT motifs that constitute the catalytic site for DNA synthesis. However, the TERT protein is absolutely reliant on pseudoknot and CR4/5 association for catalytic activity. Disease mutations that damage these critical RNA domains within TR abolish TERT protein activity. The mechanism underlying TERT reliance on TR for functionality has remained elusive until our recent breakthrough with the mapping the TERT-CR4/5 binding interface has directly lead to the testable hypothesis of CR4/5 acting as an allosteric regulator. We are now well positioned to interrogate the mechanism for CR4/5, and map the TERT-pseudoknot binding interface, to reveal their precise functionality.

This research project focuses on illuminating the molecular mechanisms of telomerase function, encompassing both the unique telomerase-specific phenomenon of sequence-dependent pausing and the absolute reliance on RNA components for TERT protein catalysis. We will employ state-of-the-art systems and innovative assays that we have pioneered and established for dissecting specific telomerase catalytic steps, mapping TERT-TR binding interface(s) and articulating detailed TR domain functionality. The Specific Aims of the research project include (1) determining the underlying mechanism of telomerase sequence-dependent pausing, (2) ascertaining the allosteric functional role of the CR4/5 domain, and (3) mapping the binding interface between the TERT protein and the TR pseudoknot domain for functional analysis. The highly specialized and unique function of the telomerase enzyme requires high-level synergy among the myriad of domains comprising the TERT and TR components. Successful outcomes of these aims will provide much-needed details necessary for understanding the complex inner workings of telomerase action.


This administrative supplement request is in response to NOT-GM-19-013, Notice of Availability of Administrative Supplements for Equipment Purchases for NIGMS Awardees, for the purchase of an AKTA pure 25M FPLC system. These administrative supplement funds will allow the purchase of an instrument essential for the purification of the telomerase enzyme and recombinant proteins. This new instrument will replace a nonfunctional instrument in the sponsored laboratory at Arizona State University and expedite the progress of the proposed research projects.
Effective start/end date7/1/166/30/21


  • HHS-NIH: National Institute of General Medical Sciences (NIGMS): $1,334,737.00


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