Читать книгу Chemistry and Biology of Non-canonical Nucleic Acids - Naoki Sugimoto - Страница 25

As described in Chapter 1, natural DNAs form antiparallel B-type duplex, which is often designated as B-DNA, while natural RNA forms A-type duplex. It is known that DNA duplexes under conditions of low humidity and in solution in which water activity is reduced by the addition of cosolvent such as alcohols form A-type duplex (A-DNA) (Figure 2.5). X-ray diffraction analysis of oligo-DNA duplexes has demonstrated that many of the duplexes form the A-type ones, especially when their sequences have high G/C contents. However, it has been pointed out that the crystallization conditions of high alcohols commonly used in oligonucleotide crystallography may be factors that provide the A-DNA duplexes. This behavior causes a query whether the A-DNA is the functional structure in biological systems. On the other hand, structure transitions from B-DNA to A-DNA duplex have been demonstrated upon chemical and biological stimuli such as reduction of dielectric constant as one aspect of intracellular crowding condition, addition of polycationic molecule, and binding of proteins related to gene expressions [9]. The B-A transition is actually occurring in the cell nucleus, suggesting that A-DNA duplex would contribute to gene regulation in response to the molecular environment.

Figure 2.5 Structures of A-type (PDB ID: 3V9D) (a) and Z-type (PDB ID: 4OCB) (b) DNA duplexes formed in GC-rich sequence. Top views of consecutive G-C base pairs are shown above the entire structure.

DNA also form Z-type duplex (Z-DNA) (Figure 2.5). Z-DNA with the two strands forming left-handed helix shows a radically different structure from A- and B-DNAs. Phosphate backbone of Z-DNA forms a distinct zigzag pattern, which is an origin of its name, whereas that of B-DNA and A-DNA is uniformly wound to form the helix. Formation of Z-DNA depends on the oligonucleotide sequence that needs alternating purine–pyrimidine sequence such as d(GCGCGC). Guanine nucleotides in Z-DNA show C3′-end conformation in its sugar puckering and syn orientation in its glyosidic bond angle. These features place the guanine nucleobase back over the sugar ring and make the zigzag pattern in the alternating sequence. Z-DNA has a structure feature that the distance between phosphate groups at interstrand is shorter than B-DNA and A-DNA that results in stronger electrostatic repulsion. Therefore, Z-DNA needs a solution having a high salt concentration or low dielectric constant to be stabilized. It is also known that the Z-DNA is stabilized under the condition with a negative twist when the sequence is incorporated in plasmid DNA and applied in a supercoil state. The biological aspects of Z-DNA have gained more attention after the Z-DNA recognition domain has been discovered in proteins involved in gene regulation. Substantial number of Z-DNA-binding proteins has been identified in various organisms including eukaryotes, prokaryotes, and viruses [10].