Abstract:
:Human telomerase reverse transcriptase is an essential rate-limiting component of telomerase complex. hTERT protein in association with other proteins and the human telomerase RNA (hTR) shows telomerase activity, essential for maintaining genomic integrity in proliferating cells. hTERT binds hTR through a decapeptide located in the RID2 (RNA interactive domain 2) domain of N-terminal region. Since hTERT is essential for telomerase activity, inhibitors of hTERT are of great interest as potential anti-cancer agent. We have selected RNA aptamers against a synthetic peptide from the RID2 domain of hTERT by employing in vitro selection protocol (SELEX). The selected RNAs could bind the free peptide, as CD spectra suggested conformational change in aptamer upon RID2 binding. Extracts of cultured breast cancer cells (MCF7) expressing this aptamer showed lower telomerase activity as estimated by TRAP assay. hTERT-binding RNA aptamers hold promise as probable anti-cancer therapeutic agent.
journal_name
Mol Cell Biochemjournal_title
Molecular and cellular biochemistryauthors
Varshney A,Bala J,Santosh B,Bhaskar A,Kumar S,Yadava PKdoi
10.1007/s11010-016-2907-7subject
Has Abstractpub_date
2017-03-01 00:00:00pages
157-167issue
1-2eissn
0300-8177issn
1573-4919pii
10.1007/s11010-016-2907-7journal_volume
427pub_type
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