Summary information and primary citation
- PDB-id
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2jpz;
DSSR-derived features in text and
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- Class
- DNA
- Method
- NMR
- Summary
- Human telomere DNA quadruplex structure in k+ solution
hybrid-2 form
- Reference
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Dai J, Carver M, Punchihewa C, Jones RA, Yang D (2007):
"Structure
of the Hybrid-2 type intramolecular human telomeric
G-quadruplex in K+ solution: insights into structure
polymorphism of the human telomeric sequence."
Nucleic Acids Res., 35,
4927-4940. doi: 10.1093/nar/gkm522.
- Abstract
- Formation of the G-quadruplex in the human telomeric
sequence can inhibit the activity of telomerase, thus the
intramolecular telomeric G-quadruplexes have been
considered as an attractive anticancer target. Information
of intramolecular telomeric G-quadruplex structures formed
under physiological conditions is important for
structure-based drug design. Here, we report the first
structure of the major intramolecular G-quadruplex formed
in a native, non-modified human telomeric sequence in K(+)
solution. This is a hybrid-type mixed
parallel/antiparallel-G-stranded G-quadruplex, one end of
which is covered by a novel T:A:T triple capping structure.
This structure (Hybrid-2) and the previously reported
Hybrid-1 structure differ in their loop arrangements,
strand orientations and capping structures. The distinct
capping structures appear to be crucial for the favored
formation of the specific hybrid-type intramolecular
telomeric G-quadruplexes, and may provide specific binding
sites for drug targeting. Our study also shows that while
the hybrid-type G-quadruplexes appear to be the major
conformations in K(+) solution, human telomeric sequences
are always in equilibrium between Hybrid-1 and Hybrid-2
structures, which is largely determined by the 3'-flanking
sequence. Furthermore, both hybrid-type G-quadruplexes
suggest a straightforward means for multimer formation with
effective packing in the human telomeric sequence and
provide important implications for drug targeting of
G-quadruplexes in human telomeres.